MCAS: Mast Cell Activation Syndrome (or Disorder)

Thread Tools

Display Modes

02-06-2016, 02:27 PM

#11

SylvieM

Member

Join Date: Nov 2015

Posts: 129

SylvieM

Member

Join Date: Nov 2015

Posts: 129

Quote:

Originally Posted by stillHoping

Hi Sylvie,
There is an exercise training program by Dr Leviene from Dallas that might be helpful for POTS.
http://www.sciencedirect.com/science...66070214002021
You can read about it in this blog -
http://potsgrrl.blogspot.co.il/2011/...-protocol.html
There is a lot of information about tests and treatments for POTS in that blog.

According to what you wrote here and on previous posts, if your blood pressure is falling when standing, I am not sure the diagnosis is POTS, as far as I know it seems NMH/OH.

I have both....as noted by En Boc, they are interrelated. I've heard about the Leviene protocol, but have not read anything except patient experiences....thank you for these references!

Reply With Quote

Tags

allergies, dysautonomia, mcad, mcas, sfn

« Previous Thread | Next Thread »

Posting Rules
You may not post new threads You may not post replies You may not post attachments You may not edit your posts BB code is On Smilies are On [IMG] code is On HTML code is Off Forum Rules

Similar Threads
Thread	Thread Starter	Forum	Replies	Last Post
palmitoylethanolamide : a mast cell stabilizer	boytos	Peripheral Neuropathy	6	02-23-2011 01:22 PM

All times are GMT -5. The time now is 01:58 PM.

NeuroTalk Forums

Helping support those with neurological and related conditions.

All posts copyright their original authors.

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.

Always consult your doctor before trying anything you read here.

Site Navigation

NeuroTalk Online Support Groups

MCAS: Mast Cell Activation Syndrome (or Disorder)

NeuroTalk Forums