Jackie Wellman's Fundraiser
A day when all individuals with HSP or PLS are diagnosed, treated and cured.
Join me and help make a difference, please give today.
We are no longer accepting donations on this campaign, but there are other ways for you to support us today!
Join me in supporting real change. Let’s support good in the world and make a difference. The more research we support the quicker a cure can be discovered for Spastic Paraplegia Foundation, Inc..
Just a small donation will go a long way to helping me meet my goal for Spastic Paraplegia Foundation, Inc.
I was diagnosed with Hereditary Spastic Paraplegia when I was thirty-two....many moons ago. At that time I was walking unaided. Now I use a wheelchair all the time. Hereditary Spastic Paraplegia is a rare progressive genetic motor neuron disease. More people in my family have Hereditary Spastic Paraplegia than do not. My 29 year old son has HSP and uses a cane at times.
The Spastic Paraplegia Foundation is run by a group of dedicated volunteers. Over 85% of the funds raised go towards research. The rest of the money is used for postage, maintaining the website, etc.
To learn more about the foundation or the diseases please go to sp-foundation.org
A cure is within reach. Exciting things are happening. Please help us. I do not want my son to go through what I have gone through.
If you would like to, please join us August 21st at Raccoon River Park from 10am to 12pm. Walk the 3.1K trail or just socialize.
Thank you for your support. I truly appreciate and love you all.