undiagnosed forum????
undiagnosed forum????
How about a forum for those of us still looking for a dx? I know there are quite a few of us in here, and whether the eventual diagnossis is MS or not, a forum to discuss our journey, or to ask questions of those who've experienced similar issues could be beneficial.
Good idea? Bad idea? Comments?
Thanks,
Mike
Good idea? Bad idea? Comments?
Thanks,
Mike
Re: undiagnosed forum?
Hi Mike,
I have forwarded your suggestion to the administrators.
NHE
I have forwarded your suggestion to the administrators.
NHE
Re: undiagnosed forum????
Hi Mike,
The ThisIsMS site had a technical problem for a while that prevented the addition of a new forum. This problem has just recently been fixed! I have gone through my old emails to the site's administrator and resent him the suggestions for a couple of new discussion forums. Your suggestion for an "Undiagnosed" forum was among them! Hopefully, this will get taken care of fairly soon.
NHE
The ThisIsMS site had a technical problem for a while that prevented the addition of a new forum. This problem has just recently been fixed! I have gone through my old emails to the site's administrator and resent him the suggestions for a couple of new discussion forums. Your suggestion for an "Undiagnosed" forum was among them! Hopefully, this will get taken care of fairly soon.
NHE
Re: undiagnosed forum????
This that would be great, Im one of those who are getting closer to MS diagnosis. Also started taking .R - Alpha Lipoic Acid, Acetyl L-Carnitine and Nigella Sativa Oil.
Re: undiagnosed forum????
Thanks NHE, now that I am diagnosed this isn't as important to me, but I think it would be helpful for others.
Mike
Mike
Re: undiagnosed forum????
Hi!
I've just realized that there isnt a "Limbolanders" board, it is so important as there are loads of people on another site having a lot of the symptoms but clear MRIs, this is such a relevant issue to us all, because why is that happening????
It would be a fantastic opportunity for those that find themselves in such a distressing place, to learn about misdiagnosis such as Lupus, Lyme Disease, Hughes Syndrome, Upper Cervical care, Candida/Candidiasis and I'm sure that there is many others.
Its a great idea a great post
I've just realized that there isnt a "Limbolanders" board, it is so important as there are loads of people on another site having a lot of the symptoms but clear MRIs, this is such a relevant issue to us all, because why is that happening????
It would be a fantastic opportunity for those that find themselves in such a distressing place, to learn about misdiagnosis such as Lupus, Lyme Disease, Hughes Syndrome, Upper Cervical care, Candida/Candidiasis and I'm sure that there is many others.
Its a great idea a great post
Sometimes we need to agree to disagree
freedom of speech and adult debate is so important for us to learn
freedom of speech and adult debate is so important for us to learn
MRI Reporting...
Wish we could all share what our MRI reports read, that led to our diagnosis of MS...
combined with
What symptoms were presenting at the time that MRI 'said MS'
No neuro that read my MRI's agreed on what they saw...it was such a discouraging time... for this mom of 6...
combined with
What symptoms were presenting at the time that MRI 'said MS'
No neuro that read my MRI's agreed on what they saw...it was such a discouraging time... for this mom of 6...