POTS

wellbeautifulspirit

Veteran Member

Joined : Sep 2012

Posts : 671

Posted 7/12/2014 7:05 PM (GMT 0)

having a lot issues that seem like POTS as well

have to find a dr that will help...

uphill battle...

i have been getting sicker....

Binduspire

Regular Member

Joined : Jul 2013

Posts : 335

Posted 7/17/2014 2:09 AM (GMT 0)

I'm sorry you are struggling. I'm sending a hug :)

Maine76

Veteran Member

Joined : Jan 2014

Posts : 993

Posted 7/17/2014 3:09 PM (GMT 0)

Where do you live?

Janasleton

New Member

Joined : Aug 2014

Posts : 12

Posted 7/13/2015 12:35 PM (GMT 0)

wellbeautifulspirit,

POTS is the worst. I wish someone had told me this sooner, but when you find a dr that will help you, you should ask about Midodrine. It's a medication my LLMD prescribed to help with my POTS.

It's definitely not for everyone. My symptoms were rather severe. Midodrine ups your blood pressure - the first time I took it my scalp started to tingle and it felt as though I was get blood to my brain for the first time in two years. It was awesome.

Something to consider :)

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