Thread: Calf cramping
View Single Post
Old 07-06-2013, 01:56 AM
mrsD's Avatar
mrsD mrsD is offline
Wisest Elder Ever
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
mrsD mrsD is offline
Wisest Elder Ever
mrsD's Avatar
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
Lightbulb

Quote:
Originally Posted by jsrail View Post
I have some cramping, but not much. I've had the Small Fiber Neuropathy diagnosis since 2008. It effects about 98% of my body surface. I do have to get up every 1-1.5 hours a night and take a few steps or I will wake up with a solid rod 3-4" in diameter running from inside my hip and down the leg, shooting out the bottom of my foot. This rod feel likes a steady 100,000 volts of electricity and there is nothing you can do but lie there and scream your head off for 45 minutes or until the Methadone takes effect in 30 minutes if you are lucky.

My SFN is idiopathic, unknown cause. I am 51 now. I have no vitamin deficiencies nor has any intake of B12, lotions. or anything works except large doses of nerve blockers and pain killers.

I find that I have some cramping due to inactivity and atrophy of the muscles. With the years of heavy meds, I am losing some muscle mass and weakening. It is difficult but since I have much pain after walking only 50 yards (and this is on the meds) I cannot exercise and therefore pay for it somewhat in cramps and muscle pain. The only form of exercise I find somewhat capable of is swimming. The water helps support me without the contact like you get walking. But this is limited by the weather and seasons.

I hope some of the suggestions here are of a help to you. All I can say is keep trying anything (except woo woo medicine) and maybe something will work. But don't be down if you don't find anything soon or at all. Just try living the best you can with the best frame of mind you can and that's good enough.

I'm off my soapbox now. :-)
This sounds very much like CMT... with the muscle wasting aspect. There are DNA tests for this, but they remain very expensive today. And so far, there are no treatments (supplement or drugs) to halt progression of this type. So pain management is all you have left.

You might benefit from reading the CMT websites, as they have drug lists to avoid (which make CMT worse), and lifestyle suggestions:
http://neurotalk.psychcentral.com/thread121564.html

Charcot Marie Tooth is not the most common form of PN. There are over 100 types of PN, and therefore many ways to help individuals with various triggers. CMT however, remains untreatable to prevent progression. Avoidance of some of the toxic drugs may help slow progression in some patients.

We had a poster here a few days ago talking about gadolinium
reactions from MRI dye...
here is a list of possible symptoms:
http://gadoliniumlawsuit-info.com/ga...emic-fibrosis/

This is the post:
http://neurotalk.psychcentral.com/post996197-33.html
you might want to talk to this poster privately.
Since you had 6 MRIs, I thought to mention this issue for
you to consider. Doctors may be obtuse and reluctant to
reveal this side effect to patients.
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei

************************************

.
Weezie looking at petunias 8.25.2017


****************************
These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.

Last edited by mrsD; 07-06-2013 at 03:50 AM.
mrsD is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Susanne C. (08-29-2013)