Pains In My Hands, Wrists, Ankles - Fibromyalgia?
Jan 28, 2015
I suffer from chronic migraines for which I have been hospitalised on several occasions and I have always had a 'bad stomach' which has been diagnosed as functional dyspepsia, IBS and colitis at various times of my life. Last year I started having really bad pains in my hands, wrists, ankles and feet which feel swollen. If I exercise, my whole body aches and I simply cannot do the things that used to be easy for me. I'm even having difficulty doing the ironing and chopping the vegetables. Having always been a good sleeper, I now have periods of bad sleep and I always seem to be exhausted. Until last year I used to go the gym four times each week and I'v always been fit. Now I'm a wreck.
I've been seeing a neurologist for my migraines and a gastroenterologist for my stomach problems but nobody seems to see the big picture.
Do you think I could have fibromyalgia?
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I was diagnosed 3 1/2 years ago. Many ups and downs. I've now been told - PMR in remission. Inflammation and blood count almost normal. However, I still have quite bad pains ( shoulders/arms/wrists/hips). Thought Dr said PMR was in remission!! Has anyone else suffered like this?
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Male age 49, started with pain in my right hand 4 years ago. Gradually transferred to left hand and now is what I would describe generally as a combination of burning, aching tingling and numbness in both hands, wrists and forearms. No other issues, aside from that in good health and do lots of regular physical activity.
Lived with the pain which has gradually got worse and probably is something like a 5/10 on the pain scale now.
Recent stressful domestic issues seemed to aggravate the pains so finally decided to see a Spine Doctor (I am a Brit but live in the Philippines where medical care is excellent, especially when they see a foreign face with bulging pockets !)
The Dr did all the usual physical tests and none of them replicated the symptoms and her diagnised me with Carpal Tunnel Syndrome in both hands, to which I said "Sorry Sherlock, it ain't CTS).
Ok, he said, go do an MRI, which I just did and have the results (results pasted at the end of this post)
Went back to see the Dr and he said that I need surgery (Fusion of C5 and C6).
So, my quandry now is should I believe him or should I try a different approach.
The first paste below is the original MRI findings and the second paste is a second opinion that I got from an independent on line service.
IMPRESSION: -BILATERAL NEURAL FORAMINAL STENOSIS AT C5-C6 SECONDARY TO RIGHT FORAMINAL DISC EXTRUSION ON THE RIGHT, BILATERAL UNCOVERTEBRAL JOINT HYPERTROPHY WITH PROMINENT SPUR ON THE LEFT. -CORD EDEMA, C5 AND C6.
Second Opinion
OPINION:
There is a moderate sized, posterior disc protrusion/osteophyte complex at C5/C6 causing moderate spinal canal stenosis, moderate compression of the cervical cord and cord edema. The segment of cord edema extends from the level of the C4/C5 disc to C6/C7 disc and affects the left hemicord more than the right hemicord. Significant bilateral foraminal stenosis at C5/C6 with compression of both exiting C6 nerves (right more than left) seen.
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I been having stomach pains to the point for about 3 months which is really scaring me a lot I went to the hospital I thought I was my appendix but it wasn't they did x-Ray and ct scan and blood work everything come out normal but they told me I have fatty liver I also had h.pylori but don't have h.pylori no more took antibiotics and also have gastritis but still they don't find nothing but I'm still in pain it comes and goes to me it feels like it's air in my stomach it goes everywhere around to my left side to my chest but it doesn't goes away. Lately I been feeling nauseous wanna throw up I just wanna feel normal again as I write this. I have discomfort in my stomach right side I can push down with one finger on my stomach and hold it, it hurts and it feels like it's burning I don't know what to do.
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MY GP recently prescribed Atorvastatin to deal with high(ish) cholesterol. I have been taking Amlodipine, Losartan and Bezafibrate without any problems but in the past 3 weeks since starting the statins I feel like crap - Nausea, muscle pains, kidney pains and total lack of energy.
The blurb with the statins indicated there could be problems with Amlodipine but I started taking them.
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Just an update following my GCA emergency trips to hospital a few weeks ago. Increased 2 weekly injections are working. However, I just have such, thin, vulnerable skin. My wrists and legs are covered in bruises. I just gently knock a wrist or a leg and huge blue bruises. Is this the drugs? My wrists look like I have been in handcuffs but all I have done is knock them getting stuff out of the washing machine, tumble dryer or dishes out of the cupboard.
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All been having a few new symptoms . numbness in face just one side and neck legs and around my wrists anyone else have these symptoms . also lent on my elbow its really gone sore very red and skin coming off something that has never happened before i used to bruise very easily before but nothing like this . i,ve been trying to find out what sort of help out there for me and not really getting anywhere i was wondering what sort of help others where getting.
