I read on our local CFS society website that some people use Saline drips when the weather is hot to help rehydrate them. The comments I read were that people with CF dehydrate quicker than non sufferers and that we don't process salt well either. Has anyone heard of this and/or has anyone used the process of a saline drip during the hot weather? I would love to hear your thoughts.
Dx Fibromyalgia, CF, Severe TMJ, Oste
openia of lower spine, arthritis of L hip, bursitis of L shoulder and hip, GERD, Perimenopause and query RA. Deleting Dairy and sugar out of my diet was what set me on the road to recovery.
"Behold the turtle who never makes progress unless he sticks his neck out" Unknown