Carpal Tunnel :: Thenar Eminence - Muscle Weakness After CTS Surgery
May 19, 2015
I had Carpal Tunnel surgery on my left wrist at the same time as ulnar nerve transposition surgery. Both healing nicely. My symptoms were not severe but I did have muscle wastage of the thenar eminence on the left side and slight weakness of the grip muscles. My concern now is that the thumb muscle is completely useless; can't grip, bend, carry. Nothing.
Is this normal after 2 weeks? Please advise as having right wrist done in 4 weeks and obviously don't want the same effect on right hand!
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Help! In 2001 I had a thyroidectomy. Immediately, my blood pressure, (which had always been remarkably low), shot through the ceiling and I've been on BP meds ever since. But I digress...
I was always super active. I skied, ran, kite boarded, hiked, biked... all a healthy and important part of my life. I even had booked a trip to climb Kilimanjaro for my 60th birthday in 2010 when I came down with Swine Flu, followed by a couple bouts of pneumonia. When I recovered, I tried to go back to skiing about three months later and found that I had lost muscle strength! I couldn't make turns (and that's a bad thing...) I got weaker and weaker. My doc had no clue. We checked heart, lungs. I was at low end of thyroid and adrenal levels, but "not a problem", I'm told. I'm not a drama person at all, but I really began to believe I was dying because I was getting weaker and felt like my energy was draining away.
At wit's end, I went (for the first time) to a brilliant naturopath who drastically improved my already good died and put my on Chinese meds. It took about three months, but I eventually stopped getting weaker and became stable. That was HUGE! Since, however, I've remained pretty stable and we keep trying other things but nothing has put me even close to where I was.
The best guess is that its related to thyroid or adrenal function. I dunno...
I can now make between 6-10 stairs before I have to stop for a few seconds to regroup. I can swim very short distances but never alone because when I run out of energy, its GONE and I have absolutely nothing left. This has drastically impacted my life and I want to be strong again!
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Went to doctor today in Dallas, Texas. He and his assistant were both rude. Had surgery 4 weeks ago and told him
my hand till tingles. He said it may take a year to be good again!! Had carpal 20 yrs ago and when surgery was over, my hand never hurt again!!! I cannot stand this for a year!! what can i do?
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Anyone having a feeling of growing pains in the arm, like the kind you perhaps had when you were a little kid growing up? I have had it for the last couple of days for some reason. I wouldn't call it muscle soreness after doing physical activities. The arm feel a bit weak.
I have intensified the massage of the forearm and upper arm, since I've found I still have some very tender points on the arms around the elbow, especially the right one then. My shoulder is crunching a lot and not as moveable as I first thought, so I've discovered.
Background history is herniated disc in the neck, broken shoulder, tennis elbow, broken wrist, broken long finger and now then carpal tunnel syndrome and then release in March 2014. All on my right and dominated side. Maybe this history background facts can affect you when you grow and get older?
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The doctors put me on gabapentin he said 1 first night 2 second 3 third day then carry on 3a night 300mg I took one first night befor bed slept good 2 last night and couldn't move when I woke up my back was in agony this morning any suggestions he said take at night time I explained I have a toddler and wnt take tablets that will knock me out when caring for my children , im supposed to take them for my arms as got carpel tunnel again and arms keep going into spasms.
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I had surgery 10 days ago and had my stitches removed yesterday. The nurse wasn't able to get one out but told me that she was going to trim it right down and it would most likely work it's way out. This morning I woke up to find some fluid not blood had been leaking from around the site of the stitch that was still in, it was also white and the wound red and hot, should I see someone about this or is this normal ?
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I had my surgery carpal tunnel syndrome 7 weeks ago on my dominant right hand. My job requires a lot of manual handling with adults with learning difficulties and pushing of heavy wheelchairs therefore I am still off work. I am in constant pain and scar area is solid and tender feels lumpy. I started physio exercises 2 weeks ago and hadn't really done much before that except wiggle fingers as I had not been given any advice at all post op. 2 weeks ago I couldn't even make a fist or reach my thumb to each finger, now I can make a fist and touch all finders and am using it normally but with a lot of pain, more so at night and shooting pains, my grip is extremely poor which worries me after this length of time. I am scheduled to have my left one done in around 6-8 weeks but I am now considering cancelling as I worry constantly that this will not resume to 100% mobility. Has anyone had this problem after this length of time? and did it improve up to 12 weeks post op?
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I was just curious if anyone has had persistent ring finger numbness? I've had ct symptoms 6+ years that come and go, however, now I have this strange numbness that won't go away... primarily in my fingertip (ring finger).
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I'm 25, and have recently developed symptoms (last 2-3 months). I had some mild sore wrists before but over the last few month it progressed to numbness in both hands. I did some physiotherapy and stretching and it did actually improve a bit but then my left ring finger began to develop pain and severe numbness, enough to stop me from typing with my left hand. I ice it several times a day which is keeping it at bay but doesn't do anything for the numbness.
Any comments or advice? I'm on a 1 month wait for an EMG specialist. The only thing that makes the numbness better is bending my wrist into a flexed position and holding it there for a few seconds.
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So I've had constant pain in my wrist for the last 6 months, more often when I bowl, it's very sharp pain and the more i bowl the more it hurst, it also hurts when I lift things as well.
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Anybody else had severe pain in wrist and new bruising 11 days post op. no issues with movement of hand or scar. Just this horrible pain when i put any pressure on my wrist.
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For the past 18 months I have experienced joint & bone pain, predominantly in my fingers, hands, wrists and elbows but also affecting my forearms, feet, ankles, knees, hips and shoulders. I have spent months trying to ignore it and at other times have kept detailed diaries, but can find no pattern relating to the area and level of pain and what I may have been doing, eating, drinking or how well I've slept.
I am nearly always fatigued ... I do work hard but even when I have time off, I'm exhausted to the point of needing to nap or walking around like a zombie. I used to run a lot and completed marathons, but now can't face a short jog.
Whenever I go to give blood, 4 out of 5 times my blood is too low in iron. It's not considered a dangerously low level for me but it is too low for the blood service to accept. The last time I went I succeeded in giving blood but was borderline and they only just accepted me.
Diarrhea; like many women I usually have this around the first couple of days of my cycle. However in recent months this is happening more frequently. Again there is no pattern relating to what I eat, where I eat or who prepared it. When it happens I get cramps and an urgency to go, but no nausea, sickness or loss of appetite.
Finally, I've recently begun getting pins and needles in one hand / fingers in a pattern that suggests carpal tunnel syndrome. It lasts for a few days then fades.
All of these things could be related or entirely unrelated, I just don't know. Also, one or two on their own might be easier to deal with but combined they can really get be down. My doctor has recently given me blood tests for arthritis and they came back normal. Any other ideas please?
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Although I try to be as active as possible my muscles are making life for me difficult, as for years they have been wasting, causing pain and tiredness. All other symptoms point to Fibromyalgia, which I believe doesn't cause muscle wasting.....also have Osteoarthritis. My muscle problems started in my mid. 30s.....am now 63 and is much worse. Recent blood tests show normal muscles values....but something must be wrong as my energy level is very low. Has anyone been /going through the same??
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for the past week I had severe joint pain and weakness, muscle weakness, bone pain in extremities ( had a blood test for lupus and RA[ no family history of either] Starting to get a bit better as long as I rest. recently sexually active with one person, now I just noticed feeling swollen like I was getting a UTI ( hurt when I urinate), but noticed it hurt in my vagina not urethra, checked and there are 4 small red bumps in my right labia minora and 1 in my left labia minora-odorless, feels inflamed and hurts now. Is this related to possible lupus or separate problem? I feel exhausted and run down.
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for a few days candesartan was helpful then the side effects set in. especially dizziness and arm muscle pain and elbow joint anyone else have this problem
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I've been having muscle weakness and burning in my arms and legs and back for about 8 months now and am so afraid that I have als or ms. I was wondering how long does it take for als and ms to manifest ? This is causing me great stress and depression.