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I'm a 20 year old university student struggling to cope with the constant pain and irritation of my eczema.
I get it all over my arms, armpits, neck, chest, the back of my legs and my wrists. Its scabby, sore and irresistible to scratch at. I have on too many occasions scratched it until i bleed but i really cant help it. I have had severe eczema all my life but in the past two years, it has really started to get me down. I have applied prescribed steroid creams, Hydrocortisone, E45, Doublebase.. showered and bathed in prescribed shower and bath gels and swallowed countless anti-histamine tablets in the hope of them taking away the itch and the urge to scratch.
I'm writing this as i am so fed up, just like the millions of others suffering from eczema out there, and hope that one of you out there can help me, or atleast give me some tips to reduce the irritation.
Currently i am applying Aveeno Skin Relief Moisturising Lotion after i shower. It does reduce the itch and calm my skin, but the redness and dryness returns when the cream is absorbed or whenever i start to sweat. I can't partake in exercise or sporting activities as i am scared, actual fear, of how itchy and sore my whole body becomes.
As i sit here repeatedly itching up and down my arms i'm hoping there is someone out there who can give me some advice, i've had enough of being embarrassed and fed up of my skin.
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Several days ago, I developed Edema (or Oedema) overnight in both my feet, ankles and calves up to my knees. This is my third bout of edema. The first was last year but only in my right foot and the second time was a couple of months ago, again in both feet and ankles but was very mild.
Two days later, the swelling became so severe, both my feet looked bruised and turned a funny red colour. The pain became that powerful, I couldn't walk whatsoever.
Im in UK so I rang 111 NHS helpline who sent out an ambulance. The paramedics arrived and were shocked as they had never seen edema so severe before. This was a Saturday and my GP closed so they arranged an appointment with an out of hours GP at my local hospital in the next hour.
He had no idea what the cause was and was that worried, he sent me to another hospital 30 miles away to see a specialist. I arrived and was admitted in straight away for tests and observation.
They took blood and urine tests, a chest x ray, a heart reading straight away. But they couldn't link a diagnosis with the edema. They flooded me with antibiotics assuming that it was an infection.
I was discharged the day after as the redness and pain levels seemed to have gone down a little after the antibiotics and i will be returning soon for an ECG and other scans. I left with walking sticks so that I could walk around easier .
Now today its been almost a week. I still need the walking sticks to walk, the swellings is still huge, the pitting is still evident but i do think the antibiotics is helping some.
But I really wish I could know what this is as its very worrying. The docs couldn't see a problem with my heart, liver or kidneys. I have also been tested for DVT and gout. My blood sugar is fine. The only possible resolution is that it cold have some link with the hot weather, but that wasn't confirmed.
Has anyone else had severe painful edema in both legs and the doctors couldn't find a diagnosis?
My current medications I take regularly are: Mirtazapine 45 mg and Hydroxyzine 25mg.
Can anyone advice or share their experiences? Is there anything I can do to help minimise the risk of this happening again? If this is heat related, I'm going to have a hell time every time it gets hot. But surely 'hot weather' cant just be the only explanation there is why I have major swelling in both my legs and feet.
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I have started on 50 mcg of Levo today after being on 25mcg for about 6 months, today I have noticed that my ankles are puffy and swollen, could this be caused by the increase in dose?.
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After finding I had high blood pressure a year ago I was put on Amlodipine I had really bad side effects with swollen ankles and a really bad rash.
My medication was changed to losartan 50 mg and Atorvastatin 20mg. Although this combination is keeping my Blood Pressure down. I still have a weakness in my ankles and a slight remaining problem with my skin on my ankles.
I would have thought these problems would have disappeared completely after stopping Amlodipine . But now I am thinking it's the statins that is stopping the side effects in my legs from disappearing completely.
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I have been taking Cialis for 5 days now, 5 mg, once daily for enlarged prostate.
Last night I got a bad back ache which I did not think was related to the Cialis. My back hurts literally from my shoulder blades to my ankles.
Can this possibly be from the Cialis?
Back pain with Cialis is listed as minor. This is a serious back ache, both legs and hips throb as well as lower back and as I said all the way up to the shoulder blades.
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My Father in law (72) is suffering terribly with his legs.
Had Diabetes for years but just recently his ankles have swollen terribly and he can hardly stand or walk. For someone used to being active, it's been a terrible time for him.
I watched him try to stand the other day and it looked complete agony. He can't understand why no-one can tell him what is wrong, doctors are saying "it's your diabetics, you have to expect it"...
