Williams Syndrome on Facebook

Causes on Facebook | Williams syndrome

Support for non-disabled siblings

Support for non-disabled siblings - 3/19/09 - Chicago News - abc7chicago.com:

"March 19, 2009 (CHICAGO) (WLS) -- Having a sibling with a disability is not always easy. Many need a support network to share their experiences.

It's bowling night for teens from Illinois Masonic hospital's Sibshop.

'It's really about enjoying each other 's company, celebrating the good things as well as maybe talking bout some of the difficult things that come about when you have a brother or a sister with a disability,' said Coordinator Sheila Swann Guerrero.

Guerrero says Sibshops has been a supportive network for non-disabled siblings for 20 years.

'They might not get the same amount of time with their parents as they would like to have, and often in our sib groups, giving children the opportunity to express that and then hear that other brothers an sisters are experiencing the same thing kind of gives them the green light that it's ok.'

Sixteen-year-old John Dahlstrom has been involved with Sibshop for many years. His older sister has Williams syndrome."

Brendan Lemieux - A Williams Syndrome Drummer

Brendan Lemieux: Rare Talent - The Source:

"You may still have plenty of time to become a prodigy if you’ve taken your first steps before you make your first foray into music, but Brendan Lemieux will have gotten the jump on you.

Brendan, now 21, was whistling Beethoven before he could walk.

“My mom told me that I was whistling at 14 months,” says Brendan, who picked up a pair of drumsticks at age three and has been playing ever since.

The motivation behind his proficiency is also unique. Brendan, who has the rare genetic condition Williams syndrome, suffered from the sensitivity to loud noises that often accompanies this disorder. Although it might seem paradoxical, playing the drums helped him overcome the physical illness that used to accompany loud noises.

While there is no doubt that Williams syndrome has its downside, including heart defects and joint problems, Brendan’s heightened sociability and musical abilities also result from the disorder."

Medical News: Microdeletions in IVF Embryos Caught With New Diagnostic Technique - in Endocrinology, Infertility from MedPage Today

Medical News: Microdeletions in IVF Embryos Caught With New Diagnostic Technique - in Endocrinology, Infertility from MedPage Today:

"Duchenne and Becker muscular dystrophy, Prader-Willi syndrome, and Williams syndrome are some of the disorders believed to result from microdeletions. FISH methods can also detect copy-number variations that underlie a range of other genetic diseases.

FISH methods use nucleotide probes that hybridize with target sequences, tagged with a fluorescent molecule so that successful binding can be visualized under a microscope.

For detecting microdeletions in a particular gene, the probe is designed to bind its normal sequence. An absent fluorescent signal indicates that hybridization failed, meaning the gene is missing or defective.

FISH is a standard laboratory tool for cytogenetic analysis, but its adaptation to in vitro fertilization (IVF) embryo analysis is relatively untested, in part because it must be made to work on one or two cells.

In the current study, Dr. Vermeesch and colleagues used the technique on embryos from three couples having a total of seven IVF cycles. The women in these couples were known carriers of microdeletions related to neurofibromatosis type 1 or Von Hippel-Landau disease.

The researchers biopsied 64 embryos produced from these cycles. Two blastomeres with excised from each embryo for analysis. Although it would have been possible to perform the tests on single blastomeres, Dr. Vermeesch and colleagues believed analyzing two would be more accurate.

Incomplete results were obtained for 14 embryos and were excluded. The FISH procedure failed in one case, and only one blastomere could be analyzed in 13.

Of the 50 embryos successfully analyzed, 17 appeared normal and healthy. Deletions related to neurofibromatosis type 1 or Von Hippel-Landau disease were found in 27 embryos. The remaining embryos were mosaic or had other abnormalities such as copy-number variations.

Ten embryos were implanted in the women, two of which resulted in pregnancy -- twins born to one woman, with both infants found to be free of microdeletions.

Dr. Vermeesch and colleagues called the approach a success, but suggested it would be more practical when it can be implemented on an array platform. This technology would allow many different analyses for microdeletions and other mutations to be performed simultaneously."

The obvious ethical question is whether or not parents would abort the child if they discovered she had WS.

Friends, fun in Down Syndrome Association Soccer League

Friends, fun in Down Syndrome Association Soccer League | Jacksonville.com:

"Alex, 16, has a rare gene disorder known as Williams syndrome, which is marked by heart and vascular problems as well as extreme gregariousness - easy to see in the boisterous teen, ringleader of the noogie patrol.

During the game, Alex hurtles his body after the ball, tracking it like a lion after an antelope. For years he watched his brother and sister compete in their sports. Now it's his chance.

'We've got to watch his heart,' says his father. 'But the doctor said, 'Let him be a boy. He's got to be a boy.' '

And he is."

Family Looks for Help in Building Addition Onto Home for WS Son

CBS 7 - Your Eye on West Texas

Trace sufferes from Williams Syndrome, a genetic disorder which formed his arteries too small; making it difficult to breath and even harder to play.

"We're supposed to limit his activity and its hard to do with having older brothers and wanting to play and stuff."

The Covington's home is also a challenge. Trace doesn't have a bedroom and in between playing the piano and riding piggy back on his big brother's bike, Trace has few places to recoup.

"We're just wanting to have an environment so he can go and have fun instead of going outside and running and playing and stuff."

So, Trace's parents contacted the Make A Wish Foundation, in hopes of giving their son his first bedroom.

"It tears at our hearts that he's having to do without."

Unfortunately, just when they thought Trace's wish was granted, Make A Wish informed them otherwise.

Williams Syndrome Video Channel

MySpaceTV Videos: Williams Syndrome Video Channel

The Faces of Williams Syndrome - Video

New book chronicles family's challenges raising daughter with Williams Syndrome

Community Press - Book chronicles family's challenges:

"'Another Day, Another Challenge,' Strebe's first published work, is the story of a girl with Williams Syndrome and the story of a family that dealt with the challenges - it is the story of Strebe's youngest daughter Michelle."

Dealing with Other People's Expectations

Erik Quinn: The Heart of a Family: Minimize:

Nancy writes and expresses some of the frustration felt by parents of kids with WS:

"Sometimes I get the impression that people think I am making this entire WS thing up.

All of it.

These days I focus on the positive while being fully aware of WS, and perhaps that is confusing to others. Perhaps that makes Erik's disability disappear to them. Unfortunately, perhaps the hard work we have done to help Erik achieve each milestone and Erik's daily struggles also disappear in their eyes."