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THIS SATURDAY – Join TSAOG As We Take One Small Step for Prader-Willi Research

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TSAOG’s Dr. Sergio Viroslav has a daughter with Prader-Willi Syndrome, so this cause is very close to his heart. He has agreed to share his personal story to help raise awareness:

We always felt something was amiss. This pregnancy was different than Alice’s prior one; fetal movement was sporadic and with less vigor. The ultrasound showed excessive amniotic fluid. At least the amniocentesis revealed the normal number of chromosomes.

One month to go, Alice was admitted to the hospital with a baby that wasn’t moving much; the OB had done all she could do in 1996. All we could do was wait for the lungs to mature and hope for the best.

Olivia was born 1/11/96. She weighed less than 6 lbs, her tone was low, but at least she was alive and eating.

She didn’t walk until she was three. Then this small infant who we were told had some sort of muscle or energy producing disorder began to gain weight. She didn’t particularly eat more than her siblings, though she did seem to care more about food then her older sister and younger brother.

In 2001 a visit to a childhood obesity clinic prompted the endocrinologist to check for Prader Willi Syndrome (PWS). The doctor told us not to worry. Olivia was engaging and bright. She was performing well at school, and the chromosome test was standard in working up obesity in children. We were cautiously optimistic.

As the Twin Towