So for you..do you feel lilke you need to keep pursuing the ms thing?
Sometimes i feel that since i really feel ok most of the time..that knowing i have ms will just depress me...and the treatments for it suck!!! Who wants to inject yourself with toxins.
I dont think my symptoms warrant that...my friend's mom has had ms for over 40 years....she had symptoms when she was 18...she did ok..they didnt have the treatments back then..she was never in a wheel chair. Some things came and wnet over the years...
But she managed...
I did read somewhere that alot more people have it then are reported...they say that only 400,000 in the us have it but now they think that its over a mil. because everyone seems to know someone who has it and its somewhat of an epidemic.
Where do you live> How old are you?
I am 49, so I think I am safe. Yet, when they say the ages you usually develop it, doesn't mean it is found then, right? I def. have something neurological going on, but I don't believe it is MS. My neuro exam is always abnormal one way or another.
You're right about the treatment. My friend is trying LDN. I think that is something you do on your own, not sure. You can look it up, there's a group for it. I am told it's used for many autoimmune disorders. I have some of those, but don't want to put anymore into this body right now. I am taking 11 prescriptions daily as it is. Yuck!
I follow up with my neuro and an epileptologist, but I am done seeking an answer. I now believe there isn't always an answer. When I was diag with MS my PCP said it's about time someone put it altogether. Now that I am told it's not, back to square one with the exception that I no longer stressed at finding the cause/reason.
Good luck to you, Sally. Oh, btw there is a Yahoo group for MS, they are very nice. Here is the link if you are interested:
http://health.groups.yahoo.com/group/FriendsWithMS/
If some of the above didn't make sense it is because I wrote it to a friend who thought I had MS (she has it).
The neuro said my lesions could still be a problem and my C-spine issues are part of it. I think that she still suspects MS. She says some of her patients only ever have one attack. Who knows. I just know I am much better today (this year) than I have been for years. A lot of the symptoms above don't bother me or are infrequent.
First, the ones I have been told I have or have had:
spasticity, dysarthria, clonus, myoclonus, paraethesia, vertigo, my fav -
constipation; sleep disorder (alpha intrusive sleep), autonomic nervous
system (the tachy and syncope), my other fav - epilepsy; L'hermittes but just once and it could've
been from neck or ?, neuralgia
What I believe I have:
cognitive dysfunction, I think the jerking when trying to touch neuro's
finger is intention tremor, vestibular ataxia - when my body leans so bad
can't walk w/o Tom exerting force the opposite way by hold'g my hand,
aphasia/dysphasia - but thought maybe seizure?, speech
ataxia (I blame meds), Uhtoff's symptom (increase in severity of symptoms,
geez that doesn't leave it wide, open does it? :oP ), inappropriate cold
body parts (not meaning the Raynaud's, but my leg was a disgusting
horrible cold feel'g).
Here are the maybes:
I saw the babinski but think neuro did the test wrong.
swallow'g probs off and on(again, now with just sm. stuff)
bdbdbdbdd That's all, folks. ;o)
But I haven't fallen apart yet and I consider myself very lucky that I am not a horse (or else they would've shot me). ;o)
The MRI doesn't necessarily mean MS. I have lesions and in the area that makes MS suspect and I was diag with MS. Later I was told I didn't have MS. Here's a link to the criteria to get diag with MS...and just because you have some of the symptoms, don't jump to conclusions. I have a lot of them.
http://www.mult-sclerosis.org/DiagnosticCriteria.html
Hi Jan...thanks for your input..what symptoms do you have, and since you were told you dont have it...did they tell you what you might have?