Constant excruciating leg cramps

Posted by lfisher66 @lfisher66, Jul 16, 2022

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.

Interested in more discussions like this? Go to the Chronic Pain Support Group.

@leigh17

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.

Jump to this post

Hello @leigh17. You're very welcome! It's an eye opening video. I'll be curious to hear your take on it.

I'm very sorry that you're suffering from chronic pain. When did you first begin having symptoms?

REPLY
@rwinney

@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?

Jump to this post

I did have the EMG. I also recently had a brain MRI, to rule out the possibility of MS, even though it was at my request—the Neuro is convinced there’s nothing to indicate MS.

I actually just got the result yesterday (via the online portal that just drops info with no discussion) but I have not heard from the doctor.

This may sound funny, but I’m using my phone and I want to switch to the computer but not retype everything….

REPLY
@pacer3702

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?

Jump to this post

I've had that. He said "there's nothing wrong".

REPLY

Okay... so anyway.... the results of the MRI, from what I can decifer, are basically thus... "(the things that are indicated) could be normal from age, or it Could be (list of things, one of which is "a chronic demyelinating process...") . I already assume my doc will say it's fine. Which would be a relief if I didn't already think he's a schmuck. haha,

REPLY
@rwinney

Hello @leigh17. You're very welcome! It's an eye opening video. I'll be curious to hear your take on it.

I'm very sorry that you're suffering from chronic pain. When did you first begin having symptoms?

Jump to this post

Hello, I thought the video was very informative. I have had chronic pain since 2016 after a cervical fusion and a failed shoulder replacement, as well as back pain that is worsening. However this new pain started about 4-5 months ago and is worsening. My EMG shows possible small nerve fiber neuropathy buy the cramping in my legs is getting worse as well as my back pain. Seeing my Pain Dr as well as primary this week . My hydrocodone is only taking the edge off. I also take 2400 g of Gabapentin a day.

REPLY
@lfisher66

I've had that. He said "there's nothing wrong".

Jump to this post

Despite the nerve pain and muscle spasms, my first EMG at 5 months post vaccine was essentially normal. The EMG became abnormal at 7 months and continues to be abnormal. Autoimmune reactions take time to fully develop. Just in case this information helps you ...

REPLY
@pacer3702

Despite the nerve pain and muscle spasms, my first EMG at 5 months post vaccine was essentially normal. The EMG became abnormal at 7 months and continues to be abnormal. Autoimmune reactions take time to fully develop. Just in case this information helps you ...

Jump to this post

I appreciate the info. I did have the vax, but I had these issues before it, so I don't think it's a reaction... though, thinking about the timing, the increase in severity maybe. Hmm

REPLY

I've been having severe pain in my shins and the anterior tibialis (the muscles in the front of the leg, not the calf).

I'll make a long story short. After YEARS of physical therapy and lots of "it's probably arthritis", a recent MRI confirmed what my latest physical therapist and doctors suspected. My lower back is causing the pain.

To test this theory, I stopped putting pain relief topicals on my legs. Instead, I put it on my lower back. In a day or two, the pain was much reduced and bearable.

Do an internet search for dermatome and look at the illustrations. Find the area where your legs hurt. Mine was labeled L4-L5, which, oddly enough corresponded with what the MRI confirmed: bulging disks and facet joint arthropathy. My previous doctors were looking at the Xrays, CT scans, and MRIs for both the knees and the spine and saying, "Your arthritis isn't severe enough to cause the pain you're describing. Try Tylenol."

You might not have the same problem, but it's easy enough for you to check out (putting topical pain relievers on your lower back and seeing if that helps).

And yes, I've had the vaccine and boosters, but this pain started at least 4 or 5 years ago.

REPLY
@leigh17

Hello, I thought the video was very informative. I have had chronic pain since 2016 after a cervical fusion and a failed shoulder replacement, as well as back pain that is worsening. However this new pain started about 4-5 months ago and is worsening. My EMG shows possible small nerve fiber neuropathy buy the cramping in my legs is getting worse as well as my back pain. Seeing my Pain Dr as well as primary this week . My hydrocodone is only taking the edge off. I also take 2400 g of Gabapentin a day.

Jump to this post

Hey there @leigh17, I'm sorry to hear of your failed shoulder replacement and worsening back pain. Nerve "excitement" makes sense given all your body has been through. That's why I felt learning about central sensitization might be helpful. You check a lot of the CSS boxes.

You mention seeing your pain doctor and primary this week. Have you seen a neurologist yet? They can order a skin punch biopsy to officially test for small fiber neuropathy.

I went down the same path, taking a narcotic for pain relief, and used your very words of "hydrocodone is only taking the edge of". Please be aware opiates can induce hyperalgesia as well, so when we think they are helping for that small window of time, they can in fact induce more pain.

You have a lot going on and this all seems to have turned your life upside down over the past 6 years. I understand how important it is to get situated in diagnosis first, but I'm wondering if you've ever considered going to a pain rehabilitation program like Mayo Clinic? Not a pain doctor or pain clinic, but a program that helps you with function over feeling by preparing you physically, emotionally and behaviorally. It's different than pain management docs and places that focus on meds, injections and procedures. Just a thought.

Hang in there, my friend, and above all else keep your chin up! Good luck with your appointments this week.

REPLY

I've been having severe pain in my shins and the anterior tibialis (the muscles in the front of the leg, not the calf).

I'll make a long story short. After YEARS of physical therapy and lots of "it's probably arthritis", a recent MRI confirmed what my latest physical therapist and doctors suspected. My lower back is causing the pain.

To test this theory, I stopped putting pain relief topicals on my legs. Instead, I put it on my lower back. In a day or two, the pain was much reduced and bearable.

Do an internet search for dermatome and look at the illustrations. Find the area where your legs hurt. Mine was labeled L4-L5, which, oddly enough corresponded with what the MRI confirmed: bulging disks and facet joint arthropathy. My previous doctors were looking at the Xrays, CT scans, and MRIs and saying, "Your arthritis isn't severe enough to cause the pain you're describing. Try Tylenol."

You might not have the same problem, but it's easy enough for you to check out (putting topical pain relievers on your lower back and seeing if that helps).

And yes, I've had the vaccine and boosters, but this pain started at least 4 or 5 years ago, before COVID was a thing.

REPLY
Please sign in or register to post a reply.