
If we could take away the SMS, we probably would, but despite all of the struggles our children face they amaze us every day with their curiosity, determination and humour. Such a joy and a blessing to have them in our lives!
Thank you for your time and support through our Sponsor our Smile campaign!
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Smith-Magenis Syndrome Fact 29
Additional support organizations in Germany and Denmark offer information for parents and caregivers. Visit these sites at:
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Smith-Magenis Syndrome Fact 28
There are a couple of newer foundations that have formed in the US over the last few years who are also dedicated to supporting SMS.
Smith-Magenis Syndrome Research Foundation.
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Smith-Magenis Syndrome Fact 27
ASM17 France
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Smith-Magenis Syndrome Fact 26
The Organisation that supports those is the UK is The Smith-Magenis Syndrome Foundation UK.

Smith-Magenis Syndrome UK Foundation
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Smith-Magenis Syndrome Fact 25
There are a few volunteer, parent-led organizations working to better the lives to those affected with SMS. These organizations do so many good things and we sincerely appreciate their hard work!
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