We can support ongoing Smith-Kingsmore syndrome research

It took us 20 years to get the actual diagnosis for Colin… 20 years ….imagine waiting 20 years for an answer to anything let alone a diagnosis…thanks to ongoing research families will not need to wait that long to get their diagnosis, but with rare diseases the care needs to be personalized. Doctors need to know as much about SKS as possible so each child afflicted can be treated appropriately …Join me in supporting real change. Let’s support good in the world and make a difference. Help us accelerate personalized, precision treatments for people with Smith-Kingsmore syndrome.

Just a small donation will go a long way to helping me meet my goal for Smith-Kingsmore Syndrome Foundation.