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pin pricks, electric like sensations all over
ok, I'll try here.......I have also appeared (even though I am invisable) in the Fibromyalgia postings. Had no responses. I have pin prick sensations all over my body at different times, thousands of times a day. Also have water feelings and buzzing on legs and feet at times. Have had every test known to man. The neuro said I do not have neuropathy because I have no sensation loss, only "positive" sensations. Well, they are not positive in my book, I feel like I am going to lose it!!! I am on 900 mg. of Gabapentin a day, it worked for the last year, but lately I am having more breakthroughs.
The neuro basically told me he has no dx. for me, he said he sees people like me about once a year (I feel like a freak of nature.) I am a 52 year old female. Does anyone have or know anyone with this or even have any ideas on what this could be?? Please, I could use some encouragement feeling glad I don't have a serious dx. but very upset to have to deal with this 24/7. P.S. Also get a lot of muscle twitching (not cramps), just twitching! |
Hi "Invisable" ~
Jeepers ~ how frustrating! I get all those things too, but I have a diagnosis! Have you had an MRI of your spine? If so, can you read it to us? Do you have one of the cervical or the lumbar? Or both? If you DON'T have an MRI, you should have one done, with and without contrast material. I'd be interested in seeing what it says, if you have one. Thanks alot. Hugs, Lee :D |
Hi Leesa-tx for reply.......
Quote:
I also got an MRI of Thorastic Spine, again nothing related to sym. I have not gotten one done of Lumbar area of spine, I wonder if my problem is there, but would I have symptoms above that region or just below? Would you mind sharing your exact symptoms with me and your dx? If not, I understand. |
i have degenerative disk disease, scoliosis, lordosis, herniated disk, osteoarthritis, osteoporosis, severe sciatica (permanent) and peripheral neuropathy. LOL My right leg/foot twitches, stings, burns, feels like there's water running down it, and is numb at the same time if that makes any sense. Plus there is severe pain. Now I KNOW that doesn't make sense, since it feels numb, but there it is. The pain feels like it goes all the way to the bone. My doc just switched my med to the fentanyl patch and I'm not doing so hot. :confused: I think he and I need to "talk." LOL
I don't mind telling what I have - my life is an open book! Hugs, Lee |
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I just went to another neuro today......he wants me to get a skin biopsy, thinks I may have non-length dependent peripheral neuropathy. I have heard of neuropathy that people have just in feet and hands and sometimes cannot stand sox or shoes or bedsheets touching their feet. What does someone do with it all over body? I may have to join a nudest colony!! There I go joking again.......so I don't cry!!! How progressive is neuropathy, I wonder........ Mine seems to be getting worse, or I am building a tolerance to this Gabapentin (900mg/day) If this keeps up, I will be on morphine in no time! |
I really don't know how progressive the neuropathy can get, but keep in mind that you can go UP in the medication A LOT MORE!!! You are on a "relatively" low dose. Personally, i don't like that medication cause it causes fluid retention - and it made ME feel "loopy." LOL I'm on Topamax, which does the same thing.
Jeez, I sure hope yours doesn't keep progressing!!! Mine is bad enough and has now spread to my other leg after 25 years. Good grief, I can't imagine having it ALL OVER!!! Bless your heart, I'll keep you in my prayers, for sure! Keep me posted on how you're doing, will you?? Big hugs, Lee |
Re:pinpricks
I had those symptoms of pin pricks, and electric type shocks on my arms. I did have herniated disks and was recently fused C3-7. I was told that these symptoms were indeed from my neck. Maybe it would be good to have another opinion. I never thought I would get relief, but I did. Good luck to you. ginnie Don't give up:hissyfit:
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Virginia ~ if you were RECENTLY fused, then INDEED get another opinion!!! There might be something associated with your fusion!! Please - get a referral to another Neurosurgeon. Something might be going on. God bless. Hugs, Lee
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electrical stinging entire body
I took a lot of levaquin but my entire body stings with intense electricity like electrical raindrops. and most days to the point of screaming.. My entire body is like this. even face and head.. Then I found out I have morgellans on top of this.. I did not even knew it existed. I have tons of fibers coming out my body and stool.
I have heard of people having stinging but this has an INTENSE electrical component to it.. I cant wear clothes. I just pace and cry. They even tried IVIG on me and I reacted horribly. Does ANYONE have this over entire body with such intensity you want to end it.. No one knows what is wrong with me. I have searched the internet over and NO ONE Stings to this degree with the electrical conponents.. Feels like millions of bees on me all the time.. |
Hi Rykerjem,
Welcome to NeuroTalk! :D Wow. I am sorry you are in so much discomfort. :( I know that's an understatement. :hug: You may find it helpful to check in at the Peripheral Neuropathy forum: http://neurotalk.psychcentral.com/forum20.html The PN forum is very active and has some very bright minds working on medical issues like detectives. :) You may copy and paste your written post there and/or write a new one. It will be helpful if you start your own thread there, so you will be seen right away. People will get to know you-- will ask questions and give feedback. Please also make yourself at home on any of the many forums here! :) To Our Healing, DejaVu |
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