1. Health
Send to a Friend via Email

Discuss in my forum

Adrienne Dellwo

Impaired Coordination in Fibromyalgia

By February 15, 2013

Follow me on:

Research Brief

A recent study revealed problems with fine motor control and manual dexterity in fibromyalgia.

Participants performed tasks such as writing, turning over cards, placing a pin, stacking checkers, and picking things up. The fibromyalgia group was slower with both hands than healthy people in the control group.

Participants were selected in part because they didn't have fibromyalgia symptoms in their arms and hands, so researchers concluded that the deficits result from an underlying central mechanism that alters motor control.

My Perspective

I know my hands don't work like they did before fibromyalgia. I drop pills all the time. I have trouble separating papers. Threading a needle has become an exercise in patience on good days, and an exercise in futility on not-so-good ones.

Fibromyalgia is linked to dysregulation of the neurotransmitter dopamine, which causes movement problems if it's out of balance in the movement centers of the brain. So far, we don't know whether our dysregulation includes those areas, but my own belief is that it does. Time will tell.

Do you have problems with your hands, or coordination overall? What is hard for you? Leave your comments below!

NEWSLETTER | FORUM | BIO | TWITTER | FACEBOOK

Comments
February 15, 2013 at 8:03 am
(1) Ankur Mahajan says:

Definitely.Actually, this was one of the earliest of symptoms. I used to play football and I was quite good but once I started playing football again, I was unable to judge the ball.Also it was quite difficult for me to even maintain my body balance and definitely slows dow the speed of work. I don’t know why these conclusions are comming so late.

February 15, 2013 at 3:25 pm
(2) Heather says:

Wondering if it has to do with impaired sleep.

I did a lot of door-slamming early on.

February 15, 2013 at 3:54 pm
(3) melissa says:

Yes, I had an EMG showing cubital tunnel in both arms. I cannot crochet, write, use scissors without fingers locking up now. Door knobs, zippers and buttons are being rather irritating to me as well. If I can hold on to my keys without dropping them it is difficult maneuvering it in the lock as well, then I gotta turn the knob too??? AAAUUUGGGHHH!!! That is the frustration I have been dealing with for at least a decade now. I was diagnosed with fibro in 2006…getting worse

February 15, 2013 at 3:57 pm
(4) Dawn says:

Yes I almost always have problems with my hands. It’s always the worst in the winter though. I don’t have enough hand strength to open cans, bottles, jars or even the plastic bags that food comes in. I also have trouble with turning pages of paper, picking things up and holding onto things. Door keys for the house of my vehicle are also tough to manipulate.

I don’t suffer from too much pain in my arms and hands. Most of my pain from my fibro starts at the tail bone and goes up to neck and down to toes.

February 15, 2013 at 3:57 pm
(5) vfm says:

hard to crochet. my hands hurt and feel numb. Always dropping things. Hate unlocking doors.

February 15, 2013 at 4:53 pm
(6) Helena says:

Yep. Over the many years, the fine motor skills of my fingers have pretty much gone on vacation, my hands and fingers cramp up easily, and I drop things often without realizing it. I’m forever losing my shopping list in the grocery store. I think I’m holding it, but lo and behold it’s nowhere to be found. Well, anyway, even though at one time I wanted to learn to knit and crochet (but my hands won’t do it), I now just find other crafty projects that my hands can manage. It’s sure interesting to learn that others with fibro have this situation. I didn’t realize it. Fascinating!

February 15, 2013 at 4:58 pm
(7) Kelly says:

OMG, so glad it’s not just me. There has been a huge increase in the number of things and times a day I drop things. I am a constant fumbler. At first it was amusing that I’d send items sailing across the room without meaning to; now its just scary.

February 15, 2013 at 5:12 pm
(8) Sue says:

You betcha! My fine motor skills are deteroating more every year since being diagnoised in 2005. Dropped keys, dropping water glass, tripping up or down the stairsor tripping over a piece of nothing on the floor; bending over to pick something up and not getting it until the 4th or 5th try. Having to use a magnifying glass to thread that needle, rereading a paragraph in a book over and over again…. I used to draw horses. I can’t now. Been making jewelry to replace that hobby and to make some money but putting pieces together gets harder especially when I am tired. And it frightens me that this will get worse as time goes on. .. If I can;t do for myself or others down the road then.what?……

February 15, 2013 at 5:23 pm
(9) Linda says:

I’ve had Fibro for many, many years and during this time I’ve found that I’m loosing my fine motor skills. Always dropping keys, dishes, books, and just about anything else I try to pick up or try to carry; some days I can pick up /carry stuff but there are more not able to days. Zippers, buttons,door knobs, threading a needle and all things like this I find very difficult. Also find that I am having problems with balance. There are so many things that I find hard to do now.

February 15, 2013 at 5:25 pm
(10) Cynthia says:

I just thought I was a klutz!

February 15, 2013 at 5:39 pm
(11) Debbie says:

I have always associated dropping things with the Fibromyalgia – I just didn’t know what the reason was! I’m very relieved to find I’m not the only person experiencing this.

