Love for Jack McLean
About Jack
Jack McLean is a beautiful, kind spirited and loving 7 year old boy who
has been diagnosed with Confirmed Primary Mitochondrial Disease
Complex 2 & 3, which is one of the rarest combinations of Mitochondrial
Diseases. Due to the disease, Jack suffers from many physical problems,
including a lack of muscle development and continuous nerve pain.

Every part of Jack's small body has been affected.
The smallest things that most of us take for granted
have become daily challenges for Jack. Because of
these physical challenges, Jack requires multiple daily
medications, physical, occupational, and speech
therapies, MRI's, and repetitive blood testing, muscle
biopsies, endoscopies and more on a regular basis.

The road ahead for Jack is a long one. The cost of
long term maintenance is staggering. Over his
lifetime, Jack will need to continually see a team of
specialists to monitor all of his internal organs, in
addition to his current physicians that monitor his
ongoing physical problems. There will always be
tests that need to be performed, surgeries, travel
expenses, medications, etc. that need to be paid for.

His insurance only covers a portion of what he requires, if it covers the services he
requires at all. The vitamin regimen and other prescriptions that Jack's team of
physicians have put him on exceeds hundreds of dollars every month in co-pays
alone.

These bills have become unmanageable for his family.

Jack's family is in need of your support. Please help them by showing your love and
support by sending your thoughts, prayers and donations in their time of need.


For More Information on Mitochondrial Diseases, please visit the United
Mitochondrial Disease foundation website:  http://www.umdf.org
To Help the McLean family fight Jack's battle, please consider
donating any amount by clicking the Paypal button below.



Or Payments maybe made directly to:

Solvay Bank /
The Jack McLean Fund
Attn: Patricia Binns
1537 Milton Avenue
Solvay, NY 13209