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The last 2 months I've had tightness in my left buttock while on Prednisone. For the first while I could walk if off but for the last month it is constantly there but only when I walk, and sometimes shifts to the left leg's inner thigh, the result being I find I'm sort of limping. Has anyone had something like this? It could be a disc in the lower back pressing on a nerve affecting the muscles in the buttock and thigh, or maybe it's just muscle weakness resulting from the Prednisone. I'm in a quandary how to tackle it, see a physio, chiro, massage therapist. I've found that since I've had PMR 2 years ago anyone working with their hands on me greatly aggravates things so I'm unsure where to turn.
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I am a 29 year old female and I was diagnosed with Hashimoto's Thyroiditis at the start of the year. I have been having problems with my right eyelid in that over the course of the day it progressively becomes droopy and the only thing that relieves it is when I close it. When it becomes droopy it makes my eye feel like there's something in it and I end up rubbing it. It's only when I look in the mirror that it's droopy.
In January my endocrinologist ran an autoimmune profile (but not for every single antibody) and rheumatoid factor and these are the results of it:
Rheumatoid Factor - 9IU/mL (<20 negative)
HEP2 - Positive
Type - Speckled
Anti-DSDNA - 7IU/mL (<30 negative)
(Positive antinuclear antibodies but no significant disease association found)
ENA screen - Negative
Autoimmune profile
Antinuclear Abs - Positive
Anti-Smooth muscle Abs - Negative
Anti-Parietal Abs - Negative
Anti-Mitochondrial Abs - Negative
Anti-LKM Abs - Negative
Anti-Thyroid Peroxidase Abs (Anti-TPO) - 141 kIU/L (<34 negative)
I am posting here because I have a suspicion that I have Myasthenia Gravis. Not only have I got the problem with my eyelid but I tried to follow some physical tests for muscle weakness such as holding my arms out straight in front of me and deep knee bends.The results of these home tests I did:
Holding out arms stretched in front for 60 seconds - pain in both arms when it came up to the 60 seconds and left arm dropped slightly
10 deep knee bends - did all 10 knee bends but the last 3 made my legs feel weak and shaky
5 sit-ups (sitting from lying down) - could only manage 4 sit-ups
I have an appointment with my GP on Friday and since this has now appeared I'd like to mention my concerns to them.
My main concerns are :
Wouldn't my endocrinologist have tested me for Myasthenia Gravis if it's an autoimmune condition? If so what antibodies would she have tested and would any of the ones I had tested have shown I have Myasthenia Gravis?
Who do I need to request to see to get a confirmed diagnosis?
If it is indeed Myasthenia Gravis would it be because my current autoimmune condition made it worse? I have read that this is possible and I became very hypothyroid yesterday as I had very bad Reynaud's flares when out and about.
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I was diagnosed about 4 months ago with Hashimoto's. I'm on 75 mcg of Unithroid. I've started having extreme joint pain and my hands are always swollen. Some days it's a chore to walk up the stairs at work. The only time I feel really good is in the evening about 7pm. Any suggestions on what this could be? Who do I see for my joints to rule out other autoimmune disorders?
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I was diagnosed as hyperthyroid about five months ago. I am so much better now however the tremor in my hands and the muscle weakness in my arms and thighs doesn't seem to have subsided (or even lessened) at all like the rest of the symptoms. I am really worried that these are going to be permanent problems. Has anyone else had tremors and muscle weakness from this condition, and did it eventually go away or should I be preparing for this to be a lifetime issue? If yours did go away, how long did it take and did you need to take any particular supplements or do any particular exercises to help?
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I've been worried sick about my health condition these days I can't function well in school. My arms and legs have been feeling weak and have been getting short but sharp cramps. They would also feel numb sometimes along with a tingling feeling. I also seldom feel some muscle twitching which are not painful.
This happened a day after a very mild workout. Since then I haven't exercised due to the weakness of both my arms and legs.
The results I've been getting from the internet had made it difficult for me to sleep and go out. I am terrified this could be ALS. Is there any chance, even a slight one, that this could not be something serious? I am almost convinced that this is ALS but I still have a small dash of hope that it isn't.
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