February 15, 2013 at 5:48 pm
(12) messdog says:

Glad to know I’m not a klutz or by myself too. I 1st noticed my fingers & hands would make a sudden jerk or wouldn’t bend/hit or go in the direction intended. Reading & writing have became major undertakings. Until Drs. enabled me to sleep a little & prescribe a few meds I lost my ability to sign my name & then to write/type. I still have issues as with this, I’m re-writing multiple times. I was very accomplished in the culinary arts & have through the last few years lost many of my skills. I can’t judge distance or control my hands & others including family do not understand. A niece asked me to do an ice sculpture for her wedding & my sister didn’t understand my declining to do so. I drop things, can’t separate pages in the paper, I drop things or misjudge distance dropping things thinking I’m putting then on a table. I can go on & on. I no longer drive etc.

February 15, 2013 at 6:11 pm
(13) Lynn Russell says:

Absolutely! In fact, one of my first symptoms, which I didn’t realize till I was looking back, was hand dysfunction. I started dropping small items without even realizing I had done it.

I now find that I have trouble with fine motor skills, hand/eye coordination, balance and “navigation.” If I’m walking through a smaller space, or a room with lots of furniture, I’ll often bump into something because I couldn’t tell if I was centered in the open space. My hips and knees are always bruised these days! :-)

February 15, 2013 at 6:13 pm
(14) Teri says:

I am not happy to hear of everyone’s difficulties however it is reassuring to realize it is not just me!! I have pins and needles in my hands and arms and also in my feet and legs. Lately when I turn my neck in one direction I have the same sensation in a certain part of my head. I dont know if that contributes to the inability to do certain things.
Thankyou for this newsletter .It gives me hope that we are moving closer to an understanding of this disease and perhaps a cure.

February 15, 2013 at 6:58 pm
(15) Sandy F says:

Yes I also have problems writing,sewing, my biggest problem is preparing vegetables I try to peal a potato and my whole hand locks and is very painful. . I enjoy doing craft work but I have had to put it aside till a good day . Yes I agree defiantly getting worse.

February 15, 2013 at 7:25 pm
(16) Shannon says:

I broke my right pinky finger while playing softball in the late 90′s. I had to learn to write and type all over again. I still have problems with strength in that hand and can’t even close my hand around change without great difficulty. I can write about a page’s worth of manual writing. After that, it’s worse than a doctor’s chicken scratch lol!

After being diagnosed with Fibro, my hand skills deteriorated even more. I drop things all the time. It’s gotten so bad that my husband knows to come see what I dropped and if I need help as soon as that familiar noise of my cursing gets his attention haha.

It’s very frustrating when you lose control of your body like this. Worse when you know it’s permanent and only likely to get worse over time. Yet you have no choice but to roll over and give up, or decide to get on with life. I’m still kicking, and though I may drop more things than not, I still keep at it – fiercely trying to keep my independence as much as possible for as long as possible.

Not saying that Fibro is a degenerative condition. Just that lack of co-ordination seems to be yet another of so many symptoms.

February 15, 2013 at 7:26 pm
(17) C says:

I have trouble with this especially if it is repetitious. I’ve scored lower on some tests. I know there are patches on certain areas of my brain and it has coincided with some of my disability. Yet, it is not severe enough to be diagnosed as anything other than a little worse than a normal person. I also have trouble with sequencing in some ways. I do find that certain things help me exercise my fine motor skills and certain areas of my brain. I like incorporating fun things into my treatment plan like puzzles or computer games. One thing I’ve definitely have noticed is that more tired I am, the more difficulty I have even with my emotions. I’m just so down right exhausted it’s hard to function at all.

February 15, 2013 at 7:28 pm
(18) Diane says:

Yep, all of the above. I knew it had to do with the Fibro because it all happened at the same time. My handwriting used to be so beautiful, people would compliment me on it always. Now, on a good day it looks like a doctors signature or perscription. Awful!

February 15, 2013 at 7:59 pm
(19) Budie says:

I also have osteoarthritis in my cervical area which makes this problem worse. I can’t hang on to things and more tired I get the worse the problem is. A lot of times I can’t even turn on the knob on a lite switch, I really struggle open zip lock bags. One thing I want to mention here is that in reading the book by Mary Shomon “Living Well With Hypothyroidism”; she says that many people with fibro and chronic fatigue also have a thyroid problem. Some of the symptoms are so similar I was amazed. I am hypothyroid and have celiac disease along with fibro and probably chronic fatigue I learned that these can all be related.

February 15, 2013 at 8:00 pm
(20) VLH says:

I was asking my rheumatologist about this at my last visit. He mentioned that tremors can sometimes be inherited. It’s NOT tremors…rather a different type of disconnect between brain and hands. Interestingly, I can usually type, but often have trouble with writing. Printing is easier then cursive with my signature sometimes looking like it was done by a 5 year old. I also have issues with papers falling from my fingertips repeatedly and, as others have noted, dropping things a lot. My sister also has Fibro and earned a degree in art so the hand coordination issue has been very challenging for her as well.

