Guest guest Posted July 18, 2006 Report Share Posted July 18, 2006 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 > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2006 Report Share Posted July 19, 2006 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 > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2006 Report Share Posted July 19, 2006 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 > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2006 Report Share Posted July 19, 2006 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. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 20, 2006 Report Share Posted July 20, 2006 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 Quote Link to comment Share on other sites More sharing options...
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