TOPIC:

I can not find anything concerning GILLES DE LA TOURETTE:

Anyone?

My e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

I'm going to include the first part of the wikipedia description here, for those who don't know it.

There are a couple of things I note that may be significant: It states that it's an inherited neuropsychiatric disorder - but it also states that the exact cause is unknown.

We know that MMS (and CDS) work on pathogens -
We also know that some autistic children have tics that resolve -
We are finding, through Kerri Rivera's work that a LOT of autistic children have parasites -
We are also finding, through Dr. Simon Yu's work in Bolivia, as well as our own Andreas Kalcker's work and research, that there's a lot of undiagnosed parasite infestation in the general population.

If GTS is simply an inherited neuropsychiatric disorder (it's a syndrome) - then MMS will probably not help.

IF GTS is actually the result of parasites, then MMS (and possibly the addition of a parasite protocol) will help.

Tourette syndrome (also called Tourette's syndrome, Tourette's disorder, Gilles de la Tourette syndrome, GTS or, more commonly, simply Tourette's or TS) is an inherited neuropsychiatric disorder with onset in childhood, characterized by multiple physical (motor) tics and at least one vocal (phonic) tic. These tics characteristically wax and wane, can be suppressed temporarily, and are preceded by a premonitory urge. Tourette's is defined as part of a spectrum of tic disorders, which includes transient and chronic tics.
Tourette's was once considered a rare and bizarre syndrome, most often associated with the exclamation of obscene words or socially inappropriate and derogatory remarks (coprolalia), but this symptom is present in only a small minority of people with Tourette's.[1] Tourette's is no longer considered a rare condition, but it is not always correctly identified because most cases are mild and the severity of tics decreases for most children as they pass through adolescence. Between 0.4% and 3.8% of children ages 5 to 18 may have Tourette's;[2] the prevalence of transient and chronic tics in school-age children is higher, with the more common tics of eye blinking, coughing, throat clearing, sniffing, and facial movements. Extreme Tourette's in adulthood is a rarity, and Tourette's does not adversely affect intelligence or life expectancy.
Genetic and environmental factors play a role in the etiology of Tourette's, but the exact causes are unknown........

Hi Pam,

I've read your information, bit it is not clear whether MMS ( MMS1 or MMS2 ?? ) should be taken to take care of Gilles de la Tourette.

You think MMS will help out?

Awaiting your reply, I remain with my best regards,

Frans

Frans, it depends on the cause of the disorder. If it is pathogen based, MMS will help. If it is not pathogen based, then MMS will not help.

Personally, I would do a full parasite protocol, with MMS1 as a supplement, and expect to do it for about 6 months (or longer). But, I'm guessing here - this is not a Jim Humble recommended protocol.

Hi Pam,

I thank you for your help:

A friend of mine is trying to find a way to deal with his "illness" although he did tell me that he has been feeling much better since he was able to loose 10 kilos and did so by juicing.
I've been taking MMS1 and 2 for various complaints and I know that the stuff works.
I will inform my friend and will get back to you and the forum as to how MMS works on Gilles de la Tourette.
Thanks for your input and help!

Best regards,

Frans van der Heijde, Netherlands