Showing posts with label 2008 Survivor Stories. Show all posts
Showing posts with label 2008 Survivor Stories. Show all posts

Tuesday, February 3, 2009

Jana's Survivor Cruise















Jana Harris, our 2008 Survivor, recently took a cruise to Mexico courtesy of For Every Body and I Think Pink. She and her husband had a wonderful time together and enjoyed the beautiful weather. We were so happy to give Jana this cruise and an opportunity to celebrate life! Thanks for your example, Jana!

If you would like to nominate a breast cancer survivor you know for our 2009 awards, go to http://www.ithinkpink.org/. Nominations must be received by August 1, 2009.

Monday, August 25, 2008

Noreen's Story

What could I possibility write what has had not been written about Breast Cancer so many inspiring stories that that so many of us read and marvel at the person’s courage and strength. My story is a tale of to much reality it really isn’t all pink ribbons and races for the cure it’s about life long side effects from drugs that do allot of harm to our bodies, indifferent Doctors and hospitals the medical issues could go on and on. When you do recover from the cancer treatment society also throws many issues you way background checks that can pick up your illness if you haven’t worked a good bit of the time, no real help from job rehab every government and state agencies saying sorry I Can’t help you.

People who know about your illness, Yes folks I am one of those people who had had cancer more than once either didn’t want to look you in the eyes or they just broke down in tears. I can’t tell you how many old friends that I had to comfort. The funny thing when you are telling them you are ok they kind of want to believe you but they kind of don’t really. How could anyone not have doubts I had them myself, for to many people my illness was their worse nightmare, 37 is pretty young for Breast Cancer.

Later in my journey and talking with others in the breast cancer community I learned many get it even younger there is know certain age for breast cancer it really just isn’t your mother’s disease. The so called safety nets many in the medical community like to talk about like having children, not eating meat, exercising, and on and on don’t really make you immune. Talking with so many women in chat rooms and message boards you do find that out. They seemed betrayed they did all the things told to them still happened. My own thoughts were of course why me? What did I do to deserve this? As more and more things happened I still never got the answer to this.

What do you think when alot of the information doesn’t ring true you might ask? Well this is where the inter voice we all have comes in. I kind of call it a gift from the Creator of us all. I have found that through out my life this inter voice is my protector some would call it angel, the voice of God what ever you want to call it came early to me as you can read from my beginnings.

I was raised in the late sixties the daughter of a carpenter and a stay at home mom the youngest of 4 children. I was a cute Pixie like child who was quiet, imaginative. I dreamed of going to Africa and seeing the great cats. I loved Lions and loved to draw, and loved horses and playing with Barbie's. My sister and I were one year apart in age and shared a room in those early days in our innocence it would take decades to understand what we lived through.

Our father was a angry man, his background is one of violence against others began early in his life, fighting and stealing .He even tried the service for I guess some kind of control but even that didn’t work. This was a man who in his later years would cause such damage to the four children he gave birth to they would live with the scars for many years to come. I recall one event that is very clear still, my father was in a rage screaming and threatening all of us. Especially my mother she had decided to leave and we all went to get into the car. Running out of the house as the motor started came my father screaming at me I was on my mother’s side of the car (we had all the doors locked).He threaten to smash my window with his fist if I didn’t open the door. Now he and my mother started yelling at each other than his fist went throw the driver’s side window.

We all screamed in terror as the window broke into a million pieces. I remember my father stumbling away from the car into the house blood dripping everywhere. Then in our horror our mother gets out of the car and follows him into the house to see if he was ok. Well needless to say 4 children were deathly afraid that their mother was in the house getting killed, this fight was one example of many violent battles. When you are young you almost see your parents as immortal and the idea that one could turn on the other was just too much to handle. We were kids we couldn’t really fight back not like today child abuse really has come along way in 30 years. What I find strange to this day even in the early days I had a little spirit inside of me that could reason and look out for myself I knew something was wrong with him he just wasn’t right.

You might ask yourself what does this have to do with breast cancer? It took me allot of years to understand that even bad can prepare you In life for worst trails .You might think to yourself how much worst can it get than having cancer more than once and a not very good childhood. Well the good news is that my father took of for parts unknown when I was 12. I went to high school and some college and married a great guy. I worked in a factory and retail management for allots of years before my cancer. I was restless never seemed to settle down really we bought a house raised Siberian huskies we choose not to have children. The eighties and nineties were expensive times to live it took every bit of our money to keep our modest home going. We always knew that we loved each other (still do) we worked hard and it seemed to be never enough.

So many broken children grow up to be broken adults they go through their lives never understanding why they do the things that they do. So many of us can’t figure out why things happen too us and why can’t we can’t just enjoy life. For some of us it takes unbelievable changes to wake us! Cancer certainly can do that, it wakes you and shakes you and throws you against the wall. God certainly comes into play here let face it folks chemo is not really a cure but it is the best we have for now. Praying sure does help I had people of all faiths praying for me I figured that everything helps. I had so many warm wishes and kind words it did kind of surprise me. Personally I wasn’t the type of hugging emotional person that alot of people are if you knew me you knew. I was a very good friend.

I wasn’t fake just a bit reserved but kind and good to all. Cancer did change my personality some I would do the things I would never normally do. One funny story was I was doing an art show (yes folks I found My art again) that’s what I went to school for. Now the a woman in the booth near us was walking around this is common in art shows before the customers come in allot of vendors network with others find out about shows etc. Our new friend seemed really upset and than she blurred out to me that she didn’t know why but she just felt she had to tell me about her possible breast cancer diagnose. She was waiting for biopsy results now whether it was divine or not I couldn’t really know for sure. I told her my story of more than one cancer and having stage three cancer and being a survivor at the time of 5 years. We talked I think she felt a little better I gave her a hug and my phone number and told her to call me if she wasn’t ok but and happily she never called me so I am guessing she was ok.

But just chance meetings like that with people now seem to fill my life. I would never have done than before cancer did I care about for people yes more than most but I never would have given of myself so easily. When for a lot of years of your life you emotions are going all over the place you never trust them and you kind of don’t feel the way you should when things happen, this will be true when the cancer rx comes.Now remembering the beginnings of my treatment what could I say about the day? When I was told it was a sad day and believe it or not folks I was told over the phone and than it was the call to the family surgeon. Now what can I say about this man he is a wonderful person I knew him since I was 12 it couldn’t have been easy for him he knew my whole family and my mother worked for friends of his. Now stage 3 cancer is not a good Rx when your surgeon comes to sit on your hospital bed you say to yourself Boy am I in trouble! It seemed so unreal like one of those sad movies on Lifetime TV where the woman is brave and everyone cries. I wasn’t that noble I was mad! He wasn’t going to tell me I was going die!

I want to talk little about stem cell transplants the science was supposedly there that this was a good thing for people to do with not good outcomes. A lot of the doctors don’t tell you that you have a high percentage of not making it through the transplant (this is dangerous stuff). Kind of you have to risk your life so you don’t die of cancer later. Either way you could die talk about your no win situation, what a decision to make. Alot of times I held my breath like a swimmer would jumping off a diving board and take the plunge. Well after 16 days in the hospital and 3 pints of blood later I went home to recover, gain strength and get radiation (and of course go bald again after the stem cell), chemo for 7 days does make you lose your hair again. I certainly understand why men don’t like to get bald. But for men it is sexy, for us women our heads look newborns all grown up. Yes, Wigs are available but have you ever really tried on a wig? I still think wigs are for certain people not all. Trendy gals who love to change their look and don’t have to draw on eyebrows and lashes and have a pale look to there skin no matter how much makeup.

Radiation was an interesting thing to go through you kind of went so is this it? After all the treatments from chemo to surgery this treatment kind of fools you the burns came after about a month and hurt till I was done of course they give you cream but that was about the only thing they did for it. It was more time consuming more than anything was. Meetings with social workers took on an interesting twist Have you ever been told you were too strong? Till this day I never understood that ! My husband had the good sense to look at this person and ask what do you want her to do? Sit in the bed and cry all day? So please know that everyone is different none should tell you how you should feel. What could I do I had so much to deal with besides my own illness Looking back God had to be watching out for me that all I can say about it, if not I think the stress alone would have done most people in.

Other family were also fighting cancer I called them and myself the circle of three. My husband and myself have been in more hospitals in the tri-state area than most. Need to know where a lab is? Is we it a good chance we knew .At least during those years other members of my family could find the right medical offices if they needed to. I became a huge warehouse of cancer knowledge. Between me and the other two members of the circle of three we had 4 different types of cancer not including another 2 family members that would get cancer later. All together I could tell you lot about 6 different types of cancer. All this knowledge was really something I could do without

The emotions of the next couple of years seeing the end for extended family members on my husband’s side was another kind of personal hell that seemed to come my way. When you understand how they feel and you know the end is coming for them and by grace of God that could be you. How are you suppose to feel? I wished so many times for remission for them both prayed made bargains with God to no avail. I could see in their faces they hung on my every word I understood their pain their fight to stay alive. If I told them it was ok it would be ok. A lot times I would lie folks not to be cruel but to give them hope. Then other members of my extended family would get some form of cancer in coming years. I found myself not only dealing with my own cancer but some many others each with different feelings and side effects of their own.

My circle of 3 is now just me, the other two members fought so hard they would want me to go on and live a good life they know where ever they are they weren’t forgotten they have a place in my heart like so many that pass from us. They would want their story to be known they are your fathers your mother’s sisters and brothers average people who lived a quiet, life, good people, who worked hard but left the world to soon for us all.

