Constant excruciating leg cramps
I was “diagnosed” with Fibro in 2009. I had a false pos for Lupus and so this is what they decided I have.
My symptoms increased and decreased in severity for years. About 11 years ago I started getting leg cramps in my sleep. Sure, everyone gets them, but mine would be calf and shin simultaneously. I couldn’t stretch one or the other, because the opposite would spasm more and cause terrible pain. I’d have it for a couple weeks and then it’d disappear.
I went through times were I was very active, in the gym all the time, hiking, etc. but then I’d get, say, tendinitis somewhere and have to lay off.
In august 2021 I fell. I’d been exercising and walking—up to 4 miles a day— for a couple months. I didn’t fall because of pain or disability, I just tripped in a normal way. But I landed in my face requiring stitches in three places, and got whiplash.
Since then, I’ve been downhill. But the cramps! I started getting them in both legs at night. Both shins, both calves, the feet. It decreases in intensity, but hasn’t gone away. Then it increases again. It used to stop when I was up and around, but now both legs are pretty much in spasm all day. It spread to my hamstrings (never as bad), and now I have it in my forearms.
The rheumatologist found “nothing wrong”. The neurologist found “nothing wrong”. He put me on gabapentin, but anything more than 300mg once a day turns me into an a$$h*le. And doesn’t help.
The doctors literally wipe their hands and say, “that’s just your Fibro.”
Is it? I’ve never read about that with Fibro. 🙁
56 yo. Used to bodybuild. Played women’s pro football 20 years ago. Used to cycle, swim, etc.
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Hello @lfisher66. You played woman's pro football for 20 years!?! That's incredibly awesome. Scared of you! Indeed you were active and a go getter from the sound of it. I used to be too, in a different way, but I get it. I'm 52 and my overachieving, go getter A -Life days are gone. Unfortunately, I lived my horrid B-Life for about 6 years...ya know, kind of like you're living now, unstable, chronic symptoms, deconditioning, sensitivities, a merry go round of meds and side effects, depression, anxiety, stress, and doctors having no plan of action.
Long story short, for the past 1.5 years I've been discovering my C-Life which has taken a lot of hard work, refocusing, regrouping, recommitting and shifting gears to a much more stable, moderate and flexible path forward. Yes, I still live in chronic pain, but I'm more equipped to manage it and find that life can be more than the B-Life. There is hope, you've just got to find it.
After reading your posts, I learned that you are stuck in a terrible cycle of doctors going in circles and not being able to give you better answers other than,"it's your fibro", or "will the pain away". I know how much that hurts the soul when you're suffering and practically begging for more answers or help. Regarding the purpose of your new thread...have you tried muscle relaxers for your awful cramps? How about gentle daily stretching? As much as it hurts, keeping your body moving is the best thing you can do. Do you mind me asking how you're dealing with your emotional trauma and depression?
So much of your situation speaks to me and I think it would really be worth your while to check out this video by Mayo Clinic's Dr. Sletten. He presents on Central Sensitization Syndrome (CSS) which explains how the central nervous system can wind up causing an upregulation, resulting in popcorning chronic pain and symptoms.
Here's the video:
Please keep in mind when watching that CSS covers a lot of territory and not every single bit applies to each person. Watch with an open mind and please let me know if you think CSS may answer your frustrations of "what" and "why", especially when your doctors can't.
Lastly, I want you to know that I believe in you and think you certainly possess perseverance and discipline as proven by your past A-Life. That tells me you've got what it takes to get yourself through this not so pleasant, challenging B-Life, and work your way towards a more productive, stable C-Life. You just need help and a plan. Please let me know your thoughts on what Dr. Sletten has to say about central sensitization. Do you think any of it applies to you? Do you have questions for me abut my journey with CSS?
Haha! Lord no! Twenty years AGO! Haha
Bahahaha! 🤣 My bad. I mis-read that.
lfisher66's symptoms sound exactly mine, but I don't have fibro. I was told to stretch more and try magnesium. Not working.
I will watch it. My doctor did refer me to the Pain Clinic. (I’m with Kaiser.)
They said, we’d like you to start CBT. Yes, I said, I’m familiar with that. Let’s give it a shot.
Well, it’s in group sessions only, oh, and virtual, and available on the two days from 10-12:30, or these two days from 3:30-6.
