structured routine
Strict graded exercise regime with an exercise physiologist to improve physical tolerance
I was eventually diagnosed by a neurologist in 2010
Be patient. Your body needs time to recover
My son giving me purpose to wake up every day
Resting and don't overdo it
Learn the love languages of those closest to me so I can use my limited energy in the best ways possible to nurture my primary relationships
My family are quite supportive
Saying no
I work to educate the public about ME/CFS.
Colchicine; Kenalog injections
My significant other
Diet
better sleep
Family support
I use inner ear plus from CVS for ringing in my ears and for the stuffy feeling in my head
Being in support groups
Take out food
Not feeling guilty
Having a support group helps. Looking for local people with CFS.
Pedialyte (non flavored)
Eat as natural as possible. The less processed, the less digestive issues.
Careful management of PEM
Pacing or regulating my activity, still a work in progress. Seek to work when I can not when I have too.
Massage therapy (Frequent)
My family's, and especially my mum's constant support and help
For some reason I always feel better after drinking aloe vera drinks
Epsom salt baths with lots of Epsom salts
My little dog that keeps me company
Avoid sugar, alcohol, take away foods,
Co-morbid POTS diagnosis and treatment with beta blocker and electrolytes.
Cousins became involved to coordinate/educate new doctors
Cutting drama out of my life as much as possible
Some of my family & my friends
chiropractor
Music and movies
Hydration
Accepting i cant do much anymore
Family support/support groups online
Regular deep tissue massage
Understanding
Perrin technique & Acupuncture
Rely on care from my husband
Drinking alkaline ph balanced water
To be able to eat properly
valtrex
Dietary changes
Meal Prepping on good days made eating healthier easier on bad days