Cramps :: Overuse Of Muscles
Jun 18, 2015
They started a week ago, two days after a very strenuous run and arm workout. I don't run a lot and the exercise really wore me out and my quads were sore for a couple days. Then I started getting cramps in my left forearm and left anterior calf muscle (above the ankle). They come multiple times in the day simultaneously for about 5-10 seconds then fade away together as well. I've tried every home remedy(massaging, hot bath, stretches) and none have affected the frequency or intensity of the cramps.
I visited a primary care doctor who drew blood to check my electrolyte levels and gave my head a ct scan, both came back normal and they wrote me a script for Flexeril which helps me sleep but does not relieve the cramping.
The next day I visited a neurologist who gave me an EEG to confirm I was not experiencing partial seizures. He then put me through some basic strength tests and confirmed I wasn't experiencing strength loss in my affected limbs and said he didn't think He referred me to another neurologist who specializes in muscles to "make myself feel better" who I'm seeing Friday.
I've been able to rule out some scarier stuff with the CT scan and the fact that I haven't been feeling any weakness (other than soreness), or other symptoms other than the cramps themselves. Maybe it's a slipped disc? That's the only thing I've read that makes sense. This seems like too long a period for something as simple as an overworked muscle
Long story short, all the doctors I've seen haven't found anything other than overuse of muscles and long cramping. I'm hoping anyone who has experienced something similar or knows someone who has can provide any advice or insight into what's going on. Thanks!
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Have suffered since childhood from cramps, mostly in legs but also in hands and arms. Now, in my sixties, suffer much at night with convulsive twitches in leg muscles or actual painful cramps - sometimes reaching my back up to shoulders. Usually accompanied by cold clamminess or hot sweats. When this happens sleep is not possible. Otherwise in good health.
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I was recently diagnosed with hyperthyroidism and I have been taking Carbimazole since Aug 6, 2010, since yesterday I have been experiencing painful leg cramps (not the usual night time calf cramps) that begin just above my right knee and travel down to my foot sometimes 5 or so in quick succession - this is really painful :? and I wondered if anybody else has these or should I go back and see my GP?
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Cramps so bad in thighs, I can't take the pain anymore
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I had what felt like ovulation cramps last week and tonight have vaginal bleeding, fresh blood not old.
I did this in 2012 after my mom died, was checked pap smear, uterine biopsy and I feel those hurt, it was all good, they thought it might of been stress related because it lasted only one day.
My abnormally normal periods were only 1-3 days, they were one coming in, one day of heavy bleeding, and spotting on third day. But every 28 days like clockwork with no issues there. In my 20's I was told I had endometriosis and when they went to do the ultrasound the cyst had went away. I didn't take it any further than that but never had children and never took birth control. Cramps were always very painful, had to curl up in a ball, always had severe back pain with them as well.
Last week they were like that not quite as bad but nearly.
Is this just a fluke you all think? Even menopause I had no symptoms, when I turned 50 it shut off like a faucet never again until 2012, and now.
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I'm having a hard time distinguishing between cramps from the intestines/stomach and slight cramps from my "female parts"... Sometimes I think that I have a regular stomach pain, but I'm wondering whether the pains could be slight cramping from my uterus instead? Right now I'm most likely just passed the ovulation and should have my period in about 13 days. Would slight cramping during this time be normal for someone in perimenopause?
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are there any exercises to help with strengthening paralysed muscles resulting from deconditioning after illness. breathing very weak fast and shallow and very frightened of respiratory failure. Doctor unsympathetic due to previous mental health diagnosis and cant afford private treatment
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does anyone have calf muscles that are constantly going crazy painful and keeping you awake
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I was put on this drug because I had a bad reaction to amoxicillin, I finished the course of these and just after that i started getting really bad headaches and it was affecting my eyes and also all my muscles started to get very painful,my neck and shoulders was the worse, my doc got blood tests done as he thought I might have polymyalgia but that came back clear so he put it down to a migraine, i've never suffered from headaches as bad as this one, this went on for 2 weeks and eventually it just went and all the pains went with it so after reading this i'm putting it down to these drugs and not a migraine. Has anyone else had a bad reaction after finishing the course of them?
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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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I have been dealing with anxiety for the last 4 months but woke up the other morning and both my calf muscles were sore lime I had run a marathon but of course I hadn't. I did feel anxious or anything but they say you can get the symptoms without having it and was wondering if this is anxiety symptoms at its best.
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I am 62 with Multiple Sclerosis. and it was boggling my mind that the legs were aching and pain just like i had just run 17 - 100 metre dashes.Thought it was MS but it just did not make sense(after 35 years i know my MS)...and then I had two days of Heartburn like a Volcano and found this Forum and read about Heartburn problems and Muscles Aching.
