Polymyalgia Rheumatica :: Numbness, Pins And Needles In Feet And Legs
Sep 1, 2015
I had a mini flare 10 days ago and went up from 8 to 9 and half. The last two days I have had extremely uncomfortable numbness and pins and needles in my feet and lower legs. The numbness is so bad that I scratched my leg on my zip and drew blood, but hardly felt a thing. I have a bright red weal there now.
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I have numbness in my left upper leg once a week, to the point where I cant feel anything when I touch the skin on my leg. I also have pins and needles in the same leg. I don't have any pain. I also have a slight case of scoliosis. Its not visible but it might be a contribution to the numbness in my leg?
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I've had anxiety for years and most of my family suffers from it. Recently I've been having pins and needles, burning feeling in my hands or feeling of numbness in my fingertips. When I wake up in the morning I feel very shaky inside and today I've felt my legs shaking throughout the day and feeling weak. I'm feeling so overwhelmed by it and convincing myself I have MS. It's literally preoccupies my mind throughout the day and I feel like I'm driving myself crazy checking for symptoms. I've been seeing therapist for years and I've been fine for years but for some reason it hit me hard again beginning of this year. Does anyone have similar symptoms?
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I'm not sure Wat it is I have I have numbness in both feet and lower legs but my knees are in constant pain and buckle on random occasions or if I try and jog/run at the start of this I was detoxin of of alcohol addiction and that's when it started i've had and mri of my head and back bloods etc and all seems OK so it's leaving me and doctors scratching their heads?
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Have had PMR for 18 months, down to 5 mg. pred/day, just bumped up to 6 mg. in an effort to mitigate pesky edema in lower legs, ankles and feet. Me: 65 yo. male in Florida.
Edema is gone in AM, before rising, then gradually increases over the day to a 1+ to 2+ grade (moderate, when pressed with finger a 2-4 mm depression remains for 7 to 15 seconds).
Had Hands and feet involvement pre-prednisone, no apparent joint degradation from RA, not diagnosed with RA. Rheumies have given me blessing to make minor adjustments in dosage and taper to mitigate symptoms (you know what I mean).
Any out there have experience with this particular manifestation? How did you deal with it?
Thanks to all in this group. I may have not said it before, but you who contribute often, selflessly, with considered information. are a stalwart foundation to those of us in the silent majority.
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I've started taking 25MG of nortriptyline for migraines- my dosage goes up to 50 MG at the end of the week. The first few days of taking it, I experienced physical exhaustion and grogginess, as well as numbness in my legs, feet, and hands, but nothing too bad that impaired me. I also have felt more mentally focused. Any thoughts?
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Diagnosed with PMR & GCA in December, 2015, I am down to 40 mg prednisone together with 20 mg methotrexate. Have only been on the methotrexate for 3 weeks and down to 40mg of prednisone for 2 days from 42.5mg so far so good. Apart from the normal side effects of prednisone, I am experiencing numbness in the tips of my fingers which spreads down into my hands. Mostly on the left side which is where my GCA is worse.
However, sometimes I have it on my right side as well. I have no strength in my hands and am dropping things. I have spoken to both my GP & Rheumy and they have not any answers. One would presume it is to do with blood/oxygen flow.
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Getting pins & needles in hands and feet, on 25mg for 5 days now. Anyone else had this? It's really annoying... IS it normal?
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Ten days ago I had a robotic laparoscopic myomectomy to remove four large fibroids from my uterus. The surgery went great, and I've been recovering at home and have been waited on hand and foot by my husband a bit less each day.
The only problem I'm having is occasionally in one specific spot I'm experiencing a pins and needles type of pain - sometime like shards of glass - in my abdomen. Yesterday I thought it was the result of overdoing it so I rested yesterday and still woke up in pain. My doctor is an hour and a half away (closest one I could find who does the Da Vinci robot!) so I'd hate to schlep myself all the way there if I don't need to. Anyone have any insight about this kind of pain following surgery?
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I've just taken my second tablet of the day about 20 mins ago and I'm having serious side effects. I've been on them since Thursday and have had a few issues with shaking, palpitations, insomnia and some mega weird dreams but nothing I couldn't cope with. in fact nothing I didn't have in one degree or another before.
Tonight I'm in serious pain with my chest. My heart feels like it's breaking out and breathing is hard. I'm light headed and dizzy when sitting but when I lay down my head starts pounding as if all the blood is being pumped in there.
My legs feel numb and everything below the knee has pins and needles.
