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Living with a leukodystrophy

need a Doctor

paulm68
  • By paulm68 · New reply September 17, 2009
  • 6 replies
  • We moved to southern Ohio, Near Huntington West Virginia. Need a Doctor who is familiar with Leukodystrophies ...

esophagus problems

paulm68
  • By paulm68 · New reply September 16, 2009
  • 3 replies
  • My son seems to be having problems with food getting stuck in his esophagus, is this part of the leukodystrophy ...

Another way to see it ...

jolocny
  • By jolocny · New reply September 16, 2009
  • 11 replies
  • I began to get a daily message from Neale Donald Walsh (:Conversations with God" author) and on this particular day I was having trouble getting a hold on my situation with ALD/AMN - it can be so different ...

white matter brain disease leukodystrophy

johnpaulangelchild
  • By johnpaulangelchild · New reply September 3, 2009
  • 22 replies
  • I am a mother of a beautiful 10 year old boy who has this form of leukodystrophy, I would like to talk to someone who knows anything about it or anyone who has it....I just joined this website....so please ...

The Five gifts of Illness by Jill Sklar

paulm68
  • By paulm68 · Posted August 24, 2009
  • 0 replies
  • Has anyone else read this and do you have any other related reads ...

losing ground

paulm68
  • By paulm68 · New reply August 24, 2009
  • 5 replies
  • this past summer my 18, Jeremiah. with Leuchodystrophy (No specific type) began to lose core muscle control. Getting out of chair is so difficult, un able to remain upright while sitting. Is there a hospital ...

Book Club anyone?

DMBM
  • By DMBM · New reply August 12, 2009
  • 2 replies
  • Happy Easter all, There wasn't quite the right topic heading for this, but it's not too far off. I was wondering if anyone would like to have a discussion thread about books/plays/movies we have found ...

Venting!

tallcrowe
  • By tallcrowe · New reply August 12, 2009
  • 3 replies
  • I hate the days when harsh reality sets in. My seven year old has 4H syndrome. It seems that every time he takes steps forward in one aspect, he steps back in others or just stops there. We don't know ...

HDLS - Adult Onset Leukodystrophy

samshdls
  • By samshdls · New reply July 22, 2009
  • 3 replies
  • I would love to communicate with anyone that has either of these diagnosis. My husband is 51 and has been diagnosed with HDLS, (Hereditary Diffuse Leukoencephalopathy with Axional sephroids) and has had ...

I'm new

hereandnow
  • By hereandnow · Posted June 21, 2009
  • 0 replies
  • Hi, I'm 39. I lost my mom to ADLD 2 years ago. My grandma 20 years ago. My younger brother (twins) have it and are 36. They are hard to understand and stumble around and are on three catheders a day ...

What is a Patient Advocate and how to find one.

samshdls
  • By samshdls · New reply May 13, 2009
  • 2 replies
  • When the management of a family memeber becomes difficult, or overwhelming, a Patient care Advocate can be a huge help. But knowing what one does and how to find one can e difficult. here are a few tips ...

The puzzel that makes up a rare disease

samshdls
  • By samshdls · New reply May 3, 2009
  • 9 replies
  • My husband was diagnosed with an extremely rare form of an adult onset Leukodystrophy called HDLS - Hereditary Diffuse Leukoencephalopathy w/ axional Spheroids. Because of it's rare nature many people ...

White matter disease

Ginger09
  • By Ginger09 · New reply April 5, 2009
  • 1 reply
  • I had an MRI done in 2006 which found 2 significant spots on the occipital lobe. Severe headaches from morning till night every day. Spent the better part of 06 in a wheelchair due to Lyrica. I just had ...

Make A Wish Design

makeawishdesign
  • By makeawishdesign · New reply January 21, 2009
  • 6 replies
  • I am an interior designer working with Make a Wish Foundation to make over a room for a 5 yr. old boy who has Leukodystrophy. Does anyone have any suggestions of things that would be helpful and comforting ...

Welcome

revdocwlk
  • By revdocwlk · New reply June 16, 2008
  • 3 replies
  • Hello! Welcome to this new section of the ULF web site. I am Bill Kintner, ULF Vice-President and a parent of a child with MLD(now deceased). With my wife, Colleen, we have been the vice-presidents of ...

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