Fw: [mb12valtrex] Topics for the mb12valtrex list

[Guest guest]

Marcia is stirring up a DAN list!

----- Forwarded Message ----

From: and Marcia Hinds <hindssite@...>

mb12 valtrex

Sent: Wed, August 25, 2010 9:18:30 AM

Subject: [mb12 valtrex] Topics for the mb12 valtrex list

Cheryl,

Your post concerns me. Aren’t we all here for the same thing? To find

answers

for kids with Autism. Bill is simply stating research and what worked for his

kid and has no financial incentive for doing so. I can’t say the same for

Stan

Kurtz (who also was a patient of Goldberg). He is making a living off his

kid’s

autism. It infuriates me that he is not a medical doctor and yet I’m told

charges $200/hour for a consult with parents. What is wrong with this picture?

Those of us following the protocol have nothing to gain by posting here.

We just want to help kids. I once made a promise to God. You make mine better

and I will work to make them all better. So I have to live up to my end of the

bargain. McCarthy in her own book admitted that her son was not doing

well but she was going on TV promoting her parenting book to bring in the bacon.

You openly admit that Dr. G helped your kid. I understand why you left. Dr. G

can be difficult to work with. I left myself for several years after getting

tired of arguing with Dr.G. But the reality is, he is right in his medical

protocol and the best at the medical issues. I still don’t agree with him

behaviorally or educationally. But if even one kid benefits from what Bill said

it should be posted. Open discussion and dialogue and difference of opinion is

the how things should work on any list.

Marcia Hinds

I'm going to have to say that I'm going to have to defer to the title of the

list here. Everyone that joins this list has an opportunity to read the home

page description. This list is to discuss biomedical treatment options and is

for those looking at MB12, HBOT, Chelation, etc. Sooo, my point here is that

this is not the place for this discussion. Please take it to the list or

offlist.

Just in case anyone has forgotten, here is an excerpt from the message on the

Home Page:

This private research group, started by Stan Kurtz, a parent of a recovered

child, offers parent support for people who are interested in the new Revitapop

Methylcobalamin (MB12) Lollipop, nasal spray MB12, Valtrex, natural antivirals,

virastop, Olive Leaf Extract (OLE), LDM100, antifungal therapy, bacterial

therapy, Hyperbaric Oxygen Therapy (HBOT), and diet for anti-infectious therapy

and chronic illness including autism, ADHD, fibromyalgia, asthma, eczema,

chronic fatigue, hypotonia, mitochondrial dysfunction or disorder, sensory

integration dysfunction, dyslexia and other chronic illness.

If these things do not apply to you, I'm not sure what made you join the list.

I don't want to hear any more about how supps are bad, b12 is bad, chelation is

bad, etc. If there's something constructive to say regarding any of these

things, feel free to do so, if you have experience with these things, feel free

to say it. But no more discussion of how everything is wrong but . I'm done

moderating it, I'm done getting the complaints. This list is for those that are

actually doing those things and I'm not going to continue reminding people of

that. If you are looking to discuss , there's a list for that and they

are very supportive and willing to help and answer questions. I know because I

used to be on it.

There was nothing particularly wrong with Bill's post. I'm not mad, I'm just

tired of dealing with this. I'm tired of having to remind people that while

may not like these things, this is not a list and I would appreciate it if

the attempt to turn it into one would end. I'm not killing my son by giving him

Vitamin C, thankyouverymuch.

It's over. No mas. Anyone interested can join the list, there's no law that

says people can't join multiple lists (I myself belong to about 20). But take

the discussion there or offlist.

I will start moderating people and deleting posts. If I have to delete too many

posts, I will start removing members. I repeat, this is *not* a list. Take

it there, please.

But I did appreciate Dr. Klimas's explanation, very informative. I wish it had

been left at that and this e-mail didn't have to be written.

Cheryl

~http://www.gryffins-tail.blogspot.com <http://www.gryffins-tail.blogspot.com>