It looks like itβs still in the trial stages but sounds promising.
My wife is on it for rheumatoid arthritis, she has it bad but the trexone helps.
Just curious to what my fellow ASβers do for pain control.
How many of you use marijuana and does it help you? Or pain patches, opioids or anything else.
Thanks-π
What a great pic!
Good morning @A MySpondylitisTeam Member
I hope the day is kind to you..,
βΊοΈπ»π―οΈ
I'm taking low dose Naltrexone and all my brain fog has gone x
Has anyone tried LDN for inflammation and pain?
Yes I have tried it and I developed some bad side effects and the weight gain was quick I stopped taking it.
4 lonnnnnnnng years.π¬
I am on my second biologic. I have tried Humira and 6 most later my body attacked the meds. I am now on Cosetyx. It's been about 8 weeks and I still feel so fatigued. I was thinking depression and is it still this disease?
Stay strong warrior πͺ π β€οΈ
I take gabapentin 800 mg 3xβs daily and I know it definitely helps
I often see that people take these meds but don't know what the names of them are so I can ask the doctors if they would help me sleep without so much pain. If you take them please can you give me the name of the medication you take and if it helps. Thank you. X
Tizanadine.
I am a newly diagnosed patient with Spondylosis. My condition is very advanced, considering I'm just 33 years old. I have a plethora of non pain related symptoms all day everyday in Conjunction with my pain and limited mobility. Is this considered an autoimmune disease too?
I know AS is auto-immune as i have had it since I was 20. Spondylosis is not auto-immune.