Giant Axonal Neuropathy

"Donate what you Can to cure GAN."

Melissa Hutchinson
  • Female
Share 
  • Blog Posts
  • Discussions
  • Events
  • Photos (5)
  • Photo Albums
  • Videos

Melissa Hutchinson's Friends

 

Melissa Hutchinson's Page

Latest Activity

Comment Wall (3 comments)

You need to be a member of Giant Axonal Neuropathy to add comments!

Join this Ning Network

At 10:10pm on June 12, 2009, Lori Sames said…
Hi Melissa. Lori Sames here, from Hannah's Hope Fund (Hannah's Mom). I hope you are well. How is Alan? Did Dr. Kevin Flanigan, Utah, do Alan's gene sequencing to see what type of GAN mutation he has? If so, please email me his mutation. Also, would you ask Alan's mother if it's ok if we use some of the photos you placed in this forum for a slideshow we're putting together to play at fundraisers? Please send me an email at:
lorisames@yahoo.com Take Care Melissa! We're working hard to try to have a treatment to save these precious lives. thank you, Lori Sames
At 2:32am on May 21, 2008, Azwhayn McLean said…
I have been well, school an such. i also had some of the screws removed from my foot the other week but im all good now!!!
At 9:00am on May 7, 2008, Melissa Hutchinson said…
Ashley, Melissa, and Amanda

Profile Information

About Me
Parent of GAN Child
About Me:
My nephew, Alan, has GAN. He is 8 years old.

Melissa Hutchinson's Photos

Loading…
 
 

Badge

Loading…
 

© 2009   Created by Matt Sames on Ning.   Create a Ning Network!

Badges  |  Report an Issue  |  Privacy  |  Terms of Service