B12 injections 1 / month
Listening to music
Several yrs on SSRIs
Resting in between activities
Massage Therapy
Valcyte allowed me to go back to work 30 hours a week after being disabled for 10 years but when I stopped due to liver issues, I went back down hill.
Being given a sleeping aid to be able to rest at night
Retiring from a physically demanding job.
Positive attitude/being grateful for what I do have.
Limiting what I do. Not filling up a weekend with things that will exhaust me on Monday. Learn to say no. Pick your windows.
Probiotic
Diet: Low inflammatory Diet, Probiotics, Salt, Caffeine (Coffee/Tea)
Magnesium/taurine injections
Warm water therapy in heated salt water pool with no chlorine, daily
Tramadol
I have a gp/family doctor who believes in the reality of M.E.
NT Factor supplement
Exercise
using pain meds
Hepapressin, B12, Glutathione, Injections
Acceptance
Xyrem changed my life for 10 years, made me have almost no pain, didn't feel like a train had run over me every morning, but now, due to FDA, doc refuses to prescribe it!
Life style change - being really careful not to do so much.
Acceptance. Not pushing through.
Amitriptyline for sleep
Just keep trying
8 years to get a diagnosis
Knowing what I can control and letting go of everything else.
ME/CFS: Dr. Chia in Torrance, CA, USA and his treatment of Equilibrant, Antivirals, and Methodone
Sugerfree, glutenfree, milkfree diet
Ketogenic diet
Pacing my activities
After years of struggling, got Disability Living Allowance which enabled me to pay for house cleaning & meals
Support and understanding from family and friends.
Daily meditation practice for 24 years., since I got sick. Meditation allows me to change my physiology through the relaxation response. It helps balance mood, pain. And, it gives me a clear space to just be- and this gives me hope to keep going another
Pacing, never doing more than I can. short walks on days I can. (very short)
Not having to work
Stretching exercises, ideally every day; long walks when possible; swimming in the Y lap-pool (cool temp really helps pain!), general exercise when I can tolerate it, the spa and steam room; when I can afford it a massage.
Getting back to woodworking.
Floor based, eyes closed yoga
Immunoglobulin Therapy.
Learning to pace as best as I can!
Massages. Has to be at least twice a week, because it's expensive I can't maintain it.
My service dog(s). Without them I would be house-bound.
Acceptance. Accepting my disability and how it will affect my life has really helped. This isn't a cold or flu that I can get over, this is my life forever.
Nothing has helped. Chronic, progressive course. Mild 4 years, moderate 4 years, now bed bound 4 years and worsening.
A very soft toothbrush, warming it with hot water to soften bristles and using Himalayan toothpaste with Neem