Costochondritis
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I notice I often get costochondritis (chest inflammation) mimicking a heart attack. Is that common with fibromyalgia? What can I do to eliminate this? It not only hurts but gets quite scary.
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kaz_40 sickntired771
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pam_87693 sickntired771
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amybober5982 sickntired771
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Wish you well I know how you feel.
cherl450 sickntired771
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katharine81627 sickntired771
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deb97936 sickntired771
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katharine81627 sickntired771
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kaz_40 katharine81627
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katharine81627 sickntired771
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kaz_40 katharine81627
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marlene_40 sickntired771
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I have been diagnosed with Costochondritis also. It was been the worst pain I have ever suffered. It started with me going to ER thinking I was having a heart attack. I suffered in pain for 7 weeks. I was given pain meds through an IV which didnt alleviate my pain so on top of IV pain meds they gave me pain pills. FInally I got relief. Soon after the pain returned I tried chiroprator and got no relief. I went to a Acupuncturist and ............... I got relief I continued to do acupuncture and massage during the 7 weeks. Got an attack 4 months later went straight to acupuncturist and got releif. I am continuing my acupuncture treatment and getting massages even though im not in pain, doing it as a preventitive measure. I dont want that pain. Its awful ;( But that is what works for me I wanted to share that with you all. I also take a magnesium supplements. I will be starting fish oil I read on here that it worked for someone. I wish you all healing in your body. Costo is painful and ugly.