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I told myself this year I am to take better care of myself!!! So far I've been very slow at it ( for obvious reasons) NO more excuses; I am my top priority!
So please tell me what it is that helps you feel better and relaxed or pampered??! Do you use expensive/quality shampoo conditioner??? Get you nails done??
Button line what's your "GO-To" for self care???? Beyond medication.
@A MyFibroTeam Member Have thought of you sweetheart
You are a true warrior honey and overcoming so very much. Self care is so good for you
Good to see you around once more. Take care my dear… read more
Itchy sores on scalp. Took a round of antibiotics. Back
It is much worse for the person experiencing it
Just working with wounds really made me more conscious
It's crazy what a little cut can turn into. Now, I always clean stuff like that right away and… read more
Help needed.
Hi Liz. I so do understand you. I too am alone with no family or friends and Fibro so bad I can barely walk. I have no answers. I am extremely depressed and wish I could find a way out of all… read more
On as we all know one symptom of fibromyalgia is dry skin
Well mine is beyond dry and gets to the point of cracking and bleeding and nothing I use seems to work
What sis the best moisturiser to use for extremely dry skin
I’ve tried Vaseline intensive care and now using Nivea but to no avail
@A MyFibroTeam Member @A MyFibroTeam Member
I tried the conditioner all over my body and I have to say that really does help. Thanks for that tip.
Hope you're having a good day.
Hugs ❣️
Sandy
Hi all, I am newly diagnosed. I seek Naturopathic care for most everything. My PM&R Doctor wants to put me on Lyrica. Who has tried it and which of the three do you take now? Thanks!
Lyrica made me a zombie, made me more depressed. Please look for different option. Really, not kidding. (((hugs)))
I’m just curious if anyone can share they have knowledge or experienced any of the results from a CPAP, which mine came back pretty severe.. then I had an oxygen test done and it’s coming back that I need home oxygen care just curious what your experiences strength and a little bit of hope we all need
Thank you so much I appreciate it
Right now I live with my mom and her boyfriend, my mom is essentially an unpaid caregiver for me. I'm hoping to move out but I don't think I could be completely independent on my own. I've been looking into the process of getting a caregiver, and I'm planning on my mom sticking with being my caregiver, just getting paid for it finally. Does anyone else here have a caregiver, officially or unofficially? What are your experiences like?
Where are people with fibro doing since this happened?
Yes. Musculoskeletal neurologist is who I see. He is great and knowledgeable.
Hi everybody I just want to ask as anybody been dynnosed by a consultant for there condition.
Then refer back to your local Doctor to manage your pain?
If so have you been question by ESA medical assessment if you are still under care from consultants.
And if not why and GP does not count managing your care?
ask the doctor to refer you to pain clinic
e.s.a assessment give them the consultants name and they will deal with it x
The fibro pain is overlayed with this sensation. I went to dr, and blood pressure is high. 140/90. I’m always in the 120’s 70’s. Is this high blood pressure sensation? I have NO insurance, and now my primary care dr is sending me to a neurologist. I can’t afford wild goose chases, any thoughts anyone. Thank you for any answers.
Sometimes jerks wake me up at night.
