Pins and needles all over body, numb legs & back pain!!
Posted , 27 users are following.
Please help? - It all started 2 weeks ago, sat watching TV with a sudden bout of pins and needles in my right arm, this quickly progressed to my whole right side, after calling 111 they sent out a ambulance for suspect stroke - after tests this was not the case.
Next day i had P&N all over my body in different places, followed by numb aching legs and headaches 2 days after that, now most days i have pind and needles in my arms, hands & legs and the odd day I suffer with really heavy weak & numb legs that lasts about a day at a time then goes?
I have also been suffering with severe back pain in upper and lower back - seen the doc who has run bloodtests but all came back fine?? she is now stumped!!??
I have now been booked in to see a Neurologist in a weeks time but this is driving me crazy with worry as have a wife and 3 very young children to support as well as being self employed - anyone with similar symptons or help?
2 likes, 32 replies
alan35503 phil49742
Posted
Best Regards
Alan
phil49742 alan35503
Posted
marey phil49742
Posted
you can get a spray in an oil base too just max out on iy til your symptoms go...not poss to overdose ...you just get the runs...often a relief in itself!!!!!!!!!!
phil49742 marey
Posted
marey phil49742
Posted
Do you have an objection to trying to take high levels of magnesium? There is a high possibility that this could help....and defend you from further aggravating symptoms. You have a high burden of responsibilty. Have you got enough support and outside people you can talk to?
joanne47212 phil49742
Posted
richard89308 phil49742
Posted
richard
kerry1986 phil49742
Posted
Have you taken any anti-biotics recently? I have similar symptoms to you and have for over 4 months now, I have been diagnosed as a 'floxie'. Just a thought...
justme67 phil49742
Posted
Maybe ncs , nerve conduction study and mri to see if trapped nerve,
Ive recently had both tests for numb leg, not too bad,
Hope they sort you.
maria98868 phil49742
Posted
nadua007 phil49742
Posted
I hope you have recovered by now, but just want to share my story since I found the cause of it the hard way. I had all of your symptoms for a couple of months after breaking a metatarsal bone and sleeping only on one side for a few months.
It truned out to be a really bad misalignment of the joint between occipital bone and atlas putting my nerves under pressure at the top level making me feel pins and needles all over my body. A couple of adjustment by a chiropractor fixed that problem.
Best,
nik43413 phil49742
Posted
kae99906 phil49742
Posted
I've been having exact same issues, dont know what to do about the pain. Would please post it when you find out what to do and why we are have it
Thanks
magali34165 phil49742
Posted
Hi realize its been a year since your post, but i figured I give it a try. I hoping your story turned out good to give me hope.
I am having a very bad morning today. I suffer from anxiety. SO at the begining of the year I went to see a Nuero and I got a MRI with/out contrast. He called and stated that my MRI came out fine, ther was a lession that was there but was also found with normal patients all the time. But I just couldn't shake off the lession part. So 2 days ago I went to the nuero that ordered my MRI, and I wanted him to go over my results again beacuse I wanted to understand it more, turns out my insurance no longer covers me to see him, I have to see someone else. However I was able to obtian the report. And it says as follows?
1. Tiny t2 flair hyperintense foci within the subcortical white matter of the left frontal lobe just above sylvian fissure not associated with mass effect,restricted diffusion, or abnormal cnhancemnet. This focus is nonspecfic and can be seen in noral patients.
2.Otherwise, normal apperance of the brian
3. mild nasal septal deviation
BUt I of course googled the terms and this lesions are seen in patients with MS. I took this report to my genral dr, and she suggest a second opionion. I am just freaking out here. A normal person would pro read this and think ok I am fine, but me no! My anxiety level has gone up to DEFCON!
I still feel the tingleing in my left arm, and muscle weakness in the same arm.
I feel lighthead all the time
trouble sleeping
my eyelide has been twitching for past month
These symptoms are comperable to Anxiety and MS.
SO My mind is just running away with me.
Has anyone gotten a misdiagnoses before where they said it was fine they turns out it is MS?
Help Please
Jan1113 magali34165
Posted
I was wondering if the neuro followed up with an EMG. I'm having similiar symptoms, however, my recent EMG indicated nerve damage. Right now I am searching for a cause in order to stop it from progressing. The whole thing started last summer with the pads of my feet feeling puffy. I attributed to humidity. This was followed by cramping in hands and legs. Then came the twitching and pulsating. Two visits to my PCP in December and March and was told it was restless leg. I ended up in ER due to the combination of Parkinsons drug and muscle relaxer combination I was given for RLS. The ER doc could visibly see the pulsating through my jeans. At that point I was told I had PERIPHERAL neuropathy and had to follow up w a neurologist to determine a cause, To make a long story short and 6 specialists later (none of whom could provide a reason for the pulsating), my nights are a horror show and anxiety builds due to sleep deprivation. I'm in no position to lose my job. I still question the MS even though this is called CENTRAL neuropathy because of the brain. With this drastic change in my lifestyle, I realize that if I don't work on the anxiety, things will never improve. When and if you receive this, I certainly hope you are feeling better and found some answers.
magali34165 Jan1113
Posted
No I haven't. I see a second nuero for second opinion August 12th.
So I guess we will see what they say.
Jan1113 magali34165
Posted
Same here, was referred over by my neuro to another for 2nd opinion. Haven't gone yet but something about the possibility of a "nerve biopsy" was also mentioned.
wayne75607 magali34165
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Hi there.. just wondered if you ever found out what was going on with you? Your symptoms sounds just like mine was shocked when I read it tbh.. i have had an mri and mine was all clear but still things are getting no better and my doctors just don't want to know..
Thanks