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Chest Pains



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08/05/2008 00:01
joijoy1
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Hello

I am new to the lupus support group, and I would appreciate any advice anyone can provide for me. For the last eight years I have been experiencing extreme chest pains accompanied with nausea and vomiting. The episode usually lasts 24 hrs. I have been to see a cardiologist, a GI specialist, and have had a full workup on my lungs. Nothing significant was found. I am tired of going to the ER when this occurs because all they can do for me is give me pain meds. I am at my wits end because this prevents me from doing my activities of daily living. If anyone is going through this or knows a solution, please help.

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08/05/2008 11:43
momwife26
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Well I am going through that however I have yet to find out the reason for it myself. I have had all the same tests and still nothing. I have stopped going to the ER and just taking a pain killer and a phenergan and resting. I am sure that is not a good solution but it is all I have come up with. I definitely empathize with you I am going through the same things. Have you seen you rhematologist during those episodes? I may help if you go to your primary or you rhematologist when those things come up so they can chart them and also see if there are changes in your activity levels. I can't do that because of costs and my rhematologist is an hour and a half away but it may be an option for you.

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08/06/2008 20:09
Wildflowergirl
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I have gone to the ER 6 times this year for chest pain that make my arm go numb and fingers tingle.It was all Lupus pain. Unless its crushing pain and you can hardly breath and its constant pain that stays with you go to ER! If it gets worse with a deep breath in its Lupus! I too know all about this frustration its a Lupus thing.

I asked how the heck will I ever know if it's my heart for real VRS Lupus chest pain??

ER DR said this," If its crushing so bad like you can't move and feel like you have a hundred books on your chest and it wont go away and if you it dosen't make a diffrence if you take a deep breath in or out, its heart go to ER! All the other pain is lupus crap it feels like a cramp in your chest right? I know so well its so scary.i have had pain right over my heart. Numb hands tingle figers chest pain. Its so very commen in Lupus. Hang on I know its sooo frustrating! Do this, just have the DR get you a good pain killer to have on hand like Percaset for these times of great pain in your chest and anxity meds also help when this happens too because when it comes it can freak you out and make you start having an anxity attack that makes it worse more then it really feels like a heart attack.The anti anxity meds calm you down a bit make you relaxe. My primary said Lupus brings on anxity and depression (so thats why I cry so much) I so know what you go through.

THe last Er visit I had I felt like butterflys were flying around in my chest with pain it really freaked me out that was a new pain but guess what? It was the same old Lupus wacked out chest pain. GO FIGURE!

I dont even tell the Doctors office now that I have chest pain, I just say I'm in a flare, I need pain meds and should I go on prednisone? If you even mention chest pain they freak and say go straight to ER to cover their butts in case.

You just need to get like I am now and start knowing the same chest pain and signs to start feeling what the "NORM" chest pain is in a Lupus flare.

To save us money ( I own 600 in copays at ER)time and pain at the ER. Im so sick of hook me up to the EKG, "looks fine", "your fine!" and them treating me like I am nuts!" Take this shot or pill for pain." "See you later!" "Follow up with your DR."UGGG! You ever want to chat Email me wildflowerfulz@hotmail.com

Post edited by: Wildflowergirl, at: 08/07/2008 05:45



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08/07/2008 05:45
momwife26
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I get the same feelings I had a couple of irregular EKG's and a x ray that showed my heart was enlarged and they sent me to the cardiologist who basically wrote off all the pain and said you just need to loose weight and left it at that. He said you are too young to have heart trouble. Since then every time I mention it it is like they are looking at me like I am crazy and ignore what I say. I have really gotten discouraged with the physicians. Now I basically go when I know something new is happening and it needs to be documented and when I need meds. I have gotten very discouraged with the whole thing. I do worry about not knowing if I am having a heart attack or not or when my pain is serious or when it is just Lupus and nothing can be done about it it scares me to death but I am just trying to learn to live with it and pray for grace.

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08/11/2008 19:08
joijoy1
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Thank you for responding. Unfortunately, my rheumatologist does not have a solution either. She did refer me to a pain clinic to get the pain meds that I need. I guess this is my only solution, and I hate it, but I will manage. Let me know if i can help you!
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08/11/2008 19:09
joijoy1
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I am going to a pain clinic this month, so hopefully the situation will be handled. Thank you for responding
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09/08/2008 20:51
polivito
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When my chest pains first started (also about 8 years ago) my rheumatologist diagnosed it as costacondritis. I am not sure if that is it or not but I have the super-intense-hard-to-take-a-breath pain that lingers and causes pain up and down my arm. I do start to panic too and haven't considered anti anxiety meds before but I think I will talk to my doctor about it. I hate to go through life so medicated but it seems to be becoming my only way to function.
Paula



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10/21/2008 20:24
tleigh71
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If the connective tissue between the ribs and sternum become inflammed it can be very painful but not too serious....I have gone to the hospital 4 or 5 times this year with chest pains/shortness of breath. I have learned to keep my own blood pressure cuff that also measures heart rate and when those vitals are too high along with the pain then I definitely go to the ER. Hope it helps.

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11/19/2008 13:37
ColdJed
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I've also had serious pain in my chest and left arm, and though I'm young and fairly fit, I thought I was having a heart attack. I went to the ER and had an EKG (Or ECG...the stickers on the chest..I get them mixed up) and the doc told me I had Costocondroitis.

Essentially, it's an inflammation of the chest cavity which can cause severe pain and make it difficult to breathe. The doc said it's more common than most people know, and that you can get it by leaning too hard for too long on something, or doing it repetitively. As a carpenter, I'm always bending over and leaning on this and that.

Anyway, it was about three months after this incident that I was diagnosed with lupus, schleroderma, and raynauds (as well as GERD). I actually didn't know lupus could cause that kind of pain. Perhaps the doc's diagnosis of me was wrong??

-Jared

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