Trigger point injections ( Chinese medicine )
Cold pack near the feet when I go to bed
The on line support groups and my husband have been my lifeline.
Walk as little as i can. Allways put my feet up in the air, as often as i can.
9 X 20 inch gel ice pack to put around my feet and legs
Taking ALA (Alpha Lipoic Acid)
Meeting others like me we all can empathise as we are all linked with raynauds em scleroderma etc
Being believed
Lying still in bed
elevating affecting limbs
Less stress seems to improve my over all flares.
Portable climatisation
family support
BupropionXL300mg
Keeping my house and myself cool
Exercise - walking at a slow pace daily
venlafexine has also been helpful
Taking Cymbalta.
Magic bags from the freezer
Cold Towels , air conditioning and fans which keep the air moving around me
cool water soaks
Also lots of love from my friends and family is what gets me through the day.
Acceptance and a fantastic husband .
Stay off of feet
THC/CBD
Open shoes
Salsalate
Climate controlled the house with a reverse cycle air conditioner/heater - big power bills worth it
Ice packs used for autonomic dysnomia to cool core body temp down
When It is cooler....like now
Meditation
Soaking in cold water when flaring
Lanacaine spray when I can't stand it anymore
Maintaining as cool and humidity free environment as posible
Finding support online with other sufferers
Ice
My very patient and loving hubby
Exercise. I walk of a night time when it is cooler.
Water in a bucket
Reading on line that Lidocaine patches can help with the pain
Eating healthy
taking Xanax to get good sleep
Avoiding certain foods and drink
giving up work
My kids inspire me to keep going
Peppermint lotion on flaring areas provides cooling without the damage of ice
Ice packs