Does Fibro mimic heart issues?

Melissanicolle

New member
Joined
Mar 22, 2023
Messages
2
Reason
DX FIBRO
Diagnosis
06/2018
Country
US
State
PA
Hi Everyone-

I was wondering if fibro can mimic heart issues. I have times where I have pain around my chest area, as well as my neck and back. My wrists will be sore, and feel worse when I move them around. It scares me because I worry it could be heart related, but my doctor tells me my heart is fine. When I have these spells I sometimes feel hot and cold too. Just wondering if anyone else has experienced these types of symptoms.

Thanks!
 
In my experience, those symptoms could possibly be costochondritis, which is "chest" pain actually coming from the rib cage. It can be quite painful and cause alarm. It's particularly painful in the sternum and under the breasts. The back pain can be a byproduct, being that it's also part of the rib cage. And the neck is oh so close as well. It's always a relief to know it's not your heart.

I'm finding it difficult to offer to you what helps, as I've had this condition for many years and it's never fully resolved. Steroid shots failed and codeine got out of control (for me). Maybe look it up and see if what you read describes what you're feeling. Perhaps regular antiinflammatories would help you.

As far as wrist pain, I have that too, although I think it's just a fibro thing. Maybe a little arthritis. And feeling hot and cold...could that be stress related?
 
@Melissanicolle ......
Often those of us with fibromyalgia tend to attribute any new symptom to the fibro, and often that is what it is. But anything that is new, and most especially if it involved chest pain, should always be checked out thoroughly by your doctor, because if it is something else you really need to know, and know as soon as possible. Has your doctor seen you recently for this symptom? If not, you might want to go again, or even seek a second opinion and an ultrasound if you have not already had one.

Of course, there are also other things that can cause chest pain, such as anxiety and indigestion. Might be worthwhile checking into those things as well.
Wrist pain could possibly be carpal tunnel syndrome. I was diagnosed with that some years ago, but I discovered that the pain and the numbness was caused by sleeping with my wrists curled, which many people do. Once I trained myself not to sleep that way, those symptoms almost completely disappeared.
 
Thanks so much for your reply! I see my cardiologist annually for MVP, but he always assures me my heart is ok. I have an appointment scheduled for March. I've often wondered if I have carpal tunnel. I think my sleeping position could be contributing to my numbness in my hands as well. I have mentioned that to my PCP in the past, and she thinks that's what it is. I also have acid reflux too. I also have pretty severe anxiety too. It's tricky to figure out what the symptoms are coming from!
 
@Melissanicolle ...You can change how you hold your hands and wrists when you sleep, and it will make a huge difference! At least, it did for me. Now, one time when I told a doctor about this, he started laughing at me as if this were not possible. But I did it, and anyone can, I think.
When I got into bed, I would very deliberately put my hands flat on the bed or pillow, wherever, and I would repeat to myself "Hands flat, hands flat" over and over. When I woke in the night, I would again straighten out my wrists and hands and repeat it over and over until I fell asleep again. It only took a few months to break the life-long habit of sleeping with my wrists curled. And a few more months after that for all of my carpel tunnel symptoms to go away. But it worked.

Now, I still have the carpel tunnel syndrome in my wrists....doing that didn't cure it. But the difference is that I was feeling extreme pain in my wrists any time I picked up anything slightly heavy like a pot from the stove, and my hands would go numb frequently both day and night. Now, my hands almost never go numb and that pain on picking something up happens maybe a few times a year. It's been about 5 years since I retrained how I sleep and it has made all the difference.
 
This is going to ramble through a few subjects, starting with costo-chondritis, so I hope it's not too confusing. Costo-chondritis can be very painful, and if you have larger breasts, it may simmer beneath the surface most of the time once you get it. A heating pad may help a lot until it calms down. The feelings of being hot or cold for no logical reason with chills, and goosebumps can come and go, and I believe they are due to dysautonomia. POTS and NMH are also due to that, imo. If you have been diagnosed with MVP like so many of us are, and even if you haven't, reading about MVPS aka Mitral Valve Prolapse Syndrome may help you with understanding some of the strange symptoms we get, since that syndrome includes dysautonomia. I have always thought that most of our symptoms are due to dysautonomia, but that still does not tell us what originally caused the dysautonomia. My cardiologist told me I do not really have MVP because they now know that mild heart valve prolapses with mild regurgitation are normal in most people as they age. Over 30 years of being told I had MVP and was on my way to heart failure were erased because the Echocardiographic ultrasound technology has gotten so much better. A list I saw had congestive heart failure as the number two cause of death in people with FMS, so I figured that would be my eventual fate. My point here is they can make major changes even in your diagnoses as more is learned. Many of us eventually get diagnosed with chronic Lyme and I am also one of those. The cardiology P.A. told me that he believes most chronic Lyme symptoms are due to dysautonomia. An Israeli study showed whiplash injuries were responsible for 41% of Fibromyalgia cases, making it the number one trigger. The autonomic nervous system (ANS) runs all over the body, but the brain stem at the nape of the neck comes as close as you can to being the center for the autonomic nervous system, so that makes sense. It seems to me that anything that helps strengthen the parasympathetic half of the ANS should help us feel better, like vagal nerve stimulation, GABA, foods that raise serotonin, Seriphos, L-theanine, valerian, lemon balm, mindfulness, meditation, spending time in nature, and so on.
 
Hi Everyone-

I was wondering if fibro can mimic heart issues. I have times where I have pain around my chest area, as well as my neck and back. My wrists will be sore, and feel worse when I move them around. It scares me because I worry it could be heart related, but my doctor tells me my heart is fine. When I have these spells I sometimes feel hot and cold too. Just wondering if anyone else has experienced these types of symptoms.

Thanks!
Hi!I have quite a lot of discomfort around my left chest and it runs down my arms.i think I’m havin a heart attack.had cardiograms,full blood count and cholesterol all checked.all good.so it’s either fybro related or a nerve trapped.trouble with fybro u don’t know whether it’s one or the other.i can’t regulate my body temperature,recently I’ve been sweating terribly which is quite embarrassing,i stand outside with no top on in -4 just to have a bit of a cool down.neighbours will think I’m nuts😂😂fybro has riddled me for 30 years and I’m still in pain.we’re all different but mine was chronic.was on fentanyl patches and tramadol
 
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