His doctor won't give him extra pain management because he says it will impact his other medication, but I just don't see how he can continue with all this pain. How we get the best treatment as I don't think he is getting it at the moment.
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I have been suffering from a rash on my ankles. The major symptoms I would say are a very itchy rash that waters when I scratch, and more prominently, 'dead' skin forms around my ankle and peels. The skin also seems to be getting tougher (maybe due to the scratching).
I have been to 2 doctors so far. The first felt it was contact dermatitis and gave me a corticosteroid (mometasone furoate) which cleared it up for some months but then it came back again. I've been to another doctor 2 weeks ago who gave me an antifungal cream (daktarin), but after 2 weeks of applying, I can't see any significant improvement to be honest. In fact, the infection spread to the left ankle only after I had started this treatment. I don't know if there's a connection. I would be seeing a specialist next if this treatment fails but I would like to have a good idea of what it might be.
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Fractured and dislocated my ankle after slipping on a muddy path 17th Dec 2015 After 10 days bed rest and foot elevation in hospital to get the swelling down over Christmas I had 9 screws into fibula and a metal plate and screws into bone on other side of ankle. In a cast for 2 weeks then Xrayed and assessed and another cast put on for 4 weeks. Dissolvable stitches and ankle alignment satisfactory.
2 more weeks until consultant visit to assess maybe given a boot.
Very painful for a week after 2nd cast put on but settling down now. Using a wheelchair to propel myself around the house. Living downstairs but been upstairs 3 times backwards on my bottom pushing up with good leg wearing a trainer for grip. Good exercise!
Was initially given a zimmer by hospital but very unsteady and not confident on crutches. Will hopefully use them when allowed to put some pressure on injured ankle.
Some nights I have to take paracetamol particularly if the ankle has not been elevated enough during the day. I sleep a lot more but presume it is to do with the healing process. Drinking a lot of milk and a VitD pill once a day with plenty of protein foods which I hope will encourage bone healing.
Was very active but not able to do much apart from knitting and sewing. Try to do a bit of housework each morning but have temporarily employed a cleaner. Thankful it is winter and no gardening necessary yet.
Encourageing to see how other broken ankles progress. No physio for me yet but I do Pilates exercises each morning in bed before putting ankle down for another day.
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does anybody else get swollen ankles and feet when taking lansoprazole, is this a side effect of this medication. i would like to see some answers to this. and do you get such a dry mouth.
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Within the last 2/3 weeks, I have noticed welts (very large and warm) on certain parts of my body, mainly around my ankles, hips, backs of my knees, and one spot on my spine. At first, I thought it was an allergy to my laundry detergent, so I started making my own because I am allergic to everything else. After switching soaps, I noticed that the hives/welts subsided but then after a couple days, I got 2 on my spine again. One welt was about the size of a silver dollar and the other, about four inches lower on my spine, about the size of a quarter. Later that night, the left side of my lower lip randomly got very warm and started to swell. It looked as though I had been stung by a bee. There was no pain other than the uncomfortable tightness.
Any ideas on what could be the cause? I can't get into my doctor for quite some time, and I prefer to avoid the emergency room since it doesn't seem that serious but I'd really like an idea of what in the world is going on.
Update 12/16/13-This morning I woke up with one nickel sized welt on each arm, just below my elbows.
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I am 51, broke my left ankle on a hiking trip on Friday, had a surgery on Sunday night.
Generally things are getting better : much less pain, can wiggle my toes, but there is a persistent numbness on top side of big toe and second toe.
Looks like it might be some post-op nerve damage, because it is not getting worse and does not affect the mobility of toes. Decided not to go to emerg, that would mean sitting there for 6 hours before any doc will come to see me. But if it would become worse, then I would go.
Also : feeling very unsafe with crutches, in particular when home alone. Using a portable wheelchair instead for the trips to the bathroom, getting food from the kitchen, etc.
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I'm 4 months post op but the screw from the inside of my ankle to the outside of ankle is showing under my skin quite a lot. Does anyone else have this problem or is it not normal?
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Well the good thing is that now 12 weeks post ankle fractures in 2 places and dislocation I am up and about walking again which is the good news. The not so good news is that I have a slight limp (to be expected) but unfortunately I now have pain in my knee which is causing me to limp more! How on earth can I get rid of this knee pain which is counteracting my rehabilitation. Has anyone out there had a similar experience?
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A large number of individual and now merging spots/lesions over face ears, hair, ankles and arms. They are terribly itchy and have tried all sorts of creams etc. Gp says its scabies, have had medication for it, definately not as keeps recurring. I cannot go out, have been to a dermatologist who gave me pills which actually made me hallucinate and feel very ill?
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