Hope 4 Caleb
Caleb continues to amaze. Caleb had a neurologist appointment on Wednesday August 17, and he continues to amaze the neurologist with the LACK of spasticity, and his CONTINUED BRAIN GROWTH, this is incredibly rare, truly unheard of for a child with his injury. He is a tremendous fighter, but we will be unable to continue his obviously beneficial therapies without help from people who willingly join our fight for Caleb. Will you join this fight? We are in need of an upgrade to our current wheelchair van. We have a 1999 which our church purchased for us, and we are truly thankful for it, but it is in need of expensive suspension repair, and it only seats 5, we have 7 in our family;-) We have located a couple of used vans in the $10,000.00 range, so if we could raise approximately $8,000.00 we could trade. We also are in need of funds for MNRI conferences. Caleb is doing well, but tends to make breakthroughs (see results above) during and after the intensive therapy of the MNRI conferences. Intensity seems to be the important part of the equation. Caleb is a terrific young fella, he continues to work without complaint, he really shows tremendous improvement when continually challenged thru the conferences. Last but not least we do use some very expensive vitamin supplements in Caleb’s diet, if you have purchased vitamins you can understand how the costs can add up. Dad is working 2 jobs, and Mom is full time with Caleb’s care, could you help? Small donations can add up to big changes for Caleb! God Bless!
Caleb, a work in progress: