One day at a time.
Still going strong.
Still going strong.
looking forward to anniversary.
I'm not sure why, but despite all the unrest in the world, and despite my physical challenges, I feel more hopeful than I have in a very, very …
forgot to mention I am also a member of the AlAnon One Day At A time group! LOL
Big hugs.
hey sweetie...I got rhuematic fever when I was 7 years old...my sister said one day I got on the couch and couldnt get off...my joints swelled so bad I couldnt move from neck down...I spent 3 months in the hospital...I remember getting 13 shots a day and penicillin...penicillin penicillin...I have low immunity today...I had problems with my heart like attacks twice a year til I was about 12...I was diagnosed with fibromyalgia in I think 2004...of course I had it before hand it kept getting worse and my pain management dr diagnosed it and put me on nortripyline and then they closed the clinic and I lost my dr...not too many drs here that acknowledge it exist...in the northeast corner of CT...
hi Daisy Mae...would like to connect..we have alot in common...age..we have been on ds about the same time...the rhuematic fever as a child, the fibromyalgia and so on...would like to connect and add you to my friends list if that is ok...hugs and let me know...Debbie
Hi Daisy, I am so sorry your husband does not understand us. I have had FM for over 20 years and my husband is just now understanding my limitations. We had many years that I just acted like I was ok until I crashed. Just remember you have to take care of your self and stress will and does make your FM much worse. Take Care!
My family of original struggles with alcohol. They know me as the one with the problem. I have gone two years without drinking, and loved it. Thought it would help the pain of fibro go away, but only creates bigger problem...gotta quit for good!
In 1991 I started developing symptoms (after head on collision with truck). Over the years, the nature of the pain keeps changing, worsening, I want to know how to mediate the pain. And how should I plan for the future...
I have undiagnosed pain. Five years ago I had major relapse, and all they did was give me morphin for pain, and physio to get me back to work. I was not satisfied then, nor am I now, as I have different pain now that radiates down backs of all four limbs, debilitating pain. Why can't they test me for MS just in case they can do something to help, rather than just let me keep suffering. I'm not sure what the first steps are.
Today my doctor said that her "best guess" is that I have "chronic pain syndrome". I have been seeing her regarding pain for at least ten years, and I want a diagnosis so that I can plan my life. The pain keeps changing, and is just getting worse. It is my biggest secret in my life and I need to be able to call it something so that people around me understand.
My husband has sleep apnia, and is doing nothing about it. I am joining this group in hopes to find solutions.