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hi just found you
hi i was given the skin biopsy test for sfb which came back positive.this result explained alot to me. i first went in because over the years i have had numbness and pain in different areas mostly in my feet and legs.had the nerve conduction study which came back normal, also had emg also normal.my neuro said well lets do the skin biopsy and that came back with a positive result. i go see her on the 11 th to discuss where we go from here. this has been a very quick process so i guess i was very lucky.Ok on the funny side when my dr had me stand,close my eyes and put my arms out I WOBBLED LIKE A WEEBLE LOL like they say weebles wobble but they don't fall down. needless to say it was a big suprise to me because i never noticed. so now on we go. i do have a very high pain tolerence but my spelling is awful sorry
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Welcome to Neurotalk.
Believe me, I empathize--when I was suffering through the most acute stage of my body-wide burning peripheral small-fiber neuropathy, I went through hundreds of tests and the only thing that showed up as abnormal was the skin biopsy, indicating significant reduction in intraepidermal nerve fiber density.
You should come on over to the peripheral neuropathy section here--lots of discussion, advice, and very knowledgeable people: http://neurotalk.psychcentral.com/forum20.html |
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Here is the B12 thread with medical links: http://neurotalk.psychcentral.com/thread85103.html Don't assume all doctors know this information, because many don't. |
Welcome..Hugs! :hug:
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Hello bgt
Weebles wabble but they don't fall down, love it....Don't worry about spelling I am not so good either. This site will help you to stay upright, so I want to welcome you to Neruo talk. It is good hear you still have a funny side to you. sometimes with these conditions it is hard to smile at all. I hope you can find some pain control. There are alot of folks here who have that condition too. I have cervical issues, and found NT about two years ago. I just never left, I gained alot information, and lots of new friends. Again Welcome Mr. or Ms Weeble, you can waddle in here anytime. ginnie
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weeble
thank you i try to stay positive and do pretty well most of the time.Oh btw it woudd be ms weeble lol. i have also had rls since i was a teenager (many years ago) lol in my case it seems to run in the family as with the sfn i have good days and not so good days. ialso found out that bells palsey was a pn did not know that had it twice lol. i guess over all i am lucky. oh btw some years back my dr put me on b12. sorry to run on. i will be back often
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Hi Ms bgt weeble
Glad you will be sticking around NT, Bells Pasly might have a forum for that too. I am here to talk to any time. I am 60 and stayed at NT as I have found so much help, information and hope. ginnie
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bgt1121,
:Wave-Hello:Hello and welcome to NeuroTalk. Happy to see you have come to be with us. There are great number and caring fellow members here, you will see we are supportive and relaxing place. Just let us know if we can be of any help. Our shoulders are here for support in many ways, have fun roaming around. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray: Darlene :hug: |
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i have been on 1000mcg of b12 for some time and my numbers were 556 us units so i don't know what to think.thank you for all your info have a dr appt on the 11 will know more then |
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If your answers are yes, methyl, yes ... Then I would try 5mg of the methyl daily and retest in 3 months. Some people cannot activate cyano form well, and hence it doesn't work as well for those people. If you are getting injections once a month, then, you need to bump up higher with aggressive oral as well. Positive Romberg's sign also is indicative of other damage to the brain. The low B12 is just the most common cause. |
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