Once again, I am so thankful to have found this group. I had no previous
knowledge of myelin regeneration and at last have some understanding of what
has taken place to cause the residual banding and numbness.
My story, briefly, is that in May last year I had a series of 'episodes'
over 5 days
Has anybody out there had shingles? If so, how did it affect you?
The doctor was puzzled, saying my rash looked like shingles, but the pain
description didn't sound typical. I have jolts of pain rather thanm deep,
constant pain. The rash is on my waist. I wonder if T.M. makes things
Welcome, Iris! I think you will find each one of us is different with our TM
but we all have one thing in common and that is we have found a wonderful,
caring group of new friends that help and support each other. Each of our TM
stories are different but many similar in that when it actually
Hi Betty,
I had shingles way back in the 80's. My main symptoms were pain and intense
itching. It was above my waist around the nerve pathway as the doctor said. I
was told to use Caladryl ointment to ease the itch. That was it. No other meds.
It did last a few weeks and was painful,but I
I had shingles soon after the onset of tmnot uncommonluckily
for me, the shingles were on my upper legs and bottom which were still
totally numb!!
janh
From: Betty Shaffer vasso...@gmail.com
To: tmic-list@eskimo.com
Sent: Sat, March 13, 2010
They now have shingles vaccines. I've had one already.
BobbyJim
- Original Message -
From: Jan Hargrove
To: Betty Shaffer ; tmic-list@eskimo.com
Sent: Saturday, March 13, 2010 13:20
Subject: Re: [TMIC] shingles
I had shingles soon after the onset of tmnot
I wonder about this also. What surgery would help? Does a medical person not
familiar with TM think it is an ongoing inflammation continuing to do damage?
Not sure if I have heard of headaches as a result of TM, but spasms, yes, and,
of course bladder and bowel dysfunction due to TM. The
