Cage was diagnosed in 2005 with Spinal Muscular Atrophy Type 2.

 

Spinal Muscular Atrophy (SMA) is a motor neuron disease. The motor neurons affect the voluntary muscles that are used for activities such as crawling, walking, head and neck control, and swallowing. It is a relatively common "rare disorder": approximately 1 in 6000 babies born are affected, and about 1 in 40 people are genetic carriers.

SMA affects muscles throughout the body, although the proximal muscles (those closest to the trunk of one’s body - i.e. shoulders, hips, and back) are often most severely affected. Weakness in the legs is generally greater than in the arms. Sometimes feeding and swallowing can be affected. Involvement of respiratory muscles (muscles involved in breathing and coughing) can lead to an increased tendency for pneumonia and other lung problems. Sensation and the ability to feel are not affected. Intellectual activity is normal and it is often observed that patients with SMA are unusually bright and sociable. Patients are generally grouped into one of four categories, based on certain key motor function milestones.

 

However, with his growth and gaining size by the day it has become increasingly harder to carry our little guy. He is quickly outgrowing his handicapped stroller and is in need of a manual wheelchair.

 

The problem is that insurance will only pay for either a powerchair (at a cost of over $20,000) or a manual wheelchair (low end models go between $2,000 to $7,000). Cage needs both.

 

So, we are asking all our family members and friends for their support in gaining the chair that Cage needs.

 

Please click on the link below and donate any amount that you can and wish. Even if it is just a dollar, every one counts. Or simply mail us at 407 S. Boston St, Galion, Ohio 44833.

 

There is no pressure. We are just asking those that wish to help and have offered.

 

Thank you.