Quick Links
About MySpondylitisTeam
Powered By
Hi, I've a low red blood cell count, which I realise can be linked to chronic inflammation and AS, and I suspect could be significantly influencing my fatigue & brain fog. I'm not wanting to go on medication, but does anyone have any advice or experience of similar and how they resolved?
Thanks both, much appreciated
Yes, it took me 6 months or more of physio before full relief. I keep doing at home every day what I learned and it has not returned. That was about 6 or 7 years ago.
Polymyalgia
Thank you.
@A MySpondylitisTeam Member. What kind of problems?
I don't think so. Diminish inflammation. Biologic is suppose to slow down the progression.
Thanks for the advice!!!
I've been sleeping and have a spasm in my face, (it's not new) and I realized I'm biting down on the back of my tongue. When I first noticed it, it was on one side. Now it's both sides. It wakes me up. Does anyone else experience this?
I have had this happen. The first few times it woke me and I was afraid to go back to sleep. Does it feel like you jaw snap shut very suddenly? That is how it happens with me. Iβll be asleep and itβsβ¦ read more
Nature's Bounty
I have no problem taking meds that help me but the prices are ridiculously expensive like 3,000 a month so I said no, cannot afford and even though the meds do help with slowing down the progressing I have to say no. Does anyone taking these meds.
In canada cosentyx have a program for helping with the expense. They send me 3 seringue for christmas. And it change my life. Not perfect yet but cannot live without it.
Continue with Facebook
Sign up with your email
Your privacy is our priority. By continuing, you accept our
Terms of use, and our
Health Data and
Privacy policies.
