Ever heard of LDn improving OI/POTS for ME/CFS?

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Howdy folks,

I tired the ldntrust.org forum but haven't seen much action there

but I DO like their videos..

Anyway, I like the amount off activity I see here

I'm at the end of my 2nd week at the 1/2 tab=1.5mg per night dosage,

my 1st lowest level (eventually maybe 3mg, then 4.5mg)

Anyway, for the last 2 days I am suddenly after 3 years NOT expierencing

my " usual " OI/POTS symptoms when Vertical, but am having some

rapid heart beat, cold/hot flashes, and nerve tinglings (all I can live with)

BUT, what I AM wondering is...

Has anyone heard of OI/POTS symptoms in ME/CFS patients

suddenly abating? cuz this would be a HUGE Miracle

and a Real Life-Changer... if this has happened before....???

Would REALLY Appreciate any input.. Thx muchly..

Almost getting EXCITED, but not wanting to quite YET..ya know?

Thanks for any replies