My question --- does anybody know absolutely for sure that there travelling aches and pains in their muscles are from Menopause-- I had to stop exercising as my legs were so sore....I do recognize after 8 years of exercise it is the key for a low maintenance menopause
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I have nasal polyps, but now my the muscles in my neck ache. I don't have a sore throat, except when I go to swallow. I get a very hoarse throat, daily. What could this be?
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I've been experiencing a feeling of tension/achiness in my muscles for almost a week....most notably along the sides and back of my neck, but also my arms and legs....even when I'm simply sitting down, they feel achy...I'm also exhausted by the end of the day and have a headache most days...all related? I do think I've been clenching my jaw a bit (right now, as a matter of fact), which I suspect is contributing to the neck and head aches (and probably my dizziness too)...but what about the arms and legs? Almost feels as though I can't use them (although of course I can)....they just feel very heavy and tired. I had a period (of sorts) last week (it was very light, and it had been a couple of months since I had one at all)....could that be the culprit? Anyone else feel this way? These symptoms are all making me feel as though I'm losing my mind!
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My symptoms are severe pain in joints and sometimes muscles that always come with high fever, sore throat and weird cough (small but forced cough) a salmon colored rash and weakness in my joints. The pain is so bad that I scream. I am unable to care for myself. I am so stiff for hours. The pain has progressed throughout the year. I am at a loss. I live in Idaho and my rheumatologist is sending me to Salt Lake City Utah because they have a university hospital with more specialist. I swear to her that I have Stills Disease but she sais I have the symptoms but not necessarily all of the blood results to match.
My cbc always shows an infection, I am always slightly anemic but ferritin is good, not low nor high.
Here is my recent lab work. This is how desperate I am
C-REACTIVE PROTEIN 60
UNITS = ML/MIN/1.73m2
If patient is African-American, multiply result by 1.21.
ALBUMIN 3.5 - 5.0 GM/DL 3.5
AST(SGOT) 15 - 46 U/L 37 45
TOTAL BILIRUBIN 0.2 - 1.3 MG/DL 0.3
CALCIUM 8.4 - 10.6 MG/DL 8.8
PROTEIN TOTAL 6.3 - 8.2 GM/DL 6.1
ALK PHOS 38 - 126 U/L 37 78
ALT(SGPT) 9 - 52 U/L 37 50
ANION GAP 7 - 15 MMOL/L 8
CK 30 - 135 U/L 37 24
I do not like being on the prednisone because of the side effects but I can not handle the non stop pain when I don't have it. Such a little 5 mg dose saves my life. The pain is so bad that all I can do is pray to pass out. I can not take pain pills because they cause severe depression.
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My face is puffy, tired, dry; Head feels heavy; Cognition is not working properly; Muscles are sluggish; Energy levels are low; Constant sleepiness... Tons of visits do docs - everything OK. Tons of supplements and drugs - no effect. Free of thyroid, sleep, vitamin, blood, organ, allergy, lyme, hiv, virus issues etc. You name it. Started along with stressful period 2 years ago. Could it all really be some mental issue creating havoc throughout the body, i.e. psychosomatic? 21 years old male.
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I have been on 400mg of Plaquenil for 7 months now, but for the last 2 months I have been experiencing muscle problems in my legs, it is so painful that I am yelling out with pain. I stopped taking the Plaquenil and the muscle problems stopped. My GP (American Dr) advised that the Plaquenil was the cause of my pain, although my GP (English) advised that he did not think it was the medication. I am now confused because once I stopped the medication my pain went away? I am now waiting to see my RA but have been waiting for 2 months now, and been on no medication since. Now my bloods are really high again and all my pains and symptoms are back. As anyone else had the same issue with this medication?
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After numerous medical consultations and exams I finally was referred to Addenbrooke's Hospital in Cambridge to a specialist in the audiologist department.
It appears that I have an issue with the Stapedial reflex muscles. This causes me pain resulting from normal level sounds.
They have prescribed relaxation and sound therapy rather than surgical treatment at this stage.
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I am now into my 7th week on pred just reduced by 2.5 mg and have noticed that my muscles in my hands are starting to lock, it does not last long but are becoming more frequent and painful.
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I've just had a blood test which showed vitamin D deficiency. I have very little energy, my muscles and joints are stiff and painful, and my feet really hurt when I try to walk any distance. I've always been very fit and active so I'm wondering whether I should push myself to exercise even though I don't feel like it or whether I risk making my condition worse by pushing myself too hard. I'm taking vitamin D supplements but I've seen from other posts on this forum that it might take months to get better. I find swimming less painful than walking or cycling so maybe that is okay?
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I've just been diagnosed with Graves disease. I am taking Carbimazole 40mg daily now, for 8 days. I have the dreaded 24hr sweats - aching leg muscles - sleeplessness - no energy and lie on bed for most of each day!
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