February 15, 2013 at 10:37 pm
(21) Nancy says:

I’ve had Fibromyalgia and CFS/ME for over 30 years. I sometimes wonder if this disease is related to MS. There seem to be a lot of the same symptoms. My FM has been progressive, for sure.

February 15, 2013 at 11:56 pm
(22) Mary T. says:

Yes, my hands are affected (actually, my feet are clumsy, too). I can’t type as well as I used to, crochet, I spill and drop things, my handwriting and printing is shot, I tend to shake when trying to do detailed work . It’s so frustrating!! It’s just one more thing I have to ‘chill out’ about……..

February 16, 2013 at 1:18 am
(23) Bec says:

Have trouble with hand-eye co-ordination, used to be able to write heaps but now can’t hold the pen that long. Often drop things – its like i think i have them but they just slide out of my hand – especially if they are think (like a piece of paper). Also seem to have trouble judging things (sight) so often walk into door frames (wobbly legs don’t help). I was worried a while ago and got the optomitist to have a good check of my eyes because i felt i was getting like a blind spot but it all come back ok.

February 16, 2013 at 1:35 am
(24) Betty D. says:

I’m always bumping into things and clipping the walls. I have difficulties separating papers and as a teacher, this is frustrating.

February 16, 2013 at 10:34 am
(25) Mary O says:

I am constantly dropping things. I never know quite where things will land when I go to move them. I don’t have any fingernails due to the fact that I bash my fingers into everything and either tear them across or crach them down the middle. I never thought that it was the fibro that caused this problem due to the fact that I have always been somewhat clumsy.

February 16, 2013 at 10:53 am
(26) Mary C says:

WOW this is really an eye opener. When unable to use my fingers to hook jewlery, this before my diagnosis. I was had had Fibro since 2008 but symptons started much earlier. Looks like I have had this much earlier than 2008. I feel it started when I experienced sever migraine in 2005.

February 16, 2013 at 12:16 pm
(27) Frances says:

I was diagnosed 20 years ago but I know I had it much earlier. This was when they thought it was an autoimmune disease. Now, they know it is the way the brain processes pain. Unfortunately, they have not found the right type of medicine to help us. I was always a clumsy child and barely got through doorways without hitting myself. In the last few years, my balance has gotten so bad that I was sent to a neurologist who ran tests. I almost have no balance on my left side. This causes me to fall, stumble, and must make others think I am drunk when I take my little dog outside. My symptoms have gotten progressively worse over the last 10 years and now I have to be very careful. I sister has a two door car and I nearly hurt myself badly getting out from the backseat. My foot caught on the seat belt and down I went. I couldn’t balance enough to get it unhooked. I am somewhat relieved to hear that it is a symptoms of fibro. I hate what this disease does to us and wish more research were being done.

February 16, 2013 at 2:49 pm
(28) Cameron says:

Reading the information supplied here really helps. I thought I had just got really clumsy. My partner calls me crash cameron as I am always knocking into things, dropping things and when I go to pick them up losing my balance but he helps me retain my sense of humour about it all. I am always covered in bruises, cuts and grazes.

I have lived with FM for 12 years and just wish there was more information and more research about the progressive nature of this disease.

February 16, 2013 at 2:57 pm
(29) Nancirose Halse says:

I was diagnosed in 1988 when finding info and expectations were hard to find.
I have to second nearly every comment above. I cannot judge precisely what effects result from fibro. I was i diagnosedwith RA and also have post operative spinal stenosis, a spinal fusion, and lumbar osteoarthritis.
Idoknowthat fibro is behind my inability to fasten jewelry, watches and causes difficultydressing. I needto swim but changing clothesis a trial — fastening and unfastening bra hooks, buttons,and removinghorrible wet bathing suits.
My worst pro lem is dealing with constant pain, arms breasts ribs and torso, and feet. I would livewith everything else if I could reducepain.

February 17, 2013 at 8:46 am
(30) Sharon Fitch says:

Yes I have a terrible time some days. At work they call me klutz klutz. I bump into things all the time. Sum times it will take me two or three times to pick up something. They love me so much at work. I am entertainment for my co workers. But they all tease me in good taste. They make me laugh and keep me going. I look forward to work some days just for that reason.

February 17, 2013 at 10:24 am
(31) Maria says:

I have had CFIDS since 1995; as far as I know I do not have FM. My CFIDS/FM friends all agree that hand coordination, judgment about spatial things, etc is a big problem. I routinely knock over glasses (why are they always full of iced tea?); bump into furniture and corners so that I always have bruises and scrapes; have cuts on my hands from cooking, opening mail, and who knows what; have fallen partway down an iron staircase twice, awful handwriting, etc. I try to cope with these things by using pretty plastic glasses; having lots of paper towels around the house; putting up those foam “bumper” things on my furniture; put non-skid strips on the full length of each stair; and typing my letters (endless corrections). My hands shake, probably from the meds, but I don’t know for sure; and, oh yes, putting on earrings means I will almost always drop one of the backs and have to go searching for it on the floor.

