Fibromyalgia Support Group
You're not alone in your pain. Fibromyalgia is a condition that can be difficult to diagnose and manage. If you're trying to cope with pain throughout your body, sleep problems, general fatigue, or other common fibromyalgia symptoms, you're in the right place. The community is here for you to talk about therapies and share your challenges.
Alternating heat and ice, rest, keep up your water intake are the best you can do. If you can take Ibuprofen, it can be beneficial. Don't tolerate it myself, but I do take Tylenol ES to take the edge off the pain if it gets really bad.
Best of luck to you and know that you are not alone in this!
Voltaren is a medicinal gel, available over the counter. Generic name is: Diclofenac diethylamine gel 1.16%. Some pharmacies also have Diclofenac 10%, but that requires a prescription. Works great!
I'm amazed that there isn't a costochondritis group here on DS - we have so many people in this group who have it, and there must be many more.
Hope the pain is under control quickly.
I want to curl up in a ball when this happens. In fact, I've just spent the last two days doing just that. Trying to find a position where it doesn't hurt to breathe.
I've had lower back pain just about all of my life and I'm used to it; I can handle it. But the upper back pain is different. It just makes me feel like I'm going to cry.
I, too, do the ice/heat therapy along with Ibuprofen. The past two days that didn't even take the edge off the pain.
I'm going to explore the other remedies named in these posts, and I'm grateful there is a Costo community, even if it has to piggyback on the Fibro site.
And, yes, I am VERY surprised there is no Costochondritis group on DS. I've already put in a request for one, so here's hoping.
I was going to write about this then saw your post. Recently the Rheumatologist confirmed through blood testing that I have it. So, I was treated when it was really bad by the Cardiologist by Colcrys and Indomethacin (a strong anti-inflammatory). Did this for 30 days and wow, it knocked it out. Now, it's baaaack after 4 months and the Rheumy has put me on Sulfasalazine twice a day. I'll let you know how it goes.
Sorry, I wish I knew how to speed it up too...but I do feel for ya, literally! Hugs, JP