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New CH.com Forum › Daily Chat › General Posts › Amounts of Cluster research vs. Tourett's research

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Amounts of Cluster research vs. Tourett's research (Read 908 times)

writer

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Amounts of Cluster research vs. Tourett's research
Oct 17^th, 2011 at 1:32pm

A cluster sufferer of 40 years, I find it interesting but sad that an estimated 200,000 Americans suffer from Tourette's syndrome, for which there is extensive, funded, ongoing government research-- while an estimated 1 million Americans suffer from cluster, for which there is little to no ongoing government research.

When will we gather our strength and mobilize to get the cluster research that is needed?

Writer

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Linda_Howell

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Re: Amounts of Cluster research vs. Tourett's research
Reply #1 - Oct 17^th, 2011 at 5:39pm

Quote:

Tourette's syndrome, for which there is extensive, funded, ongoing government research-

Can you produce a link to that effect so I (we) can read that?

We here, have always known that research and funding for CH will never take a high priority with scientists because of it's rarity and the absence of money for them to make on it. I don't know a lot about Tourettes sydrome so I would really like to read that ongoing Gov. research and funding for it.

Linda

Hurt people.....hurt people. Think about it.

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writer CH.com Junior Offline I love YaBB 1G - SP1! Posts: 64 x0\|Washington, D.C.\|USA\|\|0\|0\| Gender:	Re: Amounts of Cluster research vs. Tourett's research Reply #2 - Oct 18^th, 2011 at 12:40am Hi, Linda--I don't have the link handy, but if you Google Tourette's Syndrome, you'll get the info with no problem-- Writer
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seaworthy CH.com Hall of Famer Offline Posts: 706	Re: Amounts of Cluster research vs. Tourett's research Reply #3 - Oct 18^th, 2011 at 7:12am Quote: while an estimated 1 million Americans suffer from cluster Where did that estimate come from?
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deltadarlin CH.com Alumnus Offline I love YaBB 1G - SP1! Posts: 3823 Downsville LA Gender:	Re: Amounts of Cluster research vs. Tourett's research Reply #4 - Oct 18^th, 2011 at 8:01am I googled Tourettes' syndrome and the only thing I found was an $800,000.00 grant awarded in 2010.
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writer CH.com Junior Offline I love YaBB 1G - SP1! Posts: 64 x0\|Washington, D.C.\|USA\|\|0\|0\| Gender:	Re: Amounts of Cluster research vs. Tourett's research Reply #5 - Oct 18^th, 2011 at 1:22pm Linda et al, For Tourette info, see the Natl. Institute of Neurologic Disorders and Stroke, at Multimedia File Viewing and Clickable Links are available for Registered Members only!! You need to or ; Click on "What Research Is Being Done." Writer
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Potter CH.com Alumnus Offline Team MOOSE DROOL Stinky Stuff on a Hook Prostaff Posts: 3600 Blgs.Mt. Gender:	Re: Amounts of Cluster research vs. Tourett's research Reply #6 - Oct 18^th, 2011 at 1:25pm I DISAGREE my son-in-law has Tourettes and I wouldn't trade him ever. Ya shoulda picked the clap. Potter
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Kevin_M CH.com Sponsor Offline withered branches grow green again. Posts: 8754 Michigan, USA Gender:	Re: Amounts of Cluster research vs. Tourett's research Reply #7 - Oct 18^th, 2011 at 3:21pm seaworthy wrote on Oct 18^th, 2011 at 7:12am: Quote: while an estimated 1 million Americans suffer from cluster Where did that estimate come from? U.S. 312,447,583 (population) 19:13 UTC (EST+5) Oct 18, 2011 Yeah, 1 in 312 seems high.
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