February 17, 2013 at 2:32 pm
(32) Auntie says:

Yes, it seems to be more prevalent than anyone would think. I drop things, can’t open plastic trash bags and have poor balance. My husband keeps showing me how to open a trash bag. I know how but my hands won’t do it. I drop anything small, earrings,bracelets, rings you name it. I usually have a black and blue somewhere on my body. I misjudge the door frame and walk into a wall. When trying to leave a stadium I can’t walk in front of someone seated. I have to sit near the aisle so I don’t have to walk in front of anyone. I can just envision falling down the whole set of bleechers. I remember having trouble threading needles as young as my teen years.

February 17, 2013 at 3:45 pm
(33) Tina says:

Ditto for the clumsiness and dropping items, closing zip lock bags is a big challenge, threading needles for sure is a time consuming event and after having been a hiker for 20 years I now trip on my own feet or nothing at all. I agree with the thought that fibromyalgia and MS are kissing cousins and for my assessment you can include Parkinsons. So we can all trip the light fantastic together I guess. Tina

February 17, 2013 at 4:33 pm
(34) Rykersnana says:

Lynn – Your comments are ME. I bump into so many things. Over the past several years I just couldn’t figure out what was happening. I was bruised everywhere. I, too, am klutzy with small motor skills. I suppose that I just hadn’t looked deep enough into Fibromyalgia. I didn’t realize that was on our monster list…..grrrrrr!

February 17, 2013 at 8:41 pm
(35) Kim-A-Kazi says:

ARE U Kidding me?? I have more burns & scars from slicing open my hands, I have on several occasions have has drinking glasses & thick ones explode in my hand as I was washing them because my hands are numb so I must squeeze too tightly..One cut thru my hand on the knuckle a deep into the bone..I can not even tweeze my eyebrows my hands cramp & hurt I drop everything!! I can not tell you All how many times a day I drop the remote control!! My poor cat used to lay on the floor under where I was sitting on the couch…not any more -LOL I dropped the remote on her too many times (poor baby) I am not going to bore you with all the examples but it is partly due to the carpel tunnel I have in both hands… My biggest complaint is what is going on with my brain – we all have memory trouble = I have trouble knowing the date – year and now enunciating words./// I say topaote in stead of potatoe and I can no longer spell ( I just had to type Spell 3 times – speal speall speel – As a writer this is frightening…as a person I sound like a moorn now when I speak messing up everything stammering… that isa scary to me

February 17, 2013 at 11:53 pm
(36) Lori Rogers says:

In the past year I have lost lot of the dexterity in both my hands. I have done bead work as a hobby for many years. Now I’m afraid to even try doing it. Just the thought of it makes me depressed, which most of the time causes flair ups. The beginnings of a viscous cycle.

February 18, 2013 at 11:26 am
(37) Maria says:

Wow! I feel so much better knowing it isn’t just me having these issues. I’ve been clumsy my entire life…there were so many trips to the ER that the doctors started to think I was an abused child. (I wasn’t)

Over the last 3 years it has gotten much worse though. I too have numerous bruises & scars from walking into furniture, cutting myself while cooking or burning myself while adding wood to our stove. The tremors, stiffness & swelling get so bad that I can’t hold on to anything thin or small…especially my meds!

The doctors tried to tell me that these symptoms were side effects of the meds but, the symptoms existed before I started taking the meds. Even after they changed me to a different drug, the symptoms remain.

My boyfriend & son tease me from time to time about being so uncoordinated & even I admit that sometimes it is funny. Unfortunately, more often than not, it is more frightening & heartbreaking to feel myself losing abilities that I once took for granted. I’m not ready to give up yet though so, I just keep finding ways to adapt where possible & ask for help when I need it.

February 18, 2013 at 12:34 pm
(38) Catherine says:

Good to know. I thought I was just being a “squirell”. Not being able to keep focus and on to another thought before completing one. I drop papers all the time.

February 18, 2013 at 4:29 pm
(39) Michelle says:

I have had FM and CFS/ME for many years, though I have noticed that balance, fine motor control and eye/hand coordination have progressively worsened, especially in the last 3 years. Like many, I frequently bump into walls or door frames, knock over glasses and other items, and bump into things that I have not seen (like chairs, low tables, etc.). The worst part is falling, especially when I fall forward and hit my head and face–this has occurred at least 4 times within the last year. I fell 3 times within a matter of days–once on the kitchen tile, then on hardwood, and then on Italian tile (the hard stuff), so I had bruises on top of my already black eye. I teased that “aubergine” (dark purple) was the latest black! ^) One thing that I have noticed is that the condition worsens under extreme stress and lack of restful sleep due to severe pain. I have taken steps to reduce stress and to improve my ability to handle stress, and I avoid bending or reaching up as much as possible. Of course I say this as I sport a nasty bruise on my right shoulder and upper arm from hitting a door frame on the way to the toilet earlier this week!

