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Re: Update from Antoinette

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It is good to know she and her family is doing good. I do miss her

support of the STRONG SCD. I really need to know that there are

others out there that follow SCD in its completeness.

Hope she startes posting again soon.

Sandy M.

>

>

>

>

> >> Kiki is having MANY BREAK THROUGH in speech. When she gets a

word

> >> wrong she stimms a little, but you have to understand that just

a week

> >> ago she wasn't even trying to use spoken words that much. Yet

was

> >> finally wanting to learn sign language. Which in itself was a

huge one

> >> for her! WE are so THRILLED! She hasn't had a seizure since

her

> >> hospitalization end of May...we are thrilled about this too!

With just

> >> SCD she is on the right path again.

> >

> > SCD 2/06

> >

>

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Carol, I guess I am confused. I thought that this is what Antoinette

did with her family.

Are you saying that she couldn't do that anymore so she decided to not

post anymore?

Sandy M

>

> I follow the original SCD and am doing very well but not everyone is

> able to do the adult version.

>

> Carol F.

> Celiac, MCS, Latex Allergy, EMS

> SCD 6 years

>

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Carol, are you telling me that she is not posting because she felt

she was confusing people or that she is not being allowed to post?

I hate to be dence but it seems like the questions are being

skirted. Am I in danger of not being allowed to post if I tell

people that we have had good results with Tobias with SCD, a few

supp. and on enzeme?

I guess I am still pretty knew at this message board stuff and how

it works.

I saw a post by not very long ago that gave links to sites

that he had developed that went totally against what BTVC teaches.

Besides he is rude and crude. How does this all fit together.

Sorry but the more I read and write, this is really beginning to

bother me!

Sandy M.

>

> > Carol, I guess I am confused. I thought that this is what

Antoinette

> > did with her family.

>

> Sandy,

> Antoinette frequently stated that SCD with autism adjustments did

not

> work for her and she suggested people try SCD without them at

first.

> This could be misleading to newcomers who may only have been able

to do

> that as they began to heal. Some do better with supplements and

enzymes

> and are not able to manage without them. Elaine realized that a

single

> approach did not always work unilaterally and had tolerance and

> flexibility about things that would help implement the diet

optimally.

> That's why there is a Pecanbread and why Elaine participated when

it

> was " Elaine's Children. "

>

> Carol F.

> Celiac, MCS, Latex Allergy, EMS

> SCD 6 years

>

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Summer, I am sorry if I offended you. I did not see much in the

sites that posted to line up with SCD and he has very

demeaning to some of the moms at times on this board. As you know

most moms that have put the work into even starting SCD don't need

to be told that they are to lazy to read for themselves. Yes,

they/we/I am looking for a quick answer at times because they are to

exaughsted to search every detail for them selves. I guess I

thought that this was part of what pecanbread was about support and

exchange of ideas/support. Maybe I am wrong and at the wrong place.

Be blessed to all.

Sandy M.

> >

> > > Carol, I guess I am confused. I thought that this is what

> Antoinette

> > > did with her family.

> >

> > Sandy,

> > Antoinette frequently stated that SCD with autism adjustments

did

> not

> > work for her and she suggested people try SCD without them at

> first.

> > This could be misleading to newcomers who may only have been

able

> to do

> > that as they began to heal. Some do better with supplements and

> enzymes

> > and are not able to manage without them. Elaine realized that a

> single

> > approach did not always work unilaterally and had tolerance and

> > flexibility about things that would help implement the diet

> optimally.

> > That's why there is a Pecanbread and why Elaine participated

when

> it

> > was " Elaine's Children. "

> >

> > Carol F.

> > Celiac, MCS, Latex Allergy, EMS

> > SCD 6 years

> >

>

>

>

>

>

>

> Summer's Family, SCD 08/04

http://health.groups.yahoo.com/group/openblooms/

>

> ---------------------------------

> Groups are talking. We're listening. Check out the handy changes

to Yahoo! Groups.

>

>

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Hi Carol and listmates,

> This may be a part time community but it is still a community. If

> someone was excluded because he or she could not be civil and

> respectful of others than they deserved it. People here bear more

than

> a normal burden and have a lot of issues to keep straight.

>

....> Let the moderator (s) maintain decorum and let's please get

back to why

> we are all here.

> The children deserve nothing less.

>

I believe Carol said it quite well, so for the sake of the children

and adults regaining their health, please keep the name calling

offlist. If a person has issue with something that another posts

please address the issue without insulting the person or contact me

or one of the other moderators offlist.

The purpose of this list is to help guide and *support* those

implementing the SCD.

Sheila, SCD 2/01, UC 22yrs

mom of and

Pecanbread moderator

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