Need to talk to someone suffering from summertime dysautonomia
with Lyme disease.
ER's don't understand a thing
and sometimes my nebulizer doesn't help at all
and get short of breath after urination...
get bp all over the place...
can't breathe outside in heat at all
and start shaking like crazy in heat and want to faint
even if not dehydrated...
praying to be able to make it to my LLMD
any coping ideas/strategies in the meantime???
thanksso much in advance