Sorry Bubbles I feel bad that so many people have to travel far to get the care they need.
January, my insurance company first denied me the pain patches and my rhemy had to put in a special request for them. With the special request they finely approved them. I do not use them everyday just when I can't stand the pain anymore and the pain meds and muscle relaxers are not working.
I am going to try the bio freeze. I use heating pads, hot rice packs or a relief wrap which can be heated or you can put in the freezer.
I take so many meds for the lupus that when I can try something other then that it's good.
Take care everyone
Sending healing vibes to everyone.
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