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I have been taking this medication for nearly 4 weeks , the first 2 weeks with prednisolone as a treatment for nasal polyps. I am spaced out most of the time , have had weakness in my muscles, pins and needles and numbness in my fingers. My stomach was painful so I have taken omeprazole for that which eased that pain altogether. Clarithromycin also have me insomnia and mood changes. They made my skin greasy,eventually spotty, and I have headaches and think I am sensitive to the light.
I finish them in 3 days time thank the Lord. At times I felt like passing out and unusually for me zonked out at unlikely moments during the day.
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This has left me with pins and needles in my knee which is very painful at times. I do have a bit of arthritis behind the knee, if anyone else has had this problem does the cream called flexiseq work ?
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Been on Ramipril for 2 1/2 years, always suffered froma bad cough with it, most annoying. Saw new Dr few months ago whos took me off ramapril because of cough. New tablet (evil drug) called amlovasc terrible side effects, pins and needles to the face, legs, and arms, severe tiredeness, swelling to ankles and knees. Took myself off these tablets. Going back to GP tomorrow morning, prefer to put up with the cough
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My daughter was born at 32 1/2 weeks and has very mild cerebral palsy, she is now 17 and experiencing days when she can't get out of bed. She is just exhausted and gets pins and needles. The doctor suggested it could be ME but I wondered if its a result of her Cerebral Palsy. Every time she does something that requires more mental or physical input than normal she is then wiped out for 2 days. Her CP has never really affected her, she wore Piedro boots as a child but recent years has had a "normal" life. Would really appreciate some input, she is due to have an MRI next week.
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I have been taking 1800mg of Gabapentin (600 3 times daily) for less than a year now to help with my nerve pain. It was working well however in the last few weeks, I have noticed that shooting pains and the pins needles sensations have started to return. Is it possible I've built up a tolerance to gabapentin? I wanted to check in here first before going to my Dr to see if anyone else had had the same experience.
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I have been taking Simvastatin for over two years. During this time I have got progressively worse. Started with tingling and pins and needles in hands and fingers, sore sole of the feet and a little bit of joint stiffness, lumpy legs, severe lethargy, tiredness and irritability.
NOW I have muscle wastage of the shoulder muscle, severe joint pain in spine, chest, hips, wrists and fingers. I have lost the grip and strength in my left hand, finding it difficult and clumsy to use. My sight is progressively getting worse, I feel as if I,m looking through a slight fog. My memory loss was becoming a real problem. Diarrhea, chronic muscle spasms - I was beginning to think I was going to die.
I have only just been made aware that the cause could be Simvastatin - stopped taking them 5 days ago and I am feeling a little better having good days and bad days.
My concern is that if these problems have been caused by Simvastatin - it looks like they could be irreversible!
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I have been using Lansoprazole for nearly 4 years, I am on 30mg daily, it works great, and I rarely get heartburn these days.
However I have for the past year been experiencing severe lower back pain, pins and needles, strong headaches and more recently dry mouth and dizzy blurred vision.
I stopped taking the Lansoprazole for couple of days, to see if side effects would go away, but the heartburn came back with a vengeance.
So I am having to choose between which is more unbearable, back pain etc. or the heartburn.
I have chosen at the moment to go back on lansoprazole, but if anyone knows of an alternative that works as well, but with no side effects, let me know.
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I have been on 20mg Fluoxetine for 6 weeks and the past week I have been experiencing tingling (mild pins and needles sensation) intermittently in my feet, legs and hands. I have had other anxiety related symptoms and this is just adding to my anxiety.
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Anyone else get red feet, or legs from sciatca?
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I am a teenager and my legs get so purple almost like a veins all over my legs. They also get really splotchy. My hands and feet get purple and have splotches. My feet turn splotchy only when i'm sitting or standing. When I get really hot everything is normal. I hate wearing shorts or anything that shows my legs.
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I am a 40 year old male about 30 pds overweight. I developed sixth nerve palsy in February 2014 and it finally cleared up three months later on its own? In July 2014 I started burning in my left arm and hand. As time has went by until now the burning has got worse in both feet and legs up to the knee. I also burn in both arms and hands. I burn across my chest and left shoulder also some. I have had several blood test, MRI, nerve electro study. The Dr. Found that I failed my oral glucose tolerance test twice and a skin biopsy showed small nerve fiber damage. I am currently on metformin 500 mg 2 x a day and gabapentin 300 mg 3 x a day. The gabapentin doesn't help. I have taken lisinopryl hctz 10- 12.5 mg and citalopram 20 mg for several years, could the burn come from these medicines? Is it because of diabetes 2, even though my a1c has been only between 5.6 - 5.9? Any ideas on the cause or what to do?
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