Life does go on I look back on all the things that happened some good and not so good and wonder what has come from it all. As most spiritual people would tell you God doesn’t give us nothing we can’t handle. Well folks I have had my share and half the town’s share. Writing this almost 8 years later I can recall how I knew the very first day that I was going to fight this off. I have been somewhat successful though I did have a problem with uterine Cancer but I had a good outcome with that too. So many of us get the news you have cancer and we have the choice to fight it off the best we can.

I always thought of my Cancer as liking to the Civil War. Brother again brother so to speak your body fighting off the great evil cells that turned on the good cells. I remember once talking with an artist friend who ask me once this question“ What would I paint on a cast of my body? (She did sculpture) My answer was the battle of Gettysburg because a great emotional and physical battle was fought there. The battle was the turning of the war for the north and the end of a horrible time in history where Americans fought against each other. . I do pray for my own tide in my war, my tide is do, the little spirit in me needs to go on vacation she has been through allot. Well as I end this piece I limp into the sunset bruised, scarred but beaten never beaten just wiser bout life.

Shelley's Story

My story began October of 1999 as I was breast feeding my 9 month old son. The lump around the end of my nipple just didn't feel like the normal clogged milk duct; however I still didn't get to uptight about it. I took my son in for his 9 month check up and just asked the doctor to check it out while I was there. He felt it and felt confident that it too was a clogged milk duck and that I shouldn't worry. I will forever be grateful to him for acting on the side of caution as he said since you are here lets do a needle aspiration. I agreed and he assured me that if he could guess 999 possibilites, cancer would be the 1000 posibility. The needle aspiration drew no fluid, but again he assured me all would be fine, but again acting on the side of caution sent me down to have a biopsy. The next day I was hit with the life changing news that I had breast cancer. I felt like I had just been hit with a ton of bricks. I was the epitimy of health. I had no history of breast cancer in my family. I was 36 years old. I was a farm girl/teacher who worked hard on the farm, exercised daily, cooked all my meals from scratch, and had a strong belief in God. How could this happen to me? The rest happened all very quickly. I was sent to the best oncology doctor in the state and together we devised a plan. I agreed to do a study where I would take 4 rounds of chemo, have a total masectamy, and follow up with another 4 rounds of chemo. Following my chemo, I would have 36 radiation treatments. My oncologist told me that he would have to make me really really sick to make me really really better. I put my trust in him and my faith in God and set off on this unplanned journey. I feel I have truely been brushed with death, and have come out a winner. This journey has definately changed my life. I was determined from the get go, that I was a fighter, and I was going to win this battle. I quickly put aside the tears, "why me," and anger, and turned it around and said "why not me." I am going to win this battle and be a witness to others. I was teaching high school and coaching basketball, and chose to keep it up. I missed about 5 days of school during my enitre time of treatment. I had 3 children, a wonderful husband, and a supporting family, that never lets obsticles get in our way. I have been taught to fight them head on. There were days I felt horrible, but I would make myself get up and go to work, I didn't want to lay around and feel miserable. I learned real quickly how powerful your mind is. By going to work and coaching and being around kids, my days of yuck, were less because I choose to fight those days head on. I am not one to lie around thinking about how bad I feel. During my treatments I would sit in the waiting room; the youngest in the room, and people would marvel at my determination and my spirit. I volunteered counseling to others and found it as a great form of healing. The cancer center even had me make a DVD of my testamony that they show to all newly diagnoised patients to deliver hope to them. It is amazing the people I have met that recognize me from the DVD and say "your that girl on the cancer DVD." I surrounded myself with poitive people, positive thoughts, and never doubted that I wasn't going to win this battle. After I lost my hair, I continued to play pick-up basketball games with my players choosing to wear a stocking hat. My wig was saved for all other times; I did have to watch out for the Kansas winds as it made for a bad hair day when it would pratically blow off my head. My kids have learned what philanthropy is and means. They too have been so positive and supportive. As a family they all join me in "The Race For the Cure, The East-West Run, and The Race for Life. The have a deeper understanding of what it means to reach out to others. My daughters are members of Friendship Club; a club that has all special need students as they enjoy helping others and are not afraid to help that less fortunate child. I have learned that YOU have the choice to either fight the fight or give into the fight. You can either have your glass half full or half empty. I have always been a competitor, but I am even a strong one today. I was asked to be the captain of the Victory In The Valley East-West run and got over 200 kids from my high school to come out and support the run. It was the greatest feeling ever having all those cheering kids encouraging you as you come across the finish line. I still continue to work out and run daily and have made it my personal witness plan to always wear my pink "I am a survivor" t-shirt. Every day I have it on. It is a reminder to me as to where I have come from and how fortunate and thankful that I am every day. It also sends a message to all I meet and see that there are winners from people who have been diagnosed with cancer and you too can overcome the odds. It stops many people and brings great conversation from alot of people. I am also a walking testamony to my students as I preach to them the importance of monthly self examinations. Cancer is not the end of your lifes journey. I looked at it as a detour; an unexpected road that is less traveled. However my mission to others is for them to see the road they are traveling is paved and has been traveled unfortunatley by many, and they too have won the fight and are moving on down the road. I believe God had a plan for me to be this witness to others and this is the way he had to get through to me. I would tell others that cancer can't take away my desire to live, my faith, my spirit, my determination, my family, but it can make me a stronger person, a witness to others and a strong believer that good things happen for a reason. I am happy to report that I am 7 1/2 years cancer free and have had no reaccurance. I am on a new study and have 2 1/2 years left of taking Femara. I like knowing that I a helping fight the fight for others so that they don't have to go down the road I traveled. I still have the pair of ruby shoes that a friend sent me reminding me of the magic that not only will I live, I will thrive.

Teri's Story

I was diagnosed with breast cancer on November 30, 2006 at the age of 37. I was totally shocked as I was relatively young, very fit and healthy and didn’t fit the profile of any of the typical breast cancer risk factors. I had found a lump in my left breast in September, but I was nursing my sixth baby and didn’t think too much about it. Nursing makes things lumpy. By mid October the same lump was still there and my husband and I decided that I had better get it checked out. The first available appointment was on November 3. That began the chain of appointments and tests that led to my diagnosis. I had a biopsy on November 22nd just before Thanksgiving. Since it was a long holiday weekend I wasn’t able to get the results for several days. I started to get the feeling by the way my questions were not being answered over the phone that the news wasn’t good. I met with my doctor and he told me that I had breast cancer.

My mom had already been battling inflammatory breast cancer for 18 months when I received my diagnosis. She had already completed chemotherapy, radiation, and a mastectomy of her left breast only to discover the cancer had spread to her liver. Now we were both being treated for cancer. Having just watched her go through the process of what I would now be facing myself gave me courage as I felt I didn’t have to be so afraid of the unknown. Two of my husband’s sisters and his mother had also recently been treated for breast cancer as well. But with me being the mother of a large family of six young children, ages ranging from 17 years to 16 months, my attitude was “I don’t have time for this, I need to be taking care of my family.” Also, just the thought of possibly not being around to raise my children broke my heart. I couldn’t stand the thought of my 16-month old not remembering who her mommy was, or not being around for all of the events in their lives – the first day of school, snuggling in a chair while reading books, discovering the world, play dough, dating, picking out prom dresses and wedding dresses, staying up late into the night talking and laughing about nothing at all, watching my boys get taller than me, playing sports, driver’s licences, watching them grow into adults to see who they become – I didn’t want to miss a minute of all of the things we love to do together. I was determined to get through this. I prayed and prayed for courage and strength.

December was filled with doctor visits and many tests to determine the severity of my cancer. My amazing husband was there supporting me through each visit. We had “fun” picking out a wig together. I tried all sorts of different colors and hair styles and ended up with a nice wig similar to my hair style at the time. I was setting up a schedule for surgery when my PET scan results came back. It reveled that the cancer was “locally advanced” and had spread through the left side of my chest, into several lymph nodes, and was starting to infiltrate the pectoral muscle and a spot on my thyroid. That was a day filled with tears. The plan was changed by my doctors to start chemotherapy first in hopes of stopping the cancer from spreading further and shrinking the tumor to make it easier for the surgeon to do her job. I had a port-a-cath placed in my chest on the December 19th, and my oncologist wanted to start chemotherapy the same day. Luckily I was very sick from the anesthesia and couldn’t start my treatment that day. This allowed me to spend a wonderful Christmas with my family before starting chemotherapy.

On December 28th I had my first chemotherapy treatment. I was scared but still determined to be a good patient and try to follow all of the instructions of my doctor. Unfortunately, the chemo was just as determined as I was and I ended up very sick, but after a few days I was able to get out of bed and do my best to try and resume normal life. I found that after each treatment I would spend a couple of days being very sick, and then I would slowly recover and could resume a semi-normal life until the next treatment. The time it took to recover after each treatment grew longer (I’ll spare you the details), but I discovered that I could still be happy even though I felt totally miserable. I was able to find something to be grateful for every day.

My hair started falling out on schedule. The good news was I didn’t have to shave my legs anymore. The day after my second treatment my grandmother died. The funeral was six days later and I felt good enough to attend. Her funeral was my first attempt to wear my wig. I felt like I had a big bearskin cap on my head, but I didn’t want to go without it.

Sixteen week and eight treatments later, on April 9th, I received my last chemo treatment. Yippe! The PET scan results after chemo came back as “All identified sites of tumor have resolved. No new or residual masses are identified.” Chemotherapy had virtually wiped out the cancer! But this wasn’t the end. I still had surgery and radiation to go. I escaped with my husband for a short trip to the beach in San Diego before phase II of my treatment began.