February 19, 2013 at 11:58 am
(40) Linda Horncastle says:

I agree lack of dopamine could play a part but I think there are other contributing factors. Such as muscle strength, fatigue and proprioception particularly in the neck region. We had a great talk by a physio on this recently in our support group. That tight muscles in our neck can affect our balance. 7 years ago I was severely disabled and bumping into everything, unable to chop vegetables and spilling drinks. I now realise it wasn’t just the FM but the fact my muscles had weakened so much. Though I know the fatigue caused the lack of ability to exercise. I’m now much better thanks to pacing and the Alpha-Stim. The Alpha-Stim has improved my concentration and energy levels. So now I’m able to walk and swim further and therefore my muscles are stronger. The Alpha-Stim is also known to help those with ADHD (were concentration is also a problem), so there could be an element of increase in dopamine levels?

February 21, 2013 at 2:43 pm
(41) Dawne says:

At a minimum- 80% of everyday, I have extreme pain in my hands and fingers (feet also, just not as often). They ache/throb like a headache- involuntarily. Also, if I put on hand lotion and press too hard while applying, I have sharp pain. I’m even afraid to shake hands because it hurts. At times, the ache moves into my lower arms and is even more miserable when both hands and arms hurt. I was diagnosed with fibro more than 10 years ago. Just recently I completed a 10 week Fibro program through a pain clinic. I don’t see a lot of fibro patients complain of this type of pain/aches in the HANDS. Is this common, uncommon or possibly not related to fibro???

February 22, 2013 at 3:32 pm
(42) Sherry says:

My doctor told me early on to get a small rubber ball and squeeze it many times a day , while watching tv or sitting at a desk. I do this every day and it has helped some.

February 22, 2013 at 4:16 pm
(43) Pat says:

Wow funny you mentioned coordination and motor skills. I’ve always been on the clumsy side since childhood, but I still played hard in sports and other activities. Now that I’m much older I’ve noticed that my coordination is really off. I run into walls, stagger for no reason, fallen a few times, and bump into things all the time. I have so many bruises. My sons look at me as if I’m old and feeble…:) I remind them that there is a cast iron skillet in the kitchen cabinet (joking).
I have a lot of ringing in my ears and I thought maybe there were some inner ear problems. I know it’s common for us to have this problem.
I started drinking distilled water, not tap, filtered, purified, spring..DISTILLED WATER. My sister met someone in Italy who was told by her doctor to drink distilled water because of the metals and other unhealthy additives or sediments in tap water. The ringing in my ears have improved, but I still run into things. My pain level has decreased enough that most days I’m able to get out of bed. On a scale of 1-10 I hover around 4-6. To some that may be good or bad, but for me I can at least function with simple task for short periods of time. I’m not suggesting the water did the trick, but there’s so much about this condition that isn’t understood. Therefore if we can do simple things that may help….then why not?
I truly appreciate this website. Thank you so so so much!

Pat

February 22, 2013 at 5:18 pm
(44) eaglehaslanded says:

ALL of the above… & add that I dropped MYSELF 3 years ago resulting in 2 fractures of my lower right leg. I guess you could say I’ve been “lucky”-??
as I’ve had some pretty nasty falls & near falls in the past 20 odd years since I was diagnosed with Fibro. & cfs. but that was my first,&,hopefully last break!

UGH! (((hugs))) from eaglehaslanded

February 22, 2013 at 6:28 pm
(45) Nancy says:

Do those of you who experience impaired coordination have the problem constantly? I occasionally drop things and fumble, but not all the time and not always with the same tasks. Does this problem come and go, as so many FMS symptoms do? A while ago I was so concerned about this occasional problem that my MD ordered a brain MRI which was normal for my age–almost 69.

Nancy

February 22, 2013 at 8:36 pm
(46) C says:

Oh wow! I do so have problems in this area. It’s not unusual for me to fall easier, burn myself when cooking, clanking dishes, etc. I even have vertigo. I think this can at times be a separate issue but it adds to the mix. I’ve broken sets of dishes and casserole dishes and it’s been not only painful but expensive.

February 22, 2013 at 8:50 pm
(47) C says:

Replying to Nancy: For some things they are constantly there but not near as noticeable unless I’m doing the same task for a while or repeatedly throughout the day. …when I”m tired they are there to an extreme and I have to really focus my brain on what I am doing. I have to watch when bathing and use a stool and avoid doing certain tasks etc. I get use to reading my body and knowing when I should and shouldn’t do things. I hope this helps.

February 22, 2013 at 9:07 pm
(48) Lynda says:

I am a musician. I’ve had fibro for years. About 7 years ago I went into a major flare. I have come “back” some but not a lot. One of the areas impacted for me is rhythm and the beat. I can’t play like I used to. The ability to play has slowly gotten better but no where near the level I used to play at.

I also play everything slower than I used to. This has been very impacting to my soul as I love to make music.. So now, I just play it however it comes out. Off beat be dammed! :-)

February 23, 2013 at 1:47 am
(49) holly says:

I’ve noticed, especially when overly tired and stressed, that my braun and body just dont seem to be in sync. I can have a time when my brain knows I am going to falk, but it is like i can’t think through what I need to do to move my legs. I looked up Ataxia and Cerebral Ataxia. These seem to describe it well. Does this sound familiar?

