So as you all know my hearing before the judge is this Thursday and I am getting really nervous. He will be looking for any little thing he can find to deny me benefits and I am afraid I am going to say or do something that will be the one little thing he is looking for and he will deny my...
Hi all. Hope all that read this are at the very least having a day they can handle. I was diagnosed a couple of years ago and i wasn't exactly in the believers camp, I have since joined said camp now. I not only have fibro I also have an undifferentiated inflammatory poly arthritis and...
I am a newbie, and I have never been so frustrated in all of my 50 years of life. In 2014 I was rear ended by a company truck, at that time I started with neck pain and headaches. I dealt with the pain was x rayed, had MRI's no problems, soon after the burning started in my shoulders, the neck...
I have at least three friends with fibro and although I have lived in constant fatigue and fog for at least 10 years do not believe I have either CFS or fibro. I think I'm an EDSer but have been sent for diagnosis to a rheumatologist in Port Macquarie. My appointment isn't until April next...
Hello all. I am a 35 y/o male that has been struggling to find a diagnosis or treatment plan for what I believe to be myofacscial pain syndrome. It started 4 years ago with a dull ache in the back of my neck and a tight band around my head. This made me start to feel dizzy a lot and came with...
Again, I know this isn't the forum for this type of thing but I need to vent and it does play into my health problems. I won't go into all the details because I would have to write a novel. The gist of it is this. Several years ago my brother in law (my husbands brother) got into a fight with...
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Hi, name is Sam, my wife Lore (Lori with an E)has had fibro since the mid 1990's. It has kind of been in remission so to speak for the past 12 yrs or so. Occasional flareups but manageable.
Lore and I have been together for 9 yrs.
In May she had gall bladder surgery that had...
I have been doing a lot of reading about new breakthroughs in fibro treatment. Some of them include using a medication that is for alcoholics and opiate users to help block the effects of the drug in their brain so they can stop using them. It's called LDN or naltrexone. People have had great...
Hey guys I'm Sophie, 24, I've had fibro for 2 years, only been diagnosed for about a month. What this means is that I've had a LOT of pain and almost no treatments because no one knew what was wrong with me. My pain seems to cling to one or two areas of the body, so I would get diagnosed with...
I was diagnosed with FM yesterday by a rheumatologist. This was after months of testing by my GP for the extreme fatigue and brain fog. I chalked the pain up to 'overdoing it' because everything started in April, when I began doing more outside yard work. A friend asked if I had considered the...
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