Re: Mercola protocol and scleroderma

[Guest guest]

Dear Schulz,

1. As far as doctors tell me I do not have Scleroderma, I am however

interested to learn more on effective treatments for autoimmune

diseases (as apparently they share a common thread ... ?!), I went

to http://www.mercola.com , IS IT THIS WHAT YOU ARE REFFERING TO?

Can you send link on where he refers to Scleroderma precisely? I

want to share such info with someone I know.

Do you plan to go to the Clinic in person? Where would be the brick

and mortar address, again IS IT RELATED TO the above site?

The person I know and has Scleroderma tells me is trying diets. I

posted my (limited) understanding about this subject and diet at

http://www.philfrisk.net/~adrian/topic_ap_amd_mp_for_Scleroderma.htm

From what my friend does (as she is a doctor herself) you may be

correct thinking of diets – what Dr Mercola seems to be about. I AM

STILL WAITING TO FIND OUT WHAT this friend of mine thinks of Dr

Brown and Dr Marshall Protocol, etc .

Regards,

> My question is:' Did anybody with systemic scleroderma went yo the

Mercola clinic and got help? Thank you very much.

>

>

[Guest guest]

I found a good intro of Dr Mercola at

http://www.mercola.com/forms/nptour/

I found the brick and mortar info address at

http://www.mercola.com/forms/nptour/#locdir

In practical terms I really try to (and often succeed – to get

better and better on this …) eat at lest some green with each meal,

and posted few personal thoughts about Normal, Vegetarian and

Naturist foods at

http://www.philfrisk.net/~adrian/topic_ap_amd_mp_for_Scleroderma.htm

Regards,

> My question is:' Did anybody with systemic scleroderma went yo the

Mercola clinic and got help? Thank you very much.

>

>