Mast Cell connection to POTS, EDS, Chiari, possibly MS and others

[Guest guest]

Dear All,

First of all, thank you for introducing the group today,

to the possibility of Mast Cell involvement in our problems,

how right I think you are!! It's a topic I've been SOOooo busy

investigating myself. Having spent the last 2 weeks trying to

get my head around it, I feel very encouraged (and excited) by

what I've learnt.

The latest research I think, will connect many, if not all of

our symptoms to a set of unfortunate bodily circumstances,

previously undiscovered (that we are probably all suffering

from, to one degree or another). It's not 'just' Mast Cell

Activation problems - that's only part of the picture.

This is GREAT NEWS, as it gives us hope for the future

(particularly to those of us that can't get surgery).

The new treatment protocol that's being developed, will

hopefully lead to much better management of our symptoms,

so that we can gain control of our bodies once again.

The best information I have found on this subject, is

included in an extensive study carried out by a member of

the medical profession, a Dr Driscoll, who suffers

from the condition herself (and her children) - what better motivation can you

have, to find the answers!!!

It's called The Driscoll Theory, take a look at her web-site

www.prettyill.com. You can download a copy of part 1 for free

from this site. If you want the more detailed version, part 2,

you'll have to download it via Amazon - but it's a very low

price, so don't worry - and worth every penny. There are lots

of informative videos on Dr 's web-site. I'm sure you'll

find some answers there.

Regards

Barbara

(UK)