Is MS REALLY That Hard to Diagnose?

[Lulu54]

If you don't already subscribe to the Myelin Repair foundation blog, you don't want to miss this one - it sounds all too familiar to so many here .......  the lesson is , don't give up!

http://myelinrepair.org/blog/?p=1942

[stella213]

Thank you so much for that Lu

I'm having a really bad day and although I'm crying like a baby, I feel better.

THANK YOU ; (

Stella

[Lulu54]

I can't offer enough encouragement to everyone in limbo to read this blog.  It tells the story so succinctly.  I feel like its taken all of your medical trials and rolled them into one person's experience. - Lu

[truelove47]

I just subscribed, thank you and in clams best docs I found my neuro
listed,   That made me very happy

All the community leaders are so good

I think this site and members are great

Good whishes to all
Linda

[ack65]

Thanks for that story Lulu.  Very powerful.  Just when I am ready to throw in the towel I find something on this forum that helps me bring back my determination to figure this out. A

[Ginosmommy]

Thanks for sharing that Lulu, that was a great story!

Even though I was diagnosed fairly quickly this time around I do believe that many of my symptoms of the past year and a half were MS and no one thought twice about it being anything but "fixable with ibuprofen" or some other form of pain reliever.

[essdipity]

Yes, this is fantastic. It absolutely confirms our feelings of frustration, and our need to have the medical community do something besides conclude we are crazy.

ess