Due to severity of my cancer I knew I would be having a mastectomy, but with my now known genetic risk factors my surgeon and oncologist both recommended a double mastectomy as a preventative measure. My husband and I decided this was the right thing to do, so we reluctantly decided to have this procedure done, and on May 22nd I had my surgery. My surgeons did an amazing job!

Recovering from surgery was very slow, painful and frustrating. I remember laying in the hospital bed after surgery and the nurse told me to press the button if I needed any thing. I couldn’t move my arms to reach the button. I needed help with everything. It took a lot of work to get function and strength back in my arms. After chemo and surgery I felt like I had been run over (several times) by a truck and left for dead. However, I gained appreciation for the fact that I would heal and be able to use my arms again. There are many people in the world who live every day with pain or permanent damage to their bodies with no hope of relief.

One month after surgery it was time to start radiation. I admit I had a grumpy attitude and wasn’t mentally or physically ready to take on any more punishment. I still couldn’t lie down or sit up easily by myself. Gratefully, I did very well with radiation, and getting on and off the table every day was good therapy for my healing body. After I was done feeling sorry for myself I was filled with determination again to get back to where I was before surgery. I kept my toddler daughter’s sippy cups on the top shelf so I would have to reach for them. I put tape marks on the wall and would try to reach higher every day.

After surgery my pre- and post-chemo tissue biopsy came back with conflicting ER and HER2 results, so my oncologist recommended that, just to be safe, I have infusions of Herceptin for the next two years. This was a big psychological setback as I thought I was just about to cross the finish line. But now, it would be back to being a pincushion. As I sit in the infusion room now receiving my Herceptin treatments I have a totally different perspective and have to hold back the tears as I watch a new cancer patient come in for his/ her first chemo treatment. Sometimes we share stories and I try to give words of encouragement and hope. I am glad that I can be an example to some of theses patients of someone who has made it through and can be living proof that there is hope, health and happiness at the other end of the tunnel.

Unfortunately, as I regained my health and strength, my mom’s health declined. The cancer that had spread to her liver was inoperable and she wasn’t responding well to medications. She died on September 16, 2007 due to liver failure caused by the spread of breast cancer to her liver. I attended one more funeral wearing my wig.S

ince completing my treatments I’ve had two more surgeries. The first was an oophorectomy to remove my ovaries as a preventative measure against ovarian cancer. This surgery was easy and I felt great after just a few days. The second surgery was to complete breast reconstruction and exchange the tissue expanders put in during my mastectomy surgery for permanent implants. This was also an easy surgery and things felt so much better after the expanders were removed. Once again my surgeons did an amazing job.

These past months I have hit several one-year anniversaries cancer free. My life has been spared and I am so grateful for each day I get to spend with my family. I can’t thank my family and friends enough for their outpouring of love and support during my treatments. They brought meals for my family, did stacks of laundry, took my car pool shifts, prayed for my recovery, sat with me during treatments, and entertained and cared for my kids so I could rest. My oldest two daughters stepped up and took care of so many things at home while my husband was at work. My friends that I played basketball every week had jerseys made with “Teri’s Team” and a cancer ribbon printed on each one to show their support while I was gone.

I can never repay those who helped me, but hopefully I can pass it on and help someone else in need. I had the example of those who sat in the infusion room with me and shared words of comfort and encouragement. I discovered that attitude is everything. You can be happy when things are down right miserable because there is always something to be grateful for. You just have to be willing to look.. Now, each day while I am exercising I think to myself “You’re not going to steal my life from me today - NOT TODAY!!! I am a survivor!!!”

Patricia's Story

My name is Patricia and I am very blessed! I am more aware than ever how important life really is to me. It was brought to my attention on April 24, 2007 when I was diagnosed with breast cancer.

What I consider a "miracle" actually happened about three weeks before, when my annual mammogram showed a tiny spot approximately 4mm X 6mm. After a second mammogram, ultrasound and biopsy, I was advised that I had infiltrating ductal carcenoma of the left breast and unclean margins. The tumor was very deep near the chest wall and I made the decision to have a modified radical mastectomy with immediate reconstruction. (To those of you who may be unaware, immediate translates to four surgeries over seven months.) The week waiting for the biopsy results had been one of the longest weeks in my life. Of course, I prayed that it wouldn't be cancer, but I mostly prayed for courage to face what was in store for me, for intuition told me to prepare for the worst. When my husband and I broke the news to our two grown children, all I could think of was that I was so glad it was me facing this callenge and not one of them. My family showed amazing strength; still I knew they worried. The next part of my miracle came when the surgeon gave me the news that my lymph nodes were clear! By finding the cancer early, it had not had a chance to spread, and going forward, tomoxifin was prescribed for five years, but no chemo or radiation! THAT is when I really first realized the importance of my regular check-ups and how fortunate I was. I wanted to run out of the hospital screaming for everyone to "hurry and get your mammograms! It can save your life!"

I decided this news was too important not to share with ohers, so I founded the non-profit group, The Dixie Connexion for Early Detection of Breast Cancer. There are 6 of us in the group including me, my daughter and four of my closest friends. Our goal is to "share the word" with the public about the importance of early detection. We also provide an area hospital and breast cancer clinic with small post-op pillows for breast cancer patients. We have done well with our fundraisers and also visit new patients in the hospital, taking them a care package with various breast cancer awareness items. This year we started the Dixie Connexion Champions survivor group which meets once a month through October. We are also participating as a team in the upcoming ACS 5K walk October 18th. The breast cancer survivors that attend our group really are Champions! They have endured all sorts of surgeries, treatements, fear and pain and sitll have a positive attitude. Their strength is contagious! I have enjoyed so much being able to share the stories of our experiences and the outpouring of support is amazing.

Since being diagnosed, I have come to realize the power of knowledge and prayer through one of the most terrifying experiences of my life. I believe that surviving has given me a second chance to "connect" with the world and my family and I am forever grateful for that chance. The roses smell a little sweeter and the sunsets more vivid. I think of it as though we survivors have a little bit of an "edge" on everyone else!

The message that I like to pass on to any of my new breast cancer friends is, "You have already found courage; take one day at a time as you move forward to finding acceptance, peace and joy in each day, and the faith and strength to "Never, Never, Never, Never give up!" Thank you for allowing me to share my story.

Sue's Story

The day Hurricane Rita hit Southeast Texas is the day time stood still. Suddenly, no one had to be anywhere, anytime soon. All appointments, scheduled events, plans became moot.

However, some of us found ourselves with a little more to deal with than just the conditions of our homes and businesses.

My home received about six inches of water, so we tore out the carpet and laminate flooring. We also cut the drywall from the floor to two feet up and tore it out. The mess was appalling. The process of filing insurance claims is demanding, and without air conditioning, telephone service or gas to drive anywhere, I most certainly felt overwhelmed.

About two weeks after the storm, I was showering. I discovered a lump in my breast. Interestingly and ironically, October is National Breast Cancer Awareness Month, and under normal conditions, I would have had no problem finding a way to get a mammogram, with or without insurance.

I didn't have insurance and since that time, many friends and even strangers have asked me how I managed to find the great care I ultimately received. This is as good an opportunity as any other to encourage people not to despair and to ponder whether or not there really is a healthcare crisis in our country.

In my case, I was employed part time at a small museum as the curator. My decision to work part time was well considered and is what prevents many people from receiving benefits like health insurance. However, I took the risk believing that as a single mother of a son with no father, I needed to be as available to him as possible. I also used my spare time to finish a degree I had started years ago. I graduated in August with a bachelor of fine arts, a month before the hurricane.

I made an appointment with East Houston Regional Hospital for a mammogram. The mammogram didn't show anything unusual, but because a lump could clearly be felt, they performed an ultrasound, which did show what appeared to be a suspicious mass. I was advised by the hospital's doctor to seek further tests. The bill totaled about $200. Very reasonable, I thought.

Next I decided to research all my options, because I was somehow sure there were some. The first thing to be determined is if I qualified for indigent health care. Hardin County Indigent Healthcare Services representative Donna Miller described their purpose."We are a state mandated, county funded healthcare program for people with little or no income," she said. "We are similar to Medicaid because we contract with local physicians and pharmacies. We do not treat minors, only adults."Eligibility is determined by the Federal Poverty Guidelines established each year.

I learned I didn't qualify for the County's assistance, so I applied for assistance directly with the University of Texas Medical Branch Galveston. At my level of income, they answered in a letter, I would qualify for 50 percent assistance.

I scheduled a biopsy and arrived at the appointed time. The procedure was only mildly uncomfortable, but did take several hours to complete. I was instructed to check with the U.T.M.B. Clinic in Beaumont for the results within the next two weeks. I think waiting for answers was the worst part of my experience.

I was diagnosed with breast cancer, and the bills I received for my 50 percent totaled about $1,600. A very kind representative from the American Cancer Center suggested I call M.D. Anderson Cancer Center. I did and was referred to Kaye Wade of the Patient Assistance Service for the Nelly B. Conally Breast Center at M.D.A. She said I could apply for supplemental financial assistance and would have to complete a lengthy application. The first page requires the patient to first phone Chamberlain-Edmonds, an organization that screens applicants who do not live in Harris County, where M.D. Anderson is located, to determine if they qualify for any other programs. "

As part of the process in determining the eligibility of someone requesting assistance," said Wade, "the patient's physical condition plays a large part. If their diagnosis is serious and requires immediately attention, that will certainly impact the final determination."I was notified within two weeks that I qualified for 100 percent assistance. I was greatly relieved.

