Hi Everyone -
Most of you have heard from me before - and here's where I ask for more cash! In 2008 I was diagnosed with this dreadful disease and given 3-5 years. It's 11 years later and I'm still here - and feeling strong! I owe most of that to The MMRF and the opportunities they've made for myself and my doctor so we can find the drugs that work and have a selection in the event they don't.
Having said that, I am more lucky than some. This disease can be aggressive and nasty. In 2013 I had a complete stem cell replacement and met three friends going through the same process within about a month of mine. I lost the first one within the year, the second a year after that. The third I just lost a year ago. I hate this disease and wouldn't wish it on anyone but at the end of the day I have it and I'm going to fight it - and you're going to help! When I relapsed in 2018, after 5 years in full remission, the number of drugs available to me was amazing - but it's still not a cure!
If you'd like to see more of my story you can click here: bit.ly/billmmrf
To see my speech from Laugh For Life two years ago click here: bit.ly/billmmrfspeech
And now - simply click on that link to the right - make your donation and help me find a cure!
**Want to double your impact? Inquire if your company matches your charitable donations and submit your donation information through your company's portal or HR to receive a match! Forward me your confirmation email and I can get your match added to my fundraising total!**