Mary Schultz's Fundraiser
Please support medical research on rare diseases HSP and PLS.
Please donate to SPF to help fund medical research.
I was diagnosed with HSP in 2012. A few years later, with genetic testing, my gene mutation (SPG7) was identified. It is autosomal recessive that is usually adult-onset. So…my children will probably not get HSP, but they might be carriers. Because I recently became a grandmother, the importance of a treatment or cure to my family has become critical.
Please join me in supporting real change. Let’s support good in the world and make a difference. Help us find treatments or cures for HSP and PLS. Let's fund more medical research on rare diseases HSP and PLS.
Even a small donation to SPF will go a long way