February 23, 2013 at 2:36 am
(50) April says:

yes that fits me too! I can hardly write now. I’ve been trying to keep a pain journal to help me with my SSDI case but am having trouble w/ writing. I have to use tons of white out because my writing is so bad. I have to take breaks too because my hands cramp up and my fingers start to feel weird. I can’t type much either because the tips of my fingers start to feel strange.

February 23, 2013 at 10:56 am
(51) claire says:

i have had problems with this my hands seem to have a ming off their own sometimes , my hands shake all the time when i am having a bad day it increases i cant even hold a cup with out spilling it, writing is hard my hand does sporadic movements , on days were the shaking is very bad i wont go out people notice it and i hate having to try and explain it , the drs cant even tell me why it happens this had been this way for me for more than 20 years has gotten worse as i have3 gotten older.

February 23, 2013 at 11:11 am
(52) Shakota says:

I notice that I’ll drop my keys if I don’t concentrate on holding them. I have Fibro with CFS.

Also, I’m not able to push a button with the force it requires to turn the button on, the elevator, the TV, etc. There is a lot of disconnect.

February 24, 2013 at 12:47 pm
(53) Mardi says:

Glad you mentioned this — I thought my shaky hands and lack of coordination were due to changes in medications. More likely it is all part of the bigger fibro picture. Also seems to be getting worse as I age.

February 25, 2013 at 12:21 pm
(54) Georgia says:

Coordination became an obvious problem for me as my fibro. Progressed. I seem to have both large and fine muscle involvement. I too drop things and sometimes buttons are a hassle . Large motor involvement is evidenced by no longer being able to ride a mountain bike and then my road bike. Now walks of any distance seem too hard.
Georgia

February 25, 2013 at 12:35 pm
(55) Julie` says:

WOW! There are so many of us Fibromites with this same issue. There must be something to it. I thought I was just getting klutzy in my old age but now I realize it is yet another symptom that stems from FM.

February 26, 2013 at 9:14 pm
(56) julie says:

What about shakiness? My hands and fingers do cramp, but I also find that my hands are very shakey. Its embarrassing, I feel like my nerves are shot!

February 26, 2013 at 10:21 pm
(57) Melanie Collins Pennock says:

Since my diagnosis in 1999, I have been losing control over my hand function. I drop things often. My fingers always feel slightly swollen and I cannot bend my knuckles that well, which makes it hard to do the sewing and embroidery I used to do. It is hard to pick up coins. I always are afraid people do not believe me!

February 27, 2013 at 12:40 am
(58) Sherian says:

I can’t use my hands to talk anymore because I end up ticking my finger on anything on a counter or table and it flies off the counter or table and breaks. I also don’t seem to be able to walk past a chair without kicking it with one of my feet. I have nerve damage in my left foot because I have hit it so many times. It gets old..believe me!

March 5, 2013 at 9:56 pm
(59) Lyn says:

I had a total hysterectomy at 38. My pain and other symptoms came on gradually. I am not the same person I was before Fibromyalgia. I believe that menopause does have something to do with Fibro.

March 8, 2013 at 1:01 am
(60) Gloria says:

I can certainly relate to many of the comments here! In the past I was assessed by an computerized machine with regard to balance (ie to find the cause) — they never did find the cause, but I believe that it was because my thyroid levels were much too low for me.
My body cannot make adequate TSH to stimulate my thyroid to make optimal levels of thyroid hormone so I am on replacement. WHEN I keep my Free T4 & T3 levels close to the top, my balance problems are negligible. My muscles also have MORE strength.
I have large hands and fingers and have found for a long time that I am clumsy with fine motor skills and my typing can be “dyslexic” when my thyroid levels slump. Luckily that doesn’t affect my knitting and and crocheting ability, since I like to do those crafts. I am also lucky not to have too much pain — having high optimal levels of Vitamin D and thyroid hormone helps in that area. I am also taking a tryptophan prescription to keep my serotonin up and I believe that helps with the pain as well.

March 10, 2013 at 10:14 pm
(61) Benia says:

As I like to say, it’s not a day until I drop something. I usually drop something in the morning while getting ready for work. I also get hand cramps while writing in my journal. Each entry looks nice to start, then it gets all wild as I start rushing to finish writing the entry. Plus, I get shaky hands after using them for a few minutes. I noticed it after carrying something for a few minutes, or driving. The tremor is visibly severe right after and it makes it hard to eat with utensils our drink from a glass.

June 25, 2013 at 7:55 am
(62) Lorraine says:

I have had familial tremors for most of my life. I was diagnosed with fibromyalgia 10 years ago. The symptoms have been worsening. Balance, pain, foggy brain and the tremors have worsened noticeably.
There have been days when tremors affect even my ability to walk because of worsening balance and feelings of having tremors in entire body.
We have been on a big search to give me relief in back pain. Physical therapy, testing spinal injections – physiatrist does not believe in using narcotics (Yeah!!)
I am now 61 and don’t really see anytime I won’t deal with these symptoms. And I can’t see life without tremors.

