Guest guest Posted July 24, 2000 Report Share Posted July 24, 2000 Hi all, If we decide to slip " CFIDS/ME: The Real Story " in through the huge door with a big sign saying " Children and Family, " here are a few brief ideas on contacts and lines of inquiry/resources. Hey, if kids get CFIDS too, maybe all those complaining adult PWCs REALLY are physically sick. School: Perhaps some of our associations would support a Children and Families media strategy. The CFIDS Association of America wrote a " Guideline for Schools " regarding treatment of students with CFIDS which could be useful for administrators, teachers, school nurses and government agencies. But a guideline's premise must be believed before it is heeded. Ongoing Teacher Education should NOW be offering workshops and inservices on the special needs of these kids. They are disabled. Parents are in court fighting for their sick children. Not to be forced to return to school too soon. Not to have mandatory vaccinations. To have their children's meds dispensed during school hours. To get home schooling for their children. ETC. Few school administrators show any regard for these special needs. Few nurses have a clue how to help these kids. Medical: Dr. Lapp, Dr. Bell, Dr. Campion and Dr. Poesnecker were quoted in an article written by Patti Schmidt in the CFIDS Chronicle about children and adolescents with CFIDS. Perhaps she would help, or one of the docs would be willing to do a television program on pediatric issues. The National Vaccine Information Center has been working with parents groups opposed to mandatory vaccinations for at risk children. You can visit the National Vaccine Info. Center at: http://www.909shot.com/ If you go there, send them an e-mail asking that CFIDS/ME be listed as one of the medical conditions harmed by vaccination. Now children with CFIDS are listed under chronic illnesses (like diabetes). We're for real, World. Best thoughts, Uma Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 25, 2000 Report Share Posted July 25, 2000 hi uma! we love cats too :-) just wanted to make a little corrections here - the Guidelines For Schools was put out by the Nat'l CFIDS Foundation (NCF), http://www.ncf-net.org, not the CAA. i have about 20 of them right now. i ordered one for every school nurse in the district. i was told just one in the district office was all they needed. i still plan to distribute them in all the schools . . . in a couple states, i know that activists have been able to get grants and have these sent to every school in the district. for those of you interested, there are several lists for activism out there - CFIDS-L, me-activism@egroups, resact@egroups, there's more - i'll dig them all up if somebody wants!!! <<< The CFIDS Association of America wrote a " Guideline for Schools " regarding treatment of students with CFIDS which could be useful for administrators, >>> ~~~~~~~~~~~~~~~~~~~~~~~~~ " Would they have found nothing, unless nothing was what they wanted to find? " - Agent Dales, X-Files @}{~{<<~~~~~~~~~~~~~~~~~~~~ @}{~{<<~~~~~~~~~~~~~~~~~~~~ debbie s. - dlsherman@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 25, 2000 Report Share Posted July 25, 2000 Debbie, What you are doing is fantastic! Thank you so much for the correction and further information. Are you interested in being involved in a children's program for Oprah and work on the school issues, with help of course? Have you seen the two new ad hoc groups formed? The addresses are in message number 19225! We're meeting there now. Thank you so much, uma > hi uma! we love cats too :-) > > just wanted to make a little corrections here - the Guidelines For > Schools was put out by the Nat'l CFIDS Foundation (NCF), > http://www.ncf-net.org, not the CAA. > > i have about 20 of them right now. i ordered one for every school nurse > in the district. i was told just one in the district office was all > they needed. i still plan to distribute them in all the schools . .. Debbie > > in a couple states, i know that activists have been able to get grants > and have these sent to every school in the district. > > for those of you interested, there are several lists for activism out > there - CFIDS-L, me-activism@egroups, resact@egroups, there's more - > i'll dig them all up if somebody wants!!! > > <<< The CFIDS Association of America wrote a " Guideline for Schools " > regarding treatment of students with CFIDS which could be useful for > administrators, >>> > > ~~~~~~~~~~~~~~~~~~~~~~~~~ > " Quote Link to comment Share on other sites More sharing options...
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