My first appointment was with the breast surgeon, followed by an appointment with an oncologist. Several tests were scheduled, and M.D. Anderson nearly became a second home.I began chemotherapy at the end of November, which continued for six months. I was treated like a queen and given a private room with a television. If the appointment fell around lunch time, a little waiter would arrive to ask if I’d like lunch. I was served, and if I couldn’t finish, I’d take the rest home to my son.

I’m grateful that I didn’t suffer much during chemo. I had no nausea, mouth sores, and was only tired. My son began to make coffee for me in the mornings to make it easier for me to get up and take him to school. (He still makes me coffee.)

I lost my hair around January. The wispy strands that stubbornly remained I finally shaved off. Before leaving the bathroom with my new ‘do’, I asked my son if he was ready to see me.“No,” he said and held a pillow to his face. It really only took him about 20 minutes to get used to my new appearance, but I had a harder time than I expected. Each time I passed a mirror and caught sight of my reflection, I was startled. A dear friend suggested I prop a mirror on an easel and draw my own portrait. I did. I spent about six hours studying my image, translated it to paper, and had come to terms with being bald. I recently entered the drawing in the BAL National Exhibition and won first place. The whole world can see me at my worst, if that’s what I was, but I needed more than chemotherapy to get through the experience. I have included the image in this submission. It is titled Therapy.

Surgery was scheduled for late June. A mastectomy was my only recourse, so I opted for a bilateral. When I woke, I was surrounded by friends and family. My aunts and mother had planned to care for me after my release from the hospital. For the next two days, I dozed, only opening my eyes long enough to see one of my aunts’ heads peeking at me from the doorway.

Recovery is what it is, and with only a couple of problems to address, I was scheduled for breast reconstruction with the plastic surgeon at M.D. Anderson.

Today I'm cancer free, still taking my medications, and nearly finished with reconstruction. I return to M.D. Anderson for regular checkups. I can only estimate my out of pocket expenses throughout my adventure, but I'm quite sure that I got my money's worth.

Facing my own mortality was cathartic. I’ve returned to living a normal life with a newly developed sense of appreciation for family, friends and people in general. Not much gives me greater pleasure than to comfort another victim of breast cancer.

Thursday, July 31, 2008

Eva's Story

“The greater difficulty, the more glory in surmounting.”
~ Epicurus, Greek philosopher, BC 341-270

When I was growing up as a young girl I never knew anyone having cancer. I did not know anything about the disease. I only knew that people died from cancer. Little did I know that one day I would also have to face this dreadful disease, Cancer. My doctors are baffled, bewildered, and incredulous from the many cancers that I have had and survived in my lifetime. I am a true cancer survivor.

When I was a twenty-three year old young woman I found a lump in my breast. Fearfully, I quickly went to my doctor and received my original breast cancer diagnosis and had the lump removed. The Dr. told me that everything was fine however, two weeks later I came back for my follow-up check-up and the Dr. explained different, ‘news,’ that all the reports were not in from the labs and indeed there was more cancer. Leaving the office, I was devastated and crying, I drove home in a state of shock and was fortunate enough even that I made it home in that frame of mind.

Telling my parents was heart-breaking: it was horrendous news to deliver and they were so paralyzed they could not speak. My parents were immigrants and did not speak English, immediately they called the priest of our church, who introduced me to Dr. Charles McMahon, a surgeon. After seeing the surgeon, he verified my lab reports and mysteriously could not locate any. Therefore, to make sure, he had new labs done revealing that I needed to have another surgery to remove a wedge from the same place as before, so back to the hospital for another surgery. He had good news though, no cancer. We were all elated; my mother had a delicious dinner prepared along with the loving company of her sister and her family. We were a very close-knit family: with my aunt and her family. Little did we know that my beloved aunt would perish from breast cancer later in life at the age of fifty-four years.

After my aunt was diagnosed with breast cancer, my dearly loved mother had herself checked as a precaution and unfortunately she also had breast cancer. Luckily, it was removed very early and she did not need any treatments and lived to be almost eighty-one years old. Knowing the above, I was having yearly check-ups and mammograms.

In 1970, I was married to a wonderful man and we have been married for thirty-seven years. We had two great children and now are proud grandparents of four beautiful grandchildren, we were truly enjoying our normal family life.

In 1985 my husband had a heart attack at the age of forty-one. He underwent five bypass surgeries, and post surgeries, continued to have annual check-ups. In 1987, I went in for a mammogram and found that I had cancer in my other breast. A lumpectomy was necessary as it was cancer. After surgery, the Dr. recommended radiation and medications to treat cancer. I thought that was it and I continued working, raising our children, taking care of my husband, my usual activities, etc.

In 1994, during my annual mammogram another lump on my right breast was found: I was crushed, ‘Oh no, not again,’ I sobbed. Tests and procedures ensued and at this point it was standard operating procedure: I had an ultrasound, needle biopsy. I will never forget the specific Dr. who conducted that needle biopsy: he was the worst (quite possibly I was his first patient ever) and I was not encouraged just laying flat on a table with my breast hanging down the small hole: he poked and prodded so many times I screamed in agony. He got me up off the table and wrapped me in a robe and drove me a couple of blocks for another ultrasound and I was horrified yet again at the experience and the results. Trembling, sweating, tears streaming down my face: what heinous treatment and I never went to see that Dr. again. Looking back, I should have reported the Dr., but I was more concerned with my health and removing the cancerous lump. The treatments, radiation, etc. followed and after those I thought I was in the free and clear and continued my normal life.

In 2000, yet again on my annual mammogram I saw the Dr.’s face, by now the expression was a tragically familiar one, it was cancer. The Dr. sternly said, ‘I don’t like what I see,’ we need to do an ultrasound and a needle biopsy as it was certainly cancerous. This time I had to make a big decision: all of my Dr.’s sat me down and put in plain words, ‘You have no other option but to have a double mastectomy.’ The walls came crashing down and I was crying from fear of the cancer, the big surgery and was scared of the way my chest would look post surgery: my breasts, my womanhood. Questions arose: how was I going to face such a big surgery, such a life altering operation? The Dr.’s assured me that this was the best thing to do. I recognized that this was the right thing to do in order to save my life. I had so much to live for: my children, grandchildren and husband to nurture and as well as elderly parents. After consulting with many specialists, going in for second and third opinions, changing Dr.’s and medications, I finally made my decision. I have done it all yet not without the support of my family and friends. My parents supported me in their own way: as religious people, after my father’s stroke he would sit at the end of the couch listening to his favorite folk music and reading prayer books for me daily.

After my mastectomy, I had a very difficult time with the strapping around my chest, it was tedious for me dealing with the loss of my breasts and how this altered my role as a woman and as well as dealing with my numerous bouts of cancer. The Dr.’s found three cancers on one breast and one on the other, I gasped, ‘four, oh my God, was I going to make it? I had to have chemotherapy, radiation, heavy medications. After I had my extenders inserted I kept having problems in my right breast, i.e. staph infections and had to have my extenders removed three times. In addition, my treatment included antibiotics and I still need to go through reconstruction in my right breast.

Also, I just wasn’t doing well at all, this is when my oncologist Dr. Goodman recommended that I take a medication to make me feel better, and suggested Prozac. I had heard that Prozac can make you do many strange things and told Dr. Goodman this and that I may come down to his office and do crazy things which he laughed at and said, ‘I’ll take my chances.’ He assured me as always that it was going to be o.k. Going through chemo was the worst, the thorniest thing I had to do. More than my surgeries and radiation, the chemo annihilated me... I just needed to rest a lot.

In the meantime, I was off of work for quite while yet wanted to return, to which Dr. Goodman replied that I must be crazy. Evidently, crazy and stubborn, I returned to work with no breaks so that I could go home early and sleep. I had a flexible time schedule, which was helpful. I worked for a medical insurance company and did not wish to loose my benefits. Staying occupied was a priority in maintaining my sanity. I never wanted to feel sorry for myself and plenty of people including my coworkers were not aware of my, ‘situation,’ as I was very private. There was an intense amount of, ‘fear’ from the cancers: loosing my hair, constantly being sick, taking showers and witnessing my hair go down the drain, being so fragile and weak, I despised my condition and it was a dark time. I longed to be by myself with the door closed and the drapes drawn, no noises. Simply quiet.

After using all of my sick leave, my coworkers selflessly gifted me with theirs. One day at work, I was wearing a wig and was using the rest room and a coworker looked at me and said, ‘oh you look sick,’ I gazed at her and said, ‘I am very sick.’ The sympathy welled up in her eyes and she gave me a big hug, after that we became good friends and she would bring me flowers once a week placing them on my desk before I arrived at work. What a lovely gesture and a good person.

Despite the support, I continued to feel depressed; I was not responsive to any medications! I knew that my attitude had to change: by accentuating the positive and changing my perception of what my life had become: I began to feel my life turn around. Additionally, with the assistance of a counselor and many sessions with Leah de Roulet, MSW, I was helped with learning how to cope and we continue to be friends to this day.

After the surgery I developed lymphodema in my right arm which was perpetually swollen and continues to be which makes everything difficult and uncomfortable. After a year of physical therapy I am still wearing a, ‘sleeve,’ at all times, it is not convenient being that I am right-handed, yet I try to do my best.

Most of the time during my reoccurrences and recouping from them, I wore a wig, scarf and many hats. I remember after church one morning my little niece said, ‘Aunt Eva I saw your hair move. How did you do that? I replied, ‘I can only do that, it’s magic.’ I continue to do my daily activities and thought that I was done.

This time the Dr.’s found a lump in my throat: thyroid cancer. I had to be hospitalized to have the nuclear medicine treatment: surgery came first (leaving me unable to talk) and then I had to drink the nuclear liquid medication. I had to be isolated, no one could be in the room, everything was covered with plastic saran wrap, even the telephone, etc. After coming home, I had to continue in isolation for a week; not sharing anything with the rest of the family, again, the depression set in, the isolation, as I could not be close with anyone (no touching, no hugs). I was in pain and also felt that I had put my family through so much already: my entire medical issues all over again. They always put my mind at ease though, tenderly saying, ‘that it was o.k. with them and that they still loved me and nothing else mattered.’

In 2002, I was chronically exhausted; I saw my doctor and after lab tests, an ultra sound, cat scans, MRI’s, they said something looked, ‘suspicious,’ and required surgery. This time it was necessary that I have a complete hysterectomy due to my breast cancers. Again, like a broken record, the doctors performed another surgery, this time it was endometriosis cancer. When I awoke from surgery I knew that it was cancer again and I would have to endure strong chemo and radiation. When the girls saw me at the radiation oncology department, they could not believe it, that it was, ‘me again.’ Radiation I could handle but chemo was tough! Chemo was the big one…After eventually feeling better, Dr. Goodman suggested since I have kids to go to the University of Washington and get gene testing done. Thank God for that test as it saved my daughter’s life.

She became pregnant with her first child and soon after the Dr. found a lump in her breast (a mother’s worst nightmare) to see her daughter have cancer especially after just giving birth to a child. I said I would rather have it be me having cancer again than my daughter. This was a trying and painful time of my life. We were in California where they reside off and on for about one year taking care of her and her gorgeous baby boy, who we called, ‘The Miracle Baby.’

My many reoccurrences and experiences with different forms of cancer showed me that it is not easy to write about, to recall the many sad memories. I am a survivor after so many bouts with cancers and would like to help others with my story. I have learned from these experiences: I am a stronger Individual, Mother, Wife, Daughter and Friend and strongly believe that there is someone very special watching over all of us. I am a strong believer in God, I pray each morning and thank Him for all the blessings he has given me.

Currently, I keep myself busy and occupied with my family, favorite people, my children and grandchildren, with reading, going to coffee, lunch, shopping with my best friend, digging in my garden. Also, with my friend’s assistance, we research on the internet about cancer and the latest treatments. I would suggest doing your, ‘homework,’ if you are diagnosed as well as researching your Dr.’s to find someone you are comfortable with (a good fit) and who inspires confidence.

To the women and families facing the disease today, the lessons I have learned going through breast and other cancers and if I were a national spokesperson for surviving breast cancer: One of my catch phrases which brought me through difficult times during my many cancers is, ‘This too shall Pass.’ My hope is that you think positive, is kind to yourself, family & friends, do good things in life and good things will happen to you. Learn how to love, give, forgive, always keep yourself busy whatever that may be, be happy and enjoy life.

Will I have another reoccurrence? I will have to cross that bridge when I come to it. I feel lucky and blessed to be alive even to write and share my story to help others.

What is most significant and important in my life today are: I want my daughter to stay healthy and raise her, ‘Miracle Baby,’ and I want to stay healthy and be with my children and grandchildren to help them in any way that I possibly can. Life is beautiful so enjoy it.

“You don’t develop courage by being happy in your relationships everyday. You develop it by surviving difficult times and challenging adversity.”
~ Epicurus, Greek philosopher, BC 341-270

Carol's Story

Hi, my name is Carol and I was diagnosed with breast cancer in August 2006. I wish there was a quick way to tell my story, I really tried but it isn't possible. I will try to only put in the largest details of the hardest year of my life.

I have had fibroid tumors removed three different times in the last twenty five years. Every time I got one I thought it was all over till the lumpectomy was done proving it wasn't. I always thought that if anyone ever told me I had cancer I wouln't need to worry about it because I would drop dead of a heart attack. That is not what happened. I had always been good at getting my mamograms on time every year. I had trouble with cysts also. I would allways worry. My doctor treated me like I was a hysteric and worry wort. He told me that cancer felt hard and imovable and did not hurt. A cyst hurt and wobbled when you pressed it with your fingers.

I eventually relaxed and went with this infor for the last 20 years.I took early retirement from Delta Airlines in 2002 to persue a career in art.I think the thing that made it really easy for me to get regular mamograms was that Delta had a bus come out every year and nurses did our mamograms for us on our lunch hour. When I retired this stopped and I got very busy painting.

The fall of 2004 my uncle got lung cancer. He was a heavy smoker and my mother and sister took turns taking care of him that winter.I think that is the first time I missed getting my mamo.He died that spring. The fall of 2005 my mother had to have open heart surgery so my sisters and I took turns taking care of her tell she was able to take care of herself. My father had passed away in 1998.This is the second time I forgot to get a mamogram. I found what I thought was a cyst in my left breast at this time. I didn't worry about it because I was sure it was a cyst. It wobbled, it hurt, and there was no history of breast cancer on either side of my family.My mother got well but that spring 2006 she was able to move into a better house. My sisters and our husbands spent everyday from The end of March to the end of May remodeling it to make it her little dream home.

During this time I was very tired but I chalked that up to working so hard on the house. I also didn't feel right. I couldn't put my finger on it but I had a feeling of not being well.The work finally done I had an Alaskan cruise with my husband planned for the end of June. I thought I would go to the doctor when I got back. I thought if this was another fibrous tumor I didn't want to have it removed before I left. I put it off till the middle of August.They did a mamogram then the radiologist wanted another look with an ultrasound.I laid there not worrying about anything and then he said I think this is cancer. I couln't believe my ears. I said how can you tell that.What are the chances it is versus it isn't. He said he was 95 pct sure it was. He did a needle biopsy. I just felt numb with disbelief. A single tear rolled down my cheek but I didn't cry.I had an odd sense that everything would be all right even if he was correct.

I called my mother and told her and she cried. Everyone I called cried. I'm the one who ended up consoling them.I decided right then that crying or feeling sorry for myself was not an option. I would only do and say things that were going to help me. After all what was the ulternative. I was going to need all my energy to fight this. Crying gave me a headache and sinus infection. I didn't need that on top of cancer. If something in no way helped especially if it in some way hurt it just put it away from me.

Orignally the tumour was thought to be the size of a very small pea and I would be in the early part of stage one. An MRI was done and the tumor was actually the size of a golf ball but it was thought that I was probably still technically in stage one. I had a great surgeon. He said we were going to do a new treatment that they have been having really good success in Italy.

First we would do chemo them surgery not the other way around as usual.He said that by doing chemo first they could tell if the chemo was actually working. If the chemo worked it would destroy the tumor or shrink it and then a lumpectomy could be done instead of a mastectomy. With a five year course of an estrogen blocker the chances of recurrance was only about 1 percent more with a lumpectomy over mastectomy.

His positive attitude was infectious ok I was feeling good. I went out and bought a wig that looked exactly like my hair. I knew it would be easier now than waiting till my hair was allready gone.My mother and I made plans on how she would stay with me and take care of me and go to all my appointments. My husband traveled for work at least once a week but was usually only gone one day.

Then two weeks after my diagnoses, the Saturday before Labor day my mother died of a brain hemorage. I was out to dinner with my husband when we got the call. We rushed to the hospital and were told that she was brain dead and no hope of recovery. Because it was the holiday weekend they were short staffed and had her put on a life flight helicopter to a bigger hospital. When we got there we were all told again that there was no possibility she would ever wake up. She was only living at the moment because of the life support machine. She had made a living will a couple of years before and put me down as executor. She told me under no circumstances was I to allow her to be kept on life support if it came to that. She said she gave the job to me because she thought I would be the strongest and she trusted me to do it. Was she crazy? What made her think I'm strong. I think I'm scared of everthing. A coulple of people in the family thought maybe we should give it a week or a month maybe the doctors are wrong. What if they are wrong. I signed the papers but I didn't allow them to turn off the machine till everyone had a chance to have a private goodby.She died about 20 minutes after they turned the machine off.

The following Saturday was the funeral. I was nervous because my sons fiance went into labor that morning. He was really a nervous wreck. He had to leave before the service started to go to the hospital. My friends organized a beautiful luncheon for after the funeral but my husband and I had to eat and run because we didn't want to miss our first grandbaby being born. That night Annie Leigh was born. Between grief and joy I don't think my body knew what to do. My mother wanted so bad to see that baby. She made quilts and blankets all summer. I think thats when I just went into auto pilot.

Two days later my port was put in my chest. It was outpatient surgery but the anesthisia made me very nauseous.I was sick all night. I thought how am I ever going to get through chemo. I'd rather have extreme pain than nausea. Its the one thing that really puts me away. I prayed for the strength to do what I had to do to get through this.One week later they started putting the red devil my veins.

My husband was wonderful. He insisted on going to all my treatments with me since my mother couldn't be with me.I could see it really bothered him to see the red poison going into me. A friend who went through this said it upset her really bad. She thought about how it was killing her blood cells and how poisonous it was. I decided to look at it as in this case poison was good. It was my friend it was killing the cancer. My blood cells could be delt with using Neulasta.It could all be delt with.I concentrated on doing everything they told me to do to keep the side effects down.

Ten days later I woke up in the morning and there was a clump of hair on my pillow. I touched my hair and it was coming out by the handful. My son said he wanted to shave my head when the time came so I called him to come over and do it. He suddenly chickened out. I thought I don't want to be picking up hair all over the house so I took the dog clippers and went out on the deck and buzzed it all off. I looked at the strange new me in the mirror and I surprisingly didn't think I looked that bad. I put my wig on and that was that. People who saw me that winter would say isn't it nice you didn't loose your hair.

