I filed my taxes yesterday, and I am committing $500 of my return as a donation to PFS Network.
I recognize that not everyone will be able to contribute, but for those that can, I’d encourage my fellow U.S. patients to do the same.
Research and awareness are the only ways to make progress toward potential treatments, and this is what the PFS Network is working toward. We need to continue to support them as much as possible.
Additional funding will only speed up research efforts, which obviously we all desperately want.
I’m committing $500 as soon as I get my return, in addition to my monthly recurring donation. At year end, I’m hoping to donate an additional $5,000 on top of that all.
I’m not rich, and I’ll have to make certain sacrifices to do this — but it’s absolutely essential to me. I hope others will also make this pledge