"Thank you all... My Mom was double jointed maybe that's where it came from. I don't think it's EDS but will try to remember to ask my rheumatologist about it. It's just frustrating not knowing which symptom goes with which disease. :)..."
fortywhat2's Profile
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About Me: Female, 66, E Wareham, MA, member since Jan 2009
I was diagnosed with PPMS (primary progressive multiple sclerosis) 8/08, they said I have probably had it for 10 - 20 years. I was diagnosed with fibromyalgia a few years earlier, Hashimoto's Disease a few years prior to that, and Osteoarthritis many years prior to all
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of them. There are many autoimmune diseases in the family but no m.s. that we are aware of.
I had to leave my job of 13+ years as a medical office manager due to cognitive deficits and reduced processing speed.
My motto...
~live as if all your dreams came true~ [Less]
I had to leave my job of 13+ years as a medical office manager due to cognitive deficits and reduced processing speed.
My motto...
~live as if all your dreams came true~ [Less]
Interests:
progressive, cognitive, deficit, autoimmune disease, Arthritis, Migraines, Nutrition, Pain, Chronic Pain, Thyroid Disorders, Weight Management, Diet and Nutrition
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, Exercise and Fitness, Multiple Sclerosis, Fibromyalgia, Osteoarthritis, Back pain, weight loss surgery, Vitamins & Supplements
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Best Answers: 2Top Answerer:
Neurology
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Apr 28, 2014
"Good Morning All...
My Rheumatologist that I see for my fibromyalgia told me that all my joints are hyper extended... I wonder if anyone has that same problem. I'm wondering if this is possibly MS related and not fibro at all. Oh yeah..."
Hello all...
I'm doing my annual spring- time bounce in. :). I hope everyone is well, or as well as expected! I am in FL visiting my Dad... We had our first annivers...
Hi everyone,
This must be my springtime bounce in :) I hope everone is doing well! Quix, I am sorry for your loss (I just saw a post) I hope you find comfort in your ...
Hello everyone,
It's been a long time... long enough so I'm very confused with the new format. Let me update my life... I had gastric bypass surgery in December....
Mood Tracker Stats
03/13
Be sure to see my followup on the NBA.tattoo comment. No malice was intended on my part - in fact my daughter has about a dozen tatts now, each a piece of wearable art.
10/11
Thanks for sharing. I think I probably need a new neuro, too. We have hardly any here in Colo Sprgs. The other big one here in town takes 7 mos. to get in to see him. He was the 1st one I saw, & he never even moved me over to MS from transverse myelitis, even though I also have brain lesions. Then I was seeing a neuro in Denver at the Rocky Mtn MS Ctr & he gave me the MS Dx, but he's an @$$....
10/11
Hi Debbie, my neuro says that since I can still walk after 2 yrs of symptoms, then I don't have PPMS. According to her, if you have PPMS, you won't be able to walk after 2 yrs (even though I've never had a flare - just a slow decline). I think she's flat out wrong. I have problems walking up hills & stairs and walking too long. Are you still able to walk?
09/11
Just a quick note to say hi Thanks for checking in - I hope you have found a way to live with this craziness. hugs, L
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