Hi! My names Mara. If you’re new to our page my son Jace is autistic with global developmental delay but he also has some other struggles like mobility issues that we didn’t have an answer to until recently. He was found to have 2 rare genetic mutations. ARID1B associated with coffin siris syndrome and another called ANK2. The exact variants he has have never been documented in the world before and there’s nobody documented that has both these gene mutations together either. We are currently on a journey of stem cell therapy to hopefully help some with mobility and other coocurring issues but have decided to pursue intensive therapy as well to get the most benefits out of the cells. We plan to do a set of intensive therapy before we leave, after we come back from our stem cell therapy and then hopefully continue on as long as funds allow and progress is being seen. Thank you for reading this far and considering donating to Jace’s intensive therapy fund. We can’t wait to document his progress for you all and appreciate all the love and support.

we now have reached enough funds for the medical side of the fundraiser so any additional donations will go towards his therapies. We are continually doing intensive therapies with more upcoming as they show so many benefits for him and will be starting with ABA therapy. Thank you all for the love and support!