When I was diagnosed with leukemia on February 20, 2014, I had a doctor that held my hand and looked me in the eyes and told me that she was going to fix me. From that very first moment, I was terrified but I had a sense of hope. That sense of hope has been the crux of my strength for the past 2 years. Hope that I will survive this…hope that I will get my life back…hope that I will live to have my own children. When someone is diagnosed with ALS, there’s no such hope. They are told they have most likely 2-5 years to live in which they will gradually lose their abilities to do almost everything except for think. They are told that they will no longer have the physical capability to breathe on their own, but they will have the mental capacity to know exactly what’s happening. They are then told that there’s currently only one treatment for this disease and that it will likely extend their life 2-3 months. 2-3 months, that’s it.
I want these people to be given the same hope that I was given. They deserve it. That is why I am so humbled and honored to be working for ALS TDI, an organization that is entirely focused on research to help #endALS. An organization that is working tirelessly to help give these incredible individuals the hope they so deserve.
Today is #GivingTuesday. It’s a day to remind ourselves of what this time of year is truly about– not deals on Black Friday or Cyber Monday, but giving to those we love and to those in need. I ask that today, even if just $5, you donate to ALS.NET and help us towards our goal of finding a cure for this terrible terrible disease.
Lots of love, light & gratitude,
About 23 years ago, me, my dad and my Bumpa had a special day at Fenway Park– I was lucky enough to be taken into the dugout and meet Johnny Pesky. I got an autographed bat and ball that Mo Vaughn had just practiced with. Being a NH girl, I’d like to think that was the day I fell in love with Boston and all of our sporting greatness. In two weeks, I’ll be back in the dugout. This time, waiting for my chance to take a swing at home plate on the best baseball field in the world. The amazing individuals that work at the Jimmy Fund reached out to me a few weeks ago and asked if I wanted to participate as they offer this experience to patients at DFCI. At first, I was a little hesitant because although I was quite the softball player in the 90’s, I haven’t swung a bat in many many years. But then I thought, what the heck is the matter with me? When’s the next time I’m going to have the opportunity to bat at Fenway? The answer is probably never so time to pony up and make some memories..
As cool as it is that I get to do this, what’s even cooler is that it’s all in part to raise funds for the Dana-Farber Cancer Institute. This amazing day is put on as an effort to raise money for one amazing institution; one that is obviously very near and dear to my heart.
If you can afford to make a donation, please consider doing so. This is an incredible organization, one that not only saves the lives of its own patients but conducts research that is paving the way for treatments, preventions and cures to every kind of cancer– not just in our own backyard but all over the world. By donating to the Jimmy Fund, you are putting dollars towards putting an end to this dreaded disease once and for all. I’d say that’s a pretty great thing to put your hard earned dollars towards!
Here is the link to my fundraising page: http://www.jimmyfundfantasyday.org/2015/jessicamoran
Thank you so much for your support, I appreciate it more than I can put into words.
p.s. In honor of my 21st century batting debut, I thought I’d throw it back to my younger years!