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Member Neuropathy Journey Stories: What's Yours?

Neuropathy | Last Active: Oct 17 5:52am | Replies (571)

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@artscaping

Good evening @laura163, and welcome to Connect. It doesn't look like I have to remind you that we need more information about the symptoms your body seems to be dealing with right now. You indicate that you haven't had a skin punch biopsy anywhere on your body.....ankles, hips, or other areas. This is a special test that measures the number of nerve cells you have in the nerve fibers. For example, my was .09%. That indicates that I don't have enough of those tiny fibers to be able to receive appropriate messages from my brain. So....my brain sends pain signals.

As I perused your symptoms I found many to be exactly like mine. My SFN actually showed its character early in my arms, hands, and skull. The skull area can really get riled up at times with pain as well as tingle-tangles. (my terms for the numbness and nerve pain). My feet started with a few twinkle toes and quite quickly, or so it seemed, moved on across the bottom of my feet and now seem to be knocking on the door at and above my ankles.

So....you don't have the hot and cold symptoms. That is rewarding. I generally have ice-cold feet and hands as opposed to hot ones. It does seem like my sense of the cold is much more severe than my MFR therapists feel from the outside.

What was the "other kind of SFN test you had in 2014? I have only heard of the skin punch biopsy test. I also have not read any post from a member with feelings that appear to end up in your mouth. A question. I do not know how old you are but I would like to know if you have been diagnosed with Osteoporosis or Osteopenia. That is when my mouth issues came into play.

You mention your medication in 2010. Are you thinking that it started your SFN?

Would you be so kind as to share with me what you actually do to alleviate your pain and discomfort? Just to get us started I will tell you that I have two sessions a week of MFR, Myofascial Release Therapy. There are two therapists with me in order to be able to work on feet, hands, etc. etc. Without MFR, I wouldn't be driving or having any kind of a happy, joyful life.

Are you looking for relief, answers, and current research information? OR??????

May you be safe, protected, and free of inner and outer harm.
Chris

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Replies to "Good evening @laura163, and welcome to Connect. It doesn't look like I have to remind you..."

Hi Chris , thank you for your reply , my report states SFN testing results.... Tested for cooling and heat test were normal and laser doopler flare
imaging was normal

They done large and small fiber neuropathy

I am 58 years old , in immaculate health ..No Osteoporosis or Osteopenia...No Diabetes , No thyroid , No blood pressure issues , No autto immune , No RH , No Arthritis , No physical , or structual , mental , cognitive issues at all...No medical conditions at all...Very healthy ..except for what happened after I cold turkey off a med that I should of never taken ...My ex forced me to take it ...

I never took medications in my life , prior or since ...I deal with the pain as much as possible ...I was always physically active ...until recently ..the intensity seemed to get higher ..

You mentioned your skull feels nerve pain...

For me it's not on my skull ...it's inside where the brain is ..that's where I am dealing with all the nerve pain ...Whatever that's going on firing neurons , electricity, burning, or Pons and needles , or feeling of inflammation, or turns in to a chemical feeling ...whatever feelings inside my head it's transpired throughout my entire body ..literally head to toe ..not one fiber is untouched ...I don't have blood pressure issues , nor dizziness, or physical weakness , I sleep with a fan directly on my face body , as hubby likes it too hot innocent room..lol...that cold air fan or even heat don't effect me at all...

As far as the medication I took don't cause SFN ..it can mimic alot of diseases..but nothing more then that...it's been 12 plus years I been dealing with this ..as others I know are also suffering immensely from repercussions from that drug known as benzodiazapam...

I work from home , managing my own company this entire time ..But in chronic pain

Can you tell me do you have the berne pain inside your head ? Or it's just on the skull ?

Do you have any other medical issues ?

Do you take medication?

Thank you for replying greatly appreciated

Have a great night