Mere, sorry you are feeling funky.....such is life with dysautonomia....I have developed SVT and they have me on a small beta blocker dose, which in my opinion is not helping matters....I can still feel the rapid take offs, which they say are up to 250-300bpm (but not sustaining). I have accepted the fact, that I am going to take a digger one of these times I get a gray out.

Foo is all I can say. I will say a foo for you too....that would be foo, foo. (Sounds like a French poodle name.)

Hang in there. This crud comes in waves. I agree with MRSD.....check the meds.

I went shopping today, with my friend of 25 years, who has sarcoidosis....I say the only thing worse than being me, is being her.....she says, it is worse to be me. I dunno.

She got breathless trying on dresses (mother of the groom) and I couldn't help with the zippers....could not see, and could not grasp the zippers and clasps. I laughed and reminded her we used to bike 30 miles at a pop years ago, and now, we are exhuasted trying on gowns! Foo, foo....and one more foo for her too!

I wonder why so many of us are sick??? (With roughly the same crud.)