November 5, 2013 at 11:27 am
(63) Cindy says:

I am SO relieved to find you all! I have been dropping things for some time now and it is worsening. I also walk into door jambs all the time..it is like I cannot judge where my body is at times. My fingers ache all day long and I have severe pain in neck, shoulders, hips and knees. but I also have osteoarthritis and spinal spondylothysesis (broke my back as a child while on massive cortisone doses for asthma) and it never healed.
I also have a terrible time opening jars or bottles.
I wonder if the menopause and/or hysterectomy may have something to do with it. i had to have a hysterectomy at age 26. I had ten years of supplemental hormones, but when i went off those the fibro really kicked in. I am so relieved to find I am not alone!

November 12, 2013 at 12:22 am
(64) Cori says:

I have several mental disorders including ADD and severe depression and am a complete clutz. Not only do I drop everything almost without realize it’s happening, almost like I entered a time warp, the object jumping out of my hands faster in time then the rest of my brain, but I trip over a single piece on the floor, continually hit my arms or leg by not clearing a wall or other object, miss my mouth when drinking and dumping liquid all over my shirt like I’m completely not syched between my mouth and hand. I’ve been told to just pay attention to what I’m doing (I also have ADD so that makes it more difficult). I went through three shirts in one day within an hour cuz I missed my mouth and spilled it). Hell I even walk into walls cuz I wasn’t looking to where I was going. But this is really getting aggravating!!

December 11, 2013 at 5:04 pm
(65) Debbie says:

Part 1 ~ Things began to get to where I couldn’t cope with the pain, I couldn’t handle a number of the “fibro” meds, and just seemed like things were getting worse. I finally came out and asked him, “How bad is this going to get…I mean, will it eventually kill me…and please, be very blunt..I just want to know”. He sat back and said, ” No, it won’t kill you, but the pain can get to the point where you’d wish it would. It could also begin to effect your movement, and if you keep going at this rate, you’ll be in a wheel chair in the next 5 years”. He was very compassionate, very understanding, and came right out and told me I had reached the point where his main concern was my comfort and pain control. Mind you, he was my primary care doctor for 15 years…I trusted him with my children and our entire family. I left him….because I felt like he had given up on me…and I wanted to find some one who would find out what was going on with me…my right foot was starting to drag.

It is now 2 years later…I’ve been being seen by a teaching hospital, have seen specialist after specialist in every department you can imagine…..and my original doctor was right. I am in a hospital bed now, not only can I no longer move my right foot, but can’t stand on or move my right leg at all…except to pivot from the hospital bed to a commode and back again. I run fever at night sometimes when its really bad, the pain is in my entire body, I too have difficulty with my hands not being as “reliable” as they once were….very clumsy, and I have what I call short term memory loss but the doctor said was “fibro fog”. I have seen well over 15 or more doctors, and through out this entire experience, only 2 doctors told me “Yes, your lame leg/foot can be fibro related.”

December 11, 2013 at 5:07 pm
(66) Debbie says:

Part 2 ~ All the other doctors swore it had to be something else and I don’t even want to begin with all the painful, excruciating tests they put me through…so sure there had to be some other underlying problem. Now, 2 years later, they’ve all dismissed me because they said they have no idea what’s wrong with me, but one thing they do know is that this is not from fibro. I have news for you…it is. The weather effects it, stress effects it the position I’m in effects it…my fibro is excruciatingly painful, and because of my inability to handle the pain sometimes, I end up in the hospital just for “pain control” to get me back to my base line pain level….the last time, it took them 8 days to get the pain level back down. My “normal” pain meds are Oxycontine, Percoet, Valium, and Soma…. and with all that, I still need “pain control” from the hospital every so often. Don’t let anyone tell you it can’t do this to you. I have all my test results, blood works, MRI’s, CT scans, EEG’s..you name it…and my blood work shows that the more I try to move around or exert, my inflammation levels sore sky high and I can’t move at all….anywhere…my shoulders, my arms…even moving my head from side to side. The blood work shows it. So there will come a time when the fibro gets to the point that exercise is NOT recommended as it will only make it worse. The lesson I learned from 2 years at a teaching hospital with numerous specialists in this field? I’m going back to my primary care doctor who had compassion, understanding, and predicted exactly what has happened to me. Why doctors can’t just say, “In some severe cases…….” and then express what is known as fact…as they now see in my case, but have dismissed me and are now trying to farm me out to another University hospital for “fresh new eyes” to examine and maybe they can find something. My primary care doctor found it years ago..

December 19, 2013 at 3:11 am
(67) baarbara says:

I had fibro for ten years, after I had lyme..disabled in bed..then got off pain killers..ocycontin 90 mg a day and went back to work, lost weight and functioned…now ironically, I don’t have fibro pain at all for fifteen years now, but have recently been dropping object like crazy and breaking glasses all the time, misjudging placement of objects and their falling and just plain clumsiness…some off balance stuff too.

anyone else out there?