I say, I work from 12:30-6:30.
She says, can you work at 12:30?
1) No. 2) Nor can I magically appear somewhere immediately after finishing a virtual group.
I asked if the “Pain Clinic” also offers any Physical treatments—physical therapy, trigger point therapy, chiropractic? She says I will have to make an appointment with the clinical psychologist. They’ll let me know when that’s available. Haha.
I have tried muscle relaxers in the past. Magnesium, potassium, I do stretch— I pretty much have to. I’m currently going off the Gaba because it doesn’t help at a low dose and the Neuro doesn’t “discuss” with me (via e-message), he just tells me to take more. Not, “try taking 300mg more at night,” just “try taking more.” Grr..
Additionally, I was recently diagnosed with ADHD (formally. I’ve known for decades! Haha) That doc prescribed Wellbutrin. After about a month I messaged that I felt good on Wellbutrin, but not any different than any time feeling good Without Wellbutrin, and it Definitely did not help with ADHD symptoms.
Turns out directly after seeing me once (virtually of course,) my doctor left Kaiser. That was probably three months ago and they’re still waiting for a replacement doctor. I called and asked “Was that the Only psychiatrist in Kaiser? Can’t I just get a different doctor?” Meanwhile, they prescribed my adderall, of which I take the smallest dose once a day. It doesn’t help either, and, in fact, I suspect it makes my pain worse. After I get off the Gabapentin, I’m going to get off the adderall. (I don’t want to quit everything at once and this is literally only going to be a two week process since I take so little of each.) When I tell the docs they say, “Okay.”
Anyway, I’m rambling on now, but am interested in anyone else having these terrible, constant cramps.
Thanks all! 🙂
PS-I’m not “down and out”. The facts may suck, but it’s just what it is. 🙂
Can you tell me more about it?
My calf and shin muscles are Always in spasm, even when not “cramping”. The neurologist stuck a wire in my muscle and told me there’s nothing wrong with them. Then he told me, multiple cringey times, “you have fabulous muscles.” I said, “Look, that’s the Problem. I don’t work out, I’m not flexing. They are like that All The Time.” He just told me again they’re fabulous.
What about a muscle relaxer. I’ve started one. Not enough yet to stop the leg and foot cramps completely but not all night now.
My first symptoms of peripheral neuropathy were constant painful muscle spasms in my toes at night and extremely tight calf muscles that did not respond to physical therapy. The first diagnostic step was an EMG. My peripheral neuropathy was caused by an autoimmune reaction due to the Covid vaccine. Could you ask the neurologist if he would consider ordering an EMG?
@lfisher66 I'm glad to hear you're not down and out, and you are able to work. It's too bad you've chosen to discontinue Gabapentin so early. The name of the game is to titrate up in dose. That is what a doctor should recommend. It can be challenging to hang in there while the dose slowly increases before determining if you've found relief. Maybe you'll try again one day. Pregabalin (Lyrica) and Gabapentin are both are recommended for Fibromyalgia.
It sounds like you're doing all the right things for your muscle cramps...stretch, walk, exercise, magnesium. How about your hydration? Are you drinking enough water throughout the day? How about Epsom salt, warm baths and massage?
I found this Clevland Clinic article on muscle spasms. It might be worth a read:
https://my.clevelandclinic.org/health/diseases/15466-muscle-spasms
The only other thing I'll throw in is that all the tips and tricks for muscle cramping can be used, is that the addition of learning how to strengthen your belief in your abilities to learn how to effectively deal with stressful situations is clutch. Especially living with chronic conditions like fibromyalgia. You mentioned cognitive behavioral therapy (CBT). I'm sorry it's difficult for your scheduling purposes, but please don't give up on it.
@pacer3702 had a good question about EMG testing. Have you had a nerve conduction study or EMG testing to rule out other causes? I too experienced muscle cramping and twitching from neuropathy. What have your doctors ruled out?
Thank you so much for this video. I am suffering too from Chronic pain and was on reading some posts, I have just started with the leg pains and cramps and my MRI ‘s do not show issues that could cause this even though I have had multiple back surgeries. I so appreciate everyone sharing their journeys …lfisher66 I am sorry this is happening to you as well. I too was super active, Pilates , trainer, roller blading, nothing now…
Will be watching your video in a few hours at length , thank you again. I am seeing so many Doctors and no answers yet.