Et tu, ribcage?
Mar. 11th, 2009 09:55 pm![[personal profile]](https://www.dreamwidth.org/img/silk/identity/user.png)
My chest hurts.
(No, it does not feel like heart pain.)
Someone suggested costochondritis. I don't want to think about cartilage inflammation. But it is a common syndrome attached to fibromyalgia; the majority of people with fibromyalgia will develop it. I don't think I have it. But I do need to see my doctor soon, so I will ask to be checked out.
http://www.geocities.com/lynndebeal/CostoPain.html <-- I love this webpage, it makes me smile.
NOTE: The following bit of venting is not aimed at any of you. It is aimed at me, myself, only.
Also, I am tired of this. I am tired of feeling as though I walk on eggshells with myself: Oh, she's complaining about pain again, what is it this time? I bitch at myself. Just take X drug, it's been FDA approved just for fibromyalgia! So has Y drug! The FDA is always right and knows what's best! (Sarcasm there.) Yes, and before those drugs were official, they were prescribed off-label, just like the drug I am taking now. How about that? Mm, I will stick with what my physician, neurologist, and rheumatologist prescribed. Those drugs have worked great so far (no, really, they have). Do yoga! Do this kind, that kind, this position, that position, it'll totally help! Not always. There are times when I can barely raise my arms and bend my knees simultaneously. I do yoga stretches when I am able. I take my prescriptions, I take certain supplements, I massage with certain oils.
I do my very very very best to do everything I possibly can. I have tried, I really have. And the bitch of it all is that fibromyalgia does not care. It does not care at all. It laughs at me. It moves, it migrates, it dances, it stabs, it burns, it tries to destroy. All I can do is chase it around my body and throw pain relief at it until it shuts up and fades for a while. And I hope that while is a long while, which it usually is not.
Pile that on top of cerebral palsy, epilepsy, sciatica, lordosis, migraines, asthma, Raynaud's, and sensory integration disorder, and, well.
And, well.
That is all.
I do not know what else to say.
I am very tired.
I should go to bed now. My husband will be home in a few hours. He has been in New York City since Monday, setting up computers and equipment for a job, and when I spoke to him a few minutes ago, he was waiting on a pizza so he could bring home a piece of my old home for me. That does make me feel better.
(No, it does not feel like heart pain.)
Someone suggested costochondritis. I don't want to think about cartilage inflammation. But it is a common syndrome attached to fibromyalgia; the majority of people with fibromyalgia will develop it. I don't think I have it. But I do need to see my doctor soon, so I will ask to be checked out.
http://www.geocities.com/lynndebeal/CostoPain.html <-- I love this webpage, it makes me smile.
NOTE: The following bit of venting is not aimed at any of you. It is aimed at me, myself, only.
Also, I am tired of this. I am tired of feeling as though I walk on eggshells with myself: Oh, she's complaining about pain again, what is it this time? I bitch at myself. Just take X drug, it's been FDA approved just for fibromyalgia! So has Y drug! The FDA is always right and knows what's best! (Sarcasm there.) Yes, and before those drugs were official, they were prescribed off-label, just like the drug I am taking now. How about that? Mm, I will stick with what my physician, neurologist, and rheumatologist prescribed. Those drugs have worked great so far (no, really, they have). Do yoga! Do this kind, that kind, this position, that position, it'll totally help! Not always. There are times when I can barely raise my arms and bend my knees simultaneously. I do yoga stretches when I am able. I take my prescriptions, I take certain supplements, I massage with certain oils.
I do my very very very best to do everything I possibly can. I have tried, I really have. And the bitch of it all is that fibromyalgia does not care. It does not care at all. It laughs at me. It moves, it migrates, it dances, it stabs, it burns, it tries to destroy. All I can do is chase it around my body and throw pain relief at it until it shuts up and fades for a while. And I hope that while is a long while, which it usually is not.
Pile that on top of cerebral palsy, epilepsy, sciatica, lordosis, migraines, asthma, Raynaud's, and sensory integration disorder, and, well.
And, well.
That is all.
I do not know what else to say.
I am very tired.
I should go to bed now. My husband will be home in a few hours. He has been in New York City since Monday, setting up computers and equipment for a job, and when I spoke to him a few minutes ago, he was waiting on a pizza so he could bring home a piece of my old home for me. That does make me feel better.
no subject
Date: 2009-03-12 04:16 am (UTC)no subject
Date: 2009-03-12 06:02 am (UTC)no subject
Date: 2009-03-12 03:12 pm (UTC)Your self care regimen is good... some day will be better than others, other days need more gentleness for yourself. I'm working on this, too, and empathize daily for you & the discomfort levels you deal with. big hugs....
Hope your pizza was yum!
no subject
Date: 2009-03-12 05:36 pm (UTC)One reason I am trying to be polite as frak when people say "CFIDS? Oh, try an SSRI." Um, tweaking dosage w.r.t. the one I'm on does bad enough things to my head. I'll find alternative therapies, thanks.
Your list of comorbidities makes medication of any kind a calculated risk at best, I should think. You seem to have a care team that really does know how to manage things. (Insert mild envy...) Trust 'em, lovely.
♥ you.
no subject
Date: 2009-03-12 11:55 pm (UTC)Thanks! After reading so many horror stories from patients with epilepsy, fibro, CP, diabetes, etc etc... I find myself profoundly grateful to be able to work with doctors who really care and really listen and want to understand
How do you make the heart? I want make the heart back at you.
no subject
Date: 2009-03-13 12:12 am (UTC)The heart is & hearts ; but without the spaces. Like so ♥
no subject
Date: 2009-03-13 12:26 am (UTC)Oh, like this? &hearts
no subject
Date: 2009-03-13 02:10 am (UTC)Wellbutrin actually alleviates them. :-)
no subject
Date: 2009-03-13 02:15 am (UTC)I've recommended Ashwagandha to friends who didn't want to take prescriptions to boost their libidos, and it seemed to work. One friend gave some to her dad, who was experiencing erectile dysfunction, and it actually worked for him. I was stunned.
♥
no subject
Date: 2009-03-12 05:55 pm (UTC)please take care of yourself.you'll be in my thoughts.
your husband has been in NYC.I was just writing about how I wanted to take a group trip there one day!if it ever comes true,I will send you and your husband tickets to come on an NYC adventure!
feel better,stay well and I will send you good healing energy.
no subject
Date: 2009-03-12 11:56 pm (UTC)NYC is my home, at heart. I was born in Brooklyn and raised within the city. It will never leave my soul.
no subject
Date: 2009-03-12 09:34 pm (UTC)