Barbara

January 8, 2014 at 10:06 pm
(68) Bobbie4201 says:

I can’t tell you all how much this website means to me. I, too, have been having problems with coordination and balance. Have had FB for 10 yrs. I dropped things, knock over glasses, stumble over nothing and have had 2 bad falls in the past 2 months (the latest 2 days ago). Until I read all of these comments, I didn’t realize that FB could be the cause of my problems. I used to play golf, ride bikes, etc. but am unable to now. Very depressing.

January 10, 2014 at 10:44 am
(69) Andrea says:

I’ve noticed a marked increase in my difficulties with my hands and my general coordinationwithin the past year.

January 16, 2014 at 6:28 am
(70) Vinod says:

Once i want to just lift umbrella to threaten my boxer dog and it all of a sudden lost control of my right hand and hit myself on the eyebrow. I was bit scared and could not believe what has happened. After couple of months i went to a vegetable shop and try to check a coconut if it has water in it. I remember just picking it up and it again lost control and hit on my eyebrow again.

Doctors suggest me to take levipil 500mg two times and in a day i can feel couple of times my hand shakes by itself and some time does not respond to me properly.

January 21, 2014 at 8:43 am
(71) Cathy says:

I have these problems but don’t know if the cause is from fibromyalgia or even carpal tunnel syndrome. Also have problem picking up coins from cash drawer at work. My fingers look almost arthritic when I try this.

January 26, 2014 at 2:03 pm
(72) Roxie says:

Wow its not just me. So glad to know this. Its worse the more tired I am. Fine motor skills are compromised. Fingers tremble and I can’t pick up small stuff like pills. I drop things a lot. Have a hard time holdind dishes to wash. Hand cramp when I write. At times my fingers tremble so bad I can’t text. All getting worse as time goes on. I’m only 48. Kind is scared as my body continues to rebel.

February 15, 2014 at 8:57 pm
(73) tracey says:

Hi, my name is Tracey, in the last year I will pick up things and my hand will just drop them in mid use. I have broken many items and have whittled my waist with continual picking up of other items. It is getting worse and starting to scare me. Anyone else with these issues?

February 18, 2014 at 2:13 am
(74) opbatra says:

I am 56 yrs old ( I am a patient of High BP- 90/155 last 20 yrs- I am taking regular medicine Amodip-AT half tab. ,Half Tab. Dizral Plan and Multivitamin Cap. ,daily after breakfast ) I play table Tennis Game,daily walk and I am doing job ) I feel cramps in only right hand during taking tea,shaving , writing and I feel more cramps after playing,nervousness, computerwork

February 18, 2014 at 9:36 pm
(75) Hollie says:

Have not been told I have it but god does all this stuff fit me to a T. My fine motor skills are getting bad I’m a server I find that if I’m carrying something in my hand like a pitcher my hand actually freezes in that position and it hurts so bad and there is nothing I can do till it unfreezes does anyone else suffer from this? My balance seems to be getting real bad wondering if it’s all connected

February 20, 2014 at 6:17 pm
(76) Wendi says:

I have this problem and fibromyalgia. It actually has caused me an enormous amount of anger that is hard to control. I mean really, how can you not get angry when you constantly drop things, knock stuff over ,ect. I will literally get to a point where I am so fed up I will just throw whatever it is I can’t hold on to. It is just not fair to be 33 years old and have the coordination of a toddler. It is so humiliating to be in public and trip over the big fat nothing on the floor or spill your drink in a restaurant. I can’t even date because of it!!!! I have so much anger and frustration built up due to chronic pain and clumsiness stealing my life away. It just isn’t fair.

February 22, 2014 at 12:18 pm
(77) Saroj says:

I was diagnosed in 2003 after 10 years of symptoms. Not being a clumsy person, I dropped dishes, cut myself when cooking and even forgot where to store dishes.

March 26, 2014 at 11:29 am
(78) Castle Clash Astuce says:

nuttily  nutting  nutwood  nuzzled  nuzzler  nuzzles  nylghai
 nylghau. sneezed  sneezer  sneezes  snelled  sneller  snibbed  snicked  snicker.
toney    tonga    tongs    tonic    tonne    tonus    tools    toons.

Also visit my web-site :: <a href=”http://www.blogdigger.com/add.jsp?rss=http%3A%2F%2Fppir.at%2Fcastleclashforandroiddownload805244″>Castle Clash Astuce</a>

April 10, 2014 at 6:11 pm
(79) Gracie says:

I have a poor sense of balance and coordination plus vertigo at times. I find that my brain reverses many things like left and right. My speech is very much affected and I find that I have the right word in my head for the sentence but I say something different, usually related but not right. I used to have a great sense of direction and found on a long trip when we weren’t using the GPS hubby used to ask me the way and I used to be spot on and now with the fibro I am most often wrong.

When I walk I am not balanced and I tend to veer of to one side. I am clumsy and have taken some falls and many near falls.

Does this sound familiar?

Leave a Comment

Line and paragraph breaks are automatic. Some HTML allowed: <a href="" title="">, <b>, <i>, <strike>

©2014 About.com. All rights reserved.

We comply with the HONcode standard
for trustworthy health
information: verify here.