I have Myofascial Pain Syndrome. Recently diagnosed, and trying to figure the rest out. Anyone else out there? Tips? Advice? My primary couldn't care less unless someone else is there to call her out. I'm sick and tired of not being able to do a lot of things that I used to do. I can barely get dressed most days. I'm sorry for the rant.
Sweetheart, a lot of us feel like you are now. It's all about adjusting to finding the same you in a different way. Pain. Dr's don't care about your pain. They say it won't kill a person but lots of people commit suicide who have constant pain. I say it kills. I personally am lucky it's taken me a lifetime to be disabled from fibromyalgia and it keeps getting worse but I found a red African tea called kratom. I buy it in bulk capsule form because I can't take the taste of the traditional manner of ingestion. Read on it and other natural stuff that actually helps instead of being dependent on opioids and worse. My point is find what works for you and simply keep trying to live your life in whatever form that you can. We just keep moving I think. Trying to be positive. I hope you do well.
Excellent advice and props to you for finding natural pain relief and what works for you @Tiny! @Nonbinary...try not to lose hope or get too frustrated. There is something out there to help you! ♥️
Have you tried myofascial release yet? It’s helped me greatly in getting the pain down to a tolerable level. I’m so sorry you’re in awful pain. I’m joining you—- from my couch to yours, on a perfectly lovely Friday night 🤣
☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.
Share
Copy Link
Copied
Join the Alike community
Discover your Alikeness™ with people who are on the same journey, gain wisdom and get emotional relief in a secure & anonymous space.
NonbinarySlytherin
488d
I have Myofascial Pain Syndrome. Recently diagnosed, and trying to figure the rest out. Anyone else out there? Tips? Advice? My primary couldn't care less unless someone else is there to call her out. I'm sick and tired of not being able to do a lot of things that I used to do. I can barely get dressed most days. I'm sorry for the rant.
1
5
Share
Abdominal Distention
Fibromyalgia (FM)
Generalized pain
Tiny
488d
0
Tiny
488d
0
Jess1980
488d
0
Fiesty
485d
0
Jawbreaker
340d
0
☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision