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Neurology  (Expert Forum)
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ataxia?
This forum is for questions and support regarding neurology issues such as: Alzheimer's Disease, ALS, Autism, Brain Cancer, Cerebral Palsy, Chronic Pain, Epilepsy, Fibromyalgia, Headaches, MS, Neuralgia, Neuropathy, Parkinson's Disease, RSD, Sleep Disorders, Stroke, Traumatic Brain Injury

ataxia?

by Leah, Jan 19, 2001 12:00AM
Last year I was dx with encephalitis.

It has been 11 months.

clear mri

no other test, was Rx for speech therapy.

However, continue to be dizzy, right hand is slow and clumsy.

The worst is my speech when tired. It is slurred and garbled, with much difficulty choosing the right words for objects, etc.

Recently it became apparent that I am having episodes of not recongonising certain words meanings when spoken to me and not remembering how to spell simple words,memory now is pretty bad.

My symptoms seem similiar to Cerebellar ataxia or like that of Progressive aphasia.

My question: isn't there some test to determine what's going on?I am 'only' 40, no drugs or drinking. Very active

I go back to neuro soon

Thank you for your time.

by CCF Neuro[P] MD, RPS, Jan 19, 2001 12:00AM
Dear Leah:



I am sorry to hear about your symptoms.  I would think that some of your symptoms might be coming from the encephalitis that you had 11 months ago.  What was the infectious agent?  Did you have any seizures with your encephalitis?  I think I would start with some basic labs and do an EEG.  I might also repeat the MRI with special cuts for epilepsy.  Some of your symptoms getting worse when your fatigued is likely related to the encephalitis as your reserve is likely lower for that function.  As you get tired, the lack of reserve accentuates the speech problem.  The most likely explanation is that what your experiencing is from your encephalitis, but some thought needs to be given to other things.  So, the basic lab work such as a B12, folate level, etc.

I hope that I have helped somewhat.



Sincerely



CCF Neuro MD
Member Comments (4)

by Kay, Jan 21, 2001 12:00AM
i know this is against the rules but i cannot seem to get online

to post a question.  I have been trying for 3 weeks.  I can only get online in the evenings and weekends and it always says--no more questions.

if anyone can tell me about the frustrations of being without a diagnosis please respond.

as of now i have been told --peripheral neuropathy--

funny thing is i stepped out of bed in August--after having been out playing at the lake and hiking around and all--

well i got up and my legs were so numb and weak i had to use crutches to get to the doctor.  

he did MRI of everything --neck, cervical spine, pelvis, leg and also CAT scans and nerve studies.... it sounds like MS but no

one will say what is wrong...

each day i watch my legs get more dead, cold, and creeping up my legs

each day i feel the fatigue

each day i forget half of what i did or said

AND

each day my 15 year old gets more scared

as for me-----i am so numb i am afraid to really get mad or cry or whatever---cuz i might never stop.

so i look here for answers and

wait for the time when i will have my spinal tap --on march 5th

grrrrrrrr

sorry to ramble

kay

by To Gary from Lisa, Jan 23, 2001 12:00AM
Dear Kay,

I know.

Give yourself a break. I am learning the medical science is sort of like auto mechanic dx. They look under  our hood, run some test, rule out some stuff, scratch their head, research some more, then if all else fails, they have no other choice then do a 'wait & see' what happens next.  



Hang in there. You are not alone in that, our bodies betray us. We hang most everything on well funtioning systems. I hope you find some answers, but try not to let the journey make you lose hope.



Postings are taken PST @ about 6am.

by Rae, Jan 24, 2001 12:00AM
You may want to check out Lyme Disease. Only half the people that get it have the rash, and it is in 49 states, out there by the lake you were you were running around.



There is a huge list of symptoms including the usual arthritic ones and numbness, but also memory loss, stuttering, and lots more neuro ones. You need to do your own reading because most doctors do not understand the symptoms and want to rely on tests which are only about 40% accurate.



Go to http://www.LymeNet.org/ and read the whole site. It may be what you are looking for.

Good luck, both of you.
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