My friends gave me soft, warm, comfy lounging pajamas and that is what I lived in. After the first treatement I could not feel the tumor any longer. The doctor couldn't believe it. A chip had to be put in so that when the surgery was done the doctor would know what area to take out.I got the sores in my mouth but managed them pretty well by doing what I was told. They never got unbearable. I didn't get the dereaded nausea either, however I got a really bad case of acid reflux which they said was a form of nausea. It really hurt and was very unpleasant but hey didn't I say I'd rather do anything even pain over nausea?

The Monday before Thanksgiving I was opening a jar and a horrible pain went up my arm. I looked down and it was purple. I went to the emergency room and they found I had a blood clot that went to my lung. I spent that week in the hospital. My luck was that I was put in a room that was right outside the life flight helicopter pad. I thought about my Mom and tried to stop the tears. I refused to die like this all alone listening to that thing land every half hour. I couldn't believe how often it was used.I didn't sleep all night so I slept all the next day.

Thanksgiving was postponed till I got home. The first one with Annie. Besides cancer another thing I'm terrified of is needles. Wouldn't you know that know because of the blood clot I have to give myself a shot in the stomach every day for two weeks. I can't stand anyone else to give me a shot I can't do this. For two days I drive 25 min each way to have a nurse give me the shot. This was a big inconvenience so I had them show me how.The funniest thing anyone has seen is the first time I had to stab myself in the stomach. I screamed, then looked up and said, oh that wasn't so bad.It was actually easier for me to do it than someone else. Needles no longer bother me.

Another lucky thing to come out of this. During this time on one of my good days I painted a pine china hutch in my kitchen white. No one could believe I had the strength to do that, but it made me happy. I felt like I bought a new piece of furniture. Just before Christmas I had my surgery. The tumor was only the size of a beebee.He got clean margines and my lymph nodes were clean. Hallelujah. The board decided that since the tumor wasn't completey gone, to be safe I need a round of a different chemo in case. My hair was about an inch long and it fell out again. This chemo wasn't quite as bad as the first but different. My finger nails and toe nails turned black, like I was recovering from them being hit with a hammer. They didn't actually fall off so no problem, nail polish and noone could tell.

I was very tired with all of this but all winter I listened everyday to beautiful music, and watched feel good movies. I couldn't do art or read because of the fuzzy brain chemo give you. Also my eyesight was effected and my glasses were no use. I was told not to get new ones for about six months after I was all through because they would get better and I didn't want to get new glasses twice.

May and I start six weeks of radiation. After all the chemo it seemed like a piece of cake. The tiredness was overwhelming and I did get blisters but I was finally done.My hair grew back. I don't think I'll ever grow it long again. I learned life if too short to be spending so much time doing my hair. There are much more important and fun things to do.

July 3 2008 was my one year mark.I'm happier than I've ever been in my life. I appreciate now all the things even the very small ones in my life so much more than I ever did. I realize what is important. My family and spending good quality time with them. The things that used to make me angry no longer do. They seem so unimportant.I look at everything differently.

One thing that happened when my radiation started that was worse to me than the whole cancer thing is, that my son and his fiancee split up. He was davastated. That was harder for me to watch than anything. But my new found positive way of looking at things has paid off there too. We have a good relationship with Annies mom. Custody was worked out to everyones satisfaction.

I'm painting again and have my old enthusiasm back. I've learned no matter how black something looks things will allways get better if you have the right attitude. I hated having cancer, it was really hard but I think it was worth the positive things I gained from it. Someone told me the other day that they thought I was the strongest person they know. They thought I could handle anything. I still don't feel like I'm strong but maybe that is what being strong is. Its not that you don't feel the pain as much as anyone else does you do. But you do what you need to do to get through it you don't buckle and cave.

Don't forget to get your mamograms. If I had gotten my mamograms when I should of it would have saved me lots and lots of agony. Getting detected early I would only have needed a lumpectomy and radiation.That would have been a piece of cake compared to all that chemo.I urge everyone who reads my story to really take this information to heart. Early detection can save your life and save you from being way sicker than you need to be. Also if you have a doctor that does not take any lump you have seriously, get another doctor. If they think it is a cyst it is an easy thing for them to aspirate it to make sure. I have a couple of friends who's doctors thought they had a cyst, tried to aspirate it and found it was not a cyst. When they did a needle biopsy which is also a relatively easy thing to do they found it was cancer. If they would have just assumed it was a cyst another year would have gone by. Another year of growth which could have meant the difference between life and death, or the difference between lumpectomy and mastectomy and radical treatment.You are just as important as everyone else. Take care of yourself so you can be around to take care of the ones you love.

Megan's Story

I was diagnosed on Tuesday February 14, 2006. I was 29 years old and a mother of two great kids. My children were 3 and half and almost one. I am a hairdresser and a nail technician. On the day that I was told I had breast cancer I had to go into work right after and do some clients. That was very hard but I have the best clients around. I got done with my clients and my husband and I went home and made a lot of phone calls and I had an appointment on Thursday with a Dr. at Huntsman Cancer Instatute. My husband and I went to the appointment and the following Friday I was having a lumpectomy and sentinel node biopsy.

I have no family history of breast cancer but because of my age I decided on having a bilateral mastectomy. I was told I had a 40 percent chance of having cancer on the other side in the next 20 years and I didn't want to have to go through it twice. I have not had a reaccurance. I had the mastectomy the following Friday and was told that I had postive lymph nodes so they wanted me to do Chemotherapy and Radiation. I started Chemo 4 weeks later, and 4 days after my daughter turned one. The hardest part so far was that I couldn't lift my daughter. There were times when I couldn't get her into her crib and she would take a nap on the floor. I did 8 treatments every two weeks. I ended up with a port in my chest because they had a hard time getting my veins. I was also going to get Herceptin for a year after chemo and that was going to be administered the same way. They say that I did great with the chemo and I would take my nausa medicine and it seemed to help. My last four treatments would knock me out for a day or two because my bones would hurt so bad that I could barely lay in bed.

I started radiation 3 weeks after I was done with chemo and did that five days a week for 5 and half weeks. I got very burned in my armpit area. One day I went in and the techs even felt bad because of how it looked. I completed that and was on to the next thing. Surgery to get the expanders out and put in my implants. I had surgery the end of April 2007 and had to go another 6 weeks of no heavy lifting. At least this time my daughter was walking. I got the port out the end of July and have just had follow up appointments since. This process has made my husband and I much closer and we learned to communicate at lot more. I also learned that it is very hard for the caregiver. My husband wanted to fix me and he couldn't. My kids were very supportive and my son was always my cheerleader telling me I will be ok.

When I was diagnosed I never thought that I would die from this but I do think that we will be affected by it again somewhere. I want my kids to be able to look back and say "My mom did it and it will be ok." I have worked off and on throughout this process and my clients have told me about how I have affected them. I have some that can't believe what I went through and that I am happy and healthy now and it makes them think their problems aren't so bad. I have friends that said they would have given up and they were amazed and how up beat and positive I was. I do think that having my family around me helped me want to beat it. I have to be there for my kids, and husband.

I am taking Tamoxifen for the next five years. It does have some side effects but it isn't as bad as cancer coming back. I'm sure that there is so much more that I could tell you about the process and what I went through. I can tell you that I am very lucky to live here in Salt Lake and to have the great doctors I have had. They have all been wonderfull and I think of them as a friend. Cancer has changed my life in many ways but I also have grown and learned how strong of a person I can be. I have experienced a lot of things in my life that has made me grow and I can chalk this up as another one.

Laurie's Story

My story starts out with the fear and drama that most of us start this journey with. I was pregnant with my second child when I first felt what is now called "the lump." I didn't get it checked out right away because I was pregnant and nearing the end of my pregnancy. I wasn't sure if it was a scary lump or just part of being pregnant and all the changes that come with it.I delivered a beautiful baby boy and decided to wait and see what happened. When he was about 2 months old I was pumping some milk after I had nursed and noticed that there was blood in my milk. I was frozen with terror. I knew this was no ordinary lump. It needed to be checked out. After meeting with my obstetrician and being referred to a surgeon the decision to remove the lump was made. I decided not to biopsy it and just wait until they had all the tissue from the lumpectomy to get the full story. On Monday November 21, 2005 the news came. It was cancer, I was 27 and completely shocked. Like everyone else who has been there the thought was what have I done wrong? Why is this happening to me? After driving home numb with the diagnosis, I allowed myself to be numb but only until the next morning. Then I was ready to fight! The mastectomy was two and a half weeks later. Chemo started a month after that. Time dragged and life was a blur of treatments, blood draws and many days counting down the moments until you knew you could make it through another treatment. Eight rounds of chemo were followed by twenty five days worth of radiation treatments. No matter what the trial there will always be setbacks. No matter what the trial there will always be blessings and miracles. I had my share of setbacks, blessings and miracles. The best being able to celebrate the birth of my third chil just eighteen months after finishing treatment. She wasn't in "the plan, " but she was worth the pain to experience the miracle. So far there has been no reoccurence. I cross my fingers and pray each day that it will stay that way. I know that if the cancer comes back I will give it all I've got to beat it again so I can raise my three children. My dreams were different before I joined the pink sorority. Now they are simple with much more substance. Cancer is a journey not a punishment. You think of who you were, who you are and FIGHT each day to become the person you've always dreamed about being.

Carletta's Story

In 1980, at age 24, after I had just had my third child, one day I noticed some leaking coming from my right breast. I subsequently went to the doctor, had a mammogram, and was told there was an over-secretion in one of the ducts in my breast. This continued on and off for about 10 years and at age 34, I went for another mammogram and was told I still had the over-secretion of that duct in my right breast. After turning 40, one morning I awoke to find blood secreting from my right breast. I went immediately to the doctor and after extensive workup, was told a polyp was found in my right breast; this was removed with no abnormal findings, but I began going every six months for a mammogram and ultrasound. Three years later, I was released only to return once a year for a checkup.

In August of 2000, one day I noticed a knot in my right upper breast. I immediately returned to my doctor, and this time I was told I did have breast cancer. The doctor said I had some important decisions to make. After much thought and prayer, and having a family history of breast cancer, I chose to have both breasts removed. Upon removal of the right breast, the cancer was found to have infiltrated out of the duct into the breast; removal of the left breast revealed abnormal cells had developed as well. I thank God for the wisdom of choosing to have both breasts removed.

This is where my true journey of faith began. I am a wife, mother of three, grandmother of eleven, and a Beautician, owning my own business. My battle with breast cancer was one that was not won alone but with my Savior, Jesus, who revealed to me that his timing is perfect, and when there are times I cannot trust his hand, I can always trust his heart. He would bring scripture to my mind to strengthen me such as his yoke is easy, and his burden is light. My husband always let me know he loved and even without breasts, made me feel beautiful. My Sister, Claudia, encouraged me to go ahead with chemotherapy instructing me that I was obligated to live until I die. My Sister, Claudette, said to me “The pain will last for a moment, but the glory will last through eternity.” A friend who had battled cancer simply stated “It is doable.” My children were there to change the dressings, empty draining tubes, and help out where needed. I know my mother spent countless hours in prayer for me. I thank God even through being exhausted, sometimes not being able to think clearly because of the chemotherapy, God gave me the strength to still work on the days I did not have treatments, I thank him that I never lost my hair, and I can say with complete honesty, I was not afraid. Just as Job said, “Though he slay me, yet will I trust in him.”

At age 52, it has been eight years now since my diagnosis, and I have had no recurrence of cancer. As I sit here remembering that time, I am truly thankful for what God has done for me. I have shared my story with so many for it has become such a great part of my life and testimony. I have had the opportunity to encourage many through my story and would not change going through cancer for the world. I have truly learned through cancer that I can do all things through Christ which strengtheneth me. As my good friend said to me, “It is doable,” and when you come through it, you have a great opportunity to encourage others, tell of your faith, and make a difference for someone else. I appreciate so much for the opportunity to share my story, and if anyone reading this now is battling breast cancer, just remember that you may have cancer, but you do not have to let cancer have you.

Cheryl's Story

One of my goals in life was to get married and have a family. After graduating from college, I met the man of my dreams and we were married less than a year later. We had been married for seven months and were just thinking of kids when the diagnosis came: I had a five cm tumor in my left breast. I was 28 years old.

After a mastectomy, I endured four rounds of chemo and eight weeks of radiation therapy. My sweet husband was there through the entire treatment. He traded sides of the bed so he wouldn't accidentally bump my surgical site. He held my hair back as I vomited into the toilet. He cut my hair short when it started to fall out, then took his razor and shaving cream and shaved it all off. (My long, naturally curley hair was one of the things that first attracted him to me.) He didn't tell me when the chemo made me smell funny. When it was over, I knew if we had survived cancer treatment, we would be together forever.

Life doesn't end with a cancer diagnosis. I have now been cancer free for five and a half years. I just gave birth to our third child, a boy who joined his 2 year old brother and 4 year old sister. I have nursed all three of my children with just one breast.

The most important thing I have learned: life goes on. After a diagnosis of cancer, the most important thing is to focus on treatment and making yourself well. Once you have been treated, move on. Don't let cancer ruin the rest of your life. There will always be reminders, but there shouldn't be limitations. A positive attitiude really is the best medicine.

Kristy's Story

I was diagnosed with Breast Cancer (triple-negative invasive ductal carcinoma, level 2) at the age of 27 and while I was 36 weeks PREGNANT with my second child.

At the time, my husband was unemployed and I was working full-time.

What's funny was that I found the lump 3 months earlier, and figured that because I was pregnant (and I had breast-fed my first child for 15 months) that I was lactating and had a clogged milk duct. I noticed it, but didn't worry about it until I realized it wasn't going away. My husband and I were having marital problems and were on the verge of divorce until I was diagnosed with cancer.

I was fortunate that I was far enough along in my pregnancy at the time of diagnosis that we decided to wait to have the baby before any surgeries or cancer treatments started. I was able to use that time to interview different surgeons and oncologists and get varied opinions on my condition and the best treatment.

In fact, the aspect that was the most unsettling for me was that I was not going to be able to breast feed my baby. I didn't worry about dying, because everyone I knew who had breast cancer (inside my family and out) were still alive.

I consulted lactation specialists and surgeons and finally found a tenured surgeon who agreed to cut into me while lactating, warning me that I might have infections from it, but he would do it.I scheduled a C section on August 4th, 2007 and my lumpectomy on August 10th, 2007.

I worked full time until I had the baby, and it was a blessing because it kept my mind off of all the "ifs" and let me focus on only the "what can I do about everything today?" question.

I had the baby and started nursing him. The first time he nursed, he had a very difficult time latching on. After a couple of days in the hospital, the pediatrician told me that he was slightly "tongue-tied" and couldn't nurse as well as other babies. It was a sign.

After 4 days of difficult nursing, I decided that I was emotionally ready to stop nursing. The hospital offered to give me free formula as long as I needed it. The hospital was such a rich experience because I would walk the halls at night, praying in my mind and thinking about the baby and the cancer and what I wanted out of life.. I also prayed to understand what I was supposed to learn from all of this.

I decided to dry up and then realized that I wanted to dry up before undergoing the lumpectomy, so I put off the lumpectomy until August 21st, 2007.

All went well, they also did an axillary dissection after finding one sentinel node with cancer.It was very difficult to pick up the newborn baby and my 2 year old son after that. I then began a dose-dense chemo regimen September 28th, 2007 for 16 weeks.

The free formula was a blessing - I was able to sleep while others fed the baby. I tried my hardest to feed him as much as I could in order to bond with him, but it was a relief to be able to let others feed him too.

There were times that I would jolt awake at night from the chemo drugs and I would go out in the living room and pray and ponder. I would feel so absolutely close to my Saviour and to my ancestors who probably had cancer too. It made me desire to research my family history and learn more about my predessors.

I went back to work on November 1st, 2007 and worked as many hours as my body would allow.In December 2007, I had to have a blood infusion because my blood counts were so low. It was interesting because I hadn't realized how much my energy dragged because I must have gotten used to it. Once I received the infusion, my energy returned and color in my cheeks returned. It was absolutely amazing.

After chemo ended on January 11, 2008, I began radiation for 5 weeks starting in March 2008.The previous problems with my marriage had been put on hold during the cancer and returned ferociously in March, and we split by April.

Cancer made me realize how much of a work ethic I had. No matter what happened to my body, I was more concerned with providing food and shelter to my children. Because I had a baby on top of cancer, I didn't have the opportunity to sit around a lot, even when I was exhausted. I chose to not use cancer (on top of pregnancy) as an excuse to be lazy. A lot of people served our family with monetary donations and meals and I was in awe as to how much support we received. I resolved that once we were on our feet that I would give more to others than I had before. Their service changed my heart and my attitude. I want to be the first one to respond when others need help, because it meant so much to me. Even the smallest gestures were absolutely appreciated. Even when people just asked me how I was doing or acknowledged that they noticed how hard I was trying.

I am so blessed to have received cancer. It has built my character and made me into so much more of a person than I was ever before. Although cancer changed me, it didn't change my husband for the best and we are undergoing a divorce. I realize that attitude during trials is so important because cancer doesn't define me, it enhanced my life and now I'm a better servant of God for it.

A few months ago, we discovered that Breast Cancer runs in my family, but never this young. It turns out that I have the BRCA1 genetic mutation and so does many of my family members. This knowledge empowers me to watch and prepare and prevent.Cancer is never the ending, it's the beginning of defining who you are as a person when times are tough.

Ginny's Story

I was sadly diagnosed with breast cancer just after I turned 24. My only child, Max had just turned 1 and the prognosis was not good. I found my lump 10 months before it was ever removed, and by then the cancer had spread to my lymph nodes. My doctors were not concerned with the lump because at the time I was breast feeding and it was thought that I had a clogged milk duct. When the lump did not go away, and I started to find more I was sent to a surgeon to have them removed. Even the surgeon did not think it could be cancer. I was just too young for breast cancer and I had no family history. Well, here I am now 30 years old, 6 years cancer free, and 2 additional babies- both girls. I am blessed. Even though fighting cancer was the hardest thing I have ever had to do, I don't regret it. My life has been changed for the better. I see the world in a new light and I look for joy daily remembering how quickly it can be taken from me. I know I am stronger, happier, and healthier than I have ever been and for that I am thankful. Breast cancer is no longer a 40 and up disease and there needs to be more awareness. Women and men need to know they are at risk and how important it is to do self exams every month, and if they do find something irregular, to be pro active and get it looked at quickly. I did not know that men were at risk until I was diagnosed. I had never even heard that it was a possibility. We need more awareness! To those who are fighting the disease now, take life one day at a time to fight, and in that day look for the joy, see the beauty around you, be grateful for the things you do have, laugh as much as you can, and surround yourself with the people you love and who love you. Before you know it your treatments will be over, the incisions will be healed, and you too will be thankful for the experience to really know what it means to live life to the fullest.

Gail's Story

Let’s start with the good news. I am cancer free as of today!

