This is a long post but I think there is power in story and to know the situation before prayers are lifted up so here goes.
My sister’s good friend is going through a fight against a very aggressive cancer and things are not going well. Her name is Michelle Rigney. Prayers are needed for her. Her is here story:
My name is Michelle Rigney and I was born and raised in the great state of Delaware. I went to Newark High School where I graduated in 2003 as an honor student, played soccer, participated in Spanish club and Key Club, and was also very involved in the NHS choir. I was accepted at the University of Delaware, where I would be majoring in Nursing.
I was the typical college student. But all of my college fun came to a HUG HAULT in March of 2005.
I had two amazing best friends at the time..Stephanie and Christine. I can say it was because of these two girls.. and my family I am still alive. I had a mole on my right shoulder blade and the mole had been there my entire life.. but it changed. It got MUCH MUCH darker(almost black) and it got harder on top(almost like a scab). It concerned my friends and family. I told them I would have my primary doctor look at it. And that is what I did.. I had an appt. in Nov. ‘04.. and my doctor agreed the mole looked “weird” and needed to be looked at by a dermatologist. Well.. I tried to get an immediate appt right after that, but my insurance limited me. I had to wait until March 3rd, 2005 to have the mole removed. I had cancer.. sitting and growing on my back for over 4 months!!(and never even knew it!). I would have been in that appt. much sooner if my insurance covered ANY dermatologist in the state. Once again.. my luck took charge….
It wasn’t until March 15th, 2005 around 9pm(once you have cancer you NEVER EVER forget your dates!) that I found out I had Malignant Melanoma. My mother had to tell her 19 year old daughter.. “you have cancer.” Those three words have forever changed my life.
The next few weeks went completely downhill for me. I immediately called the UD and left on a medical leave from there. I had to have a surgery on April 11th, 2005 to remove the skin from around where the mole was.. and I had to have my lymphnodes removed from my right armpit to determine if the cancer had spread to any parts of my body.
Life went back to normal.. well as normal as it could be after being told at 19 I had cancer! I was told all of my lymphnodes came back NEGATIVE! And the cancer was isolated to JUST THE SKIN! The game plan after that.. was to just have CT scans and blood work done every six months. And that is what we did. I went back to UD.. and I turned 21!!!
Well… here again my luck comes into play.. I had a CT scan in the beginning of Sept, 2006.. and on Sept. 29, 2006… I was told the melanoma that was SUPPOSED TO BE ONLY SKIN CANCER… spread to both of my lungs. Who would of thought? Your skin is the largest ORGAN in your body.. why wouldn’t it be able to spread? Well, I am not sure how you view skin cancer.. but I had no idea it was this aggresive.
My life turned upside down for a second time. I was forced to leave UD for a second time.. and this time it was gonna be MUCH longer. The FDA has only approved two drugs for melanoma.. and standard chemo and radiation do NOTHING to get rid of it(this is why I still have my hair!). The two drugs are called Alpha b-Interferon.. and Interleukin-2. These drugs are biological drugs used to bump up your own immune system to attack the cancer. (instead of having 30,000 or so white blood cells.. you now have 30 million white blood cells). Well Interferon is only standard treatment for stage III melanoma… I was now a stage IV. The drug I was “lucky” enough to get was high dose Interleukin-2. I spent four long weeks in the hospital receiving this treatment…it was honestly the worst four weeks of my life. I had never felt so sick in my entire life.. It was the hardest and most courageous thing I have ever done in my life… only to find out my tumors have not shrunk, BUT have not SPREAD EITHER!!
The good news: Melanoma is an extremely hard cancer to beat… and usually kills people within 7 months. I have lived over a year with it in my body! And I am still here!
The bad news: There are no current treatments for me to do. Because there is no money out there to support the funding for research.. I am left here to wait. Wait for another drug to hurry up and be approved by the FDA to save my life.
Here is her post from today:
FRIDAY, APRIL 25, 2008 12:21 AM, CDT
Hi Everyone-
This journal entry is gonna seem much different, but I want to be totally honest with how I feel. I will never give up in my fight…. but it would be nice to get some good news here and there… it makes a lot harder to continue..
I didn’t get any good news today. I feel like I can feel my life slipping through my fingertips and there is nothing I can do about it.
I called my doctor’s nurse to find out some results. Since my next appointment is May 5th, I wanted to know before then. She pretty much told me the following:
* All the spots in my lung(the five or so that are bigger) are larger. One spot is smaller. All the rest that are covering my lungs are unchanged.
* We now have possible kidney involvement. There are spots seen now that were never there before.
* They still see the spot on my hip, the one that was radiated. And the one on my neck.
* The spot in my mediastinum has now doubled in size.- The mediastinum is a non-delineated group of structures in the thorax (chest), surrounded by loose connective tissue. It is the central compartment of the thoracic cavity. It contains the heart, the great vessels of the heart, esophagus, trachea, thymus, and lymph nodes of the central chest.
* There is some possible spot now on the bottom of my spine, down towards my butt area.
* And almost all my subq spots (tumors that grow under my skin in the fat cells) have grown.
I have been fake to you all. I am not nearly as strong as you think. I am so scared. I’m not ready to leave this world yet. I want to believe everyone when you tell me things will be okay, but I am not sure. I have tried to remain positive.. but since December I have not caught one break. Melanoma is just spreading so fast. Even thinking about giving up half my lung brings tears to my eyes, along with how I had to lose my hair… and now I am bald. I miss my hair so much. I get so upset.. more than you all could possibly know. I am not as strong as you all make me out to be. I am absolutely sick of living this lifestyle. I have been doing this since I was 19.. and now what am I known for? Cancer. Its the only thing I do all day long. Go to doc appts and go home. I wanted so much more out of this life. I hate having no control over this. This new news has just crushed me…. I have one treatment left… I am praying and crying harder than ever it works….
I feel completely knocked down.. a million times weaker that before. I pray I have enough strength to start this new treatment on May 5th.
Thank you for all the love and support. I have my brain MRI tomorrow and I should get my results on Monday.
Love,
Michelle
You can keep track of her progress here: http://www.caringbridge.org/visit/michellerigney
I know Michelle and her family and friends would appreciate the thoughts and prayers…