It is a relief that is for sure, but (and there is always a but with cancer) I have forgotten how to celebrate thoroughly, as in down to my core. You see I have a terrorist that lies in wait, that is ready to pounce when I least expect it. I am an eight year survivor in this war on terror and I have the scars to prove it (two reocurrences). Living with cancer is a marvelous thing – the moments of simple clarity, the aweness of awareness, the breathe of life, the hope of tomorrow, the dreams of a future. But wait, there It is again, a feeling in my gut, a sickening tug that reminds me I have stage IV metastatic breast cancer, there is no cure. I want it to go away so desperately, and I do my best to do just that by eating organic, doing yoga and tai chi, meditating, long walks at the beach and keeping stress at bay. These are things I can control, and I feel good about doing them, but I do live cautiously not carelessly. I cannot be reckless I need the health insurance.

Let’s go back to the good news. I am cancer free as of today! I live today because of smart doctors, medicine that my cancer responds to, and a good attitude - what this means I cannot tell you exactly, except that I am by nature an eternal optimist. I am also very lucky, I have a wonderful supportive husband and two beautiful daughters who have grown to be wonderful adults. I am also blessed with a strong will and perseverance. I will not take no as an answer or leave a stone unturned when I am faced with an obstacle that my life may depend on. I have earned my badge of courage but I do not wear it outwardly, as the terrorist might snatch it away.

Let’s end with the good news. I am cancer free as of today!

Thursday, July 24, 2008

Charlotte's Story

Hi, my name is Charlotte & I was first diagnosed with Breast Cancer in my right Breast in 1999 which I found myself doing self exams. I went to the Drs. & they confirmed it was Cancer, I underwent a Mysectomy & Chemo & 5yrs. of Tomixifin & was cured Yea.!!!!!!!!!!!!! & I had reconstructive surgery a year later. That Chemo was tiring & I lost my hair, but I was alive. I learned that nobody is immune to this horrible disease. I was on cloud nine because I was cured. Well, here it is 2008 & in Feb. while doing my self exam I found a lump in my left breast, I was devastated.!!!!!!!! & this was after just having a mammogram & ultra-sound in Jan. So Feb. or March not sure, I found the lump, anyway I immediately went to Dr. & yup it was Cancer, so had another Mysectomy on left Breast & started reconstructive surgery & am now on round 3 of 8 rounds of Chemo & then radiation, this was was a little wose then first one. I lost my hair about two weeks ago, am trying to be positive, but have my moments. But I'am a SURVIVOR.!!!!!!!!!!!!!!

Kim's Story

I was diagnoised 3 years ago at the age 39. 11 months after my sister died of cancer at the age of 42. She battled the diease on and off since she was 32. I thought that I was doing everything right to protect myself from being another victim. I ate right, had regular mammograms, exercised regularly, I would not take birth control pills and I even nursed my babies.

I will never forget the day that I discovered my lump. I had just drop off my daughter and I realized that the seat belt was bothering me so I rubbed the area because I did not remember hitting myself and that's when I felt the lump. I can remember getting a sick feeling in my stomach because I just knew it was cancer. I

drove home and told my husband we both cried all weekend long. We did not tell anyone. We waited until Monday after having an ultra sound that showed it needed to be removed especially knowing my family history and after my sister had just died 11 months before of breast cancer. When I told my children the first words out of my 13 year daughter's mouth was "Mom you're going to die you like Aunt Lisa did". I told her that I was going to do things differently than she had and that I was going to fight it with every thing that I had in me. I knew that I was going to have to be the strong one in family because my husband was taking it very hard and my family was still dealing with the death of my sister.

I decided to have a bilateral masetomy and to have a strong dose of chemo. When summer was over I went back to school with half of my chemo behind me. When winter got here i was ready to think about reconstruction.I then under went 3 surgeries to reconstuct my breasts. I am happy to say that God guided me through this whole ordeal. My family and I have survived and now know more than ever how precious life really is.

I am fully recovered from the cancer now I just worry about my bones because the chemo and the medicine have weakened my bones a lot because I have cracked several ribs in the last couple of months. I have tried to become an advocate to help breast cancer patients in my town because I feel that God has gotten me here for a reason. I always tell women that they need to looked at all their options and decide what route is best for them and that they need to put their feet back on the ground and take off running and not look back or have any regrets. I also they them to look ahead and set their goal to the future mine was for the Christmas holiday that year. I also tell them that they need have faith that all will be well just go through the treatments and do what you have to do to get well. I also tell everone that I talk to to make sure they do their mammograms regularly and also to do their monthly self checks but we need to know when something changes in our bodies because it can make the differnce in what type of game we will play with our recovery. Had I not been on top of my health I might have fought a whole different ball game than I had to fight. Knowing is power. So keep the faith and move forward.

Kathy's Story

One of the greatest lessons and gifts I have learned is, life is not to be taken for granted! Live each day with no regrets and enjoy the sunshine, because none of us know what our future brings.

Diagnosed with breast cancer on August 24, 2002. I under-went lumpectomy surgery on September 3rd, followed by six months of chemotherapy and three months of radiation treatments. This life changing series of events could have been devastating and often is; however, I chose not to let it!

I coach volleyball and softball at the high school level and after my diagnosis, my athletes chose to wear pink ribbons with my name to every practice and game. They were committed to wearing them until I beat the cancer. My sixth graders begged to wear my wig and watching their reaction to a bald head relieved me of ever wearing it again. Their support meant the world to me and partially because of the kids, I missed only thirteen days of school through my surgery, 6 months of chemotherapy, and seven weeks of radiation.

Instead, I vowed to do whatever I could to help in the battle against this number one cancer killer of women. In April of 2003, only eight months after my diagnosis and while still involved in chemotherapy and radiation treatments, I organized a “strike out cancer hit-a-thon” to raise money to donate to the Susan G. Komen Foundation Race for the Cure. The RHSM softball team rallied around me, as did three public schools in the state, and $12,000 was donated to the Foundation that first year. In the 2004 hit-a-thon, my efforts were to involve as many young people as possible in this endeavor, we involved students from seven public schools and were able to raise a total of $22,000 for breast cancer research. In 2005 & 2006, 20 more school softball teams joined the efforts and over $24,000 was again donated to the Komen Foundation.

My passion for this project led to the establishment of what in 2007 became known as “Swing for Life, Inc.”, a not for profit organization whose annual mission is to host fund-raising hit-a-thon events to raise money for breast cancer research, with 100% of the dollars raised donated to the Huntsman Cancer Foundation. Over 40 high school softball and baseball teams from public schools across Utah participated in 2007, raising $75,000, $10,000 of which went to the Wellness Center at the Huntsman Cancer Institute where cancer patients go to get their physical side back, the remainder donated to cancer research at Huntsman. This year’s event was just as successful, with hundreds of students from 45 public and private schools participating, all of them excited to be involved in this cause, proud to collect their pledges and submit their donations. Our grand total in the six years is $215,000 for breast cancer research!

As long as I can, I will keep building this foundation until we find a cure. Every year we enlists more and more teams and sponsors who make monetary donations directly to Swing for Life or donate merchandise or gift certificates that I then uses as door prizes to help make the hit-a-thon event even more fun for the participants. I organize student volunteers who take on a myriad of jobs that need to be completed in order for the hit-a-thon to succeed. Determined to make the opening ceremonies of the Swing for Life event special, I also involve the local media, and have even been able to enlist the help of the Jazz Bear, Bumble the Bee, and Utah Grizzlies, Grizzbee at the event!

In addition to the festivities on the day of the hit-a-thon, part of the weekend’s events includes a sleepover in our school’s gym for the softball teams, a question-answer discussion with the students regarding breast cancer and its detection and prevention, and a sharing of what the event means to each student via their shared comments. Two years ago, when I learned through these conversations that a softball player at a local high school had a mother who had recently passed away as a result of cancer, I returned the money that that team had raised during the hit-a-thon to the family of this student to help defray medical costs that had accrued as a result of her illness. It was a touching moment as the high school junior cried in my arms.

Through our efforts, this hit-a-thon concept continues to grow in strength state and nationwide, as it has spread to schools in Colorado, California and Arizona. I hooked up with Kristin Mort, current softball coach at Mesa State in Grand Junction, Colorado, this March and was the guest of honor when Mesa hosted a “Strike Out Cancer” game, all proceeds donated to the Swing for Life fund-raiser. In October, I dropped the puck at the Pink in the Rink at the Grizzlies hockey game as well as threw out the first pitch at the Salt Lake Bees 'Huntsman Breast Cancer Pink' baseball game in May 2008.

It’s been 6 years and I have been blessed with good health and have kept the cancer from coming back. No matter how big Swing for Life becomes, I will always make sure 100% of the money goes to breast cancer research, we have a board of trustees that will never take a salary. I enjoy every minute I put into this and truly believe that my life has been changed for the better because of it. I can’t say enough about the kids or Swing for Life's Co-Founder, Kendra Tomsic, they have become soul mates on a mission and learn first-hand what it means to be involved in service for the greater good of others. I compare it to the movie ‘Pay it Forward’. If everyone did something special to make it better for someone else, we would eliminate a lot of terrible things in this world! These teams compete on the field but have learned more important lessons off the field with Swing for Life; how to make a difference in the community by giving back their time and efforts in finding a cure that could effect a family member, friend, or even themselves.

My message to others that battle this ugly disease; don’t let the beast win! Most of us don’t have to, get in, detect early, and fight like a giant with the best of attitude. I think pink everyday! Nobody plans on getting this handed to them in their life but take these lemons and make “Pink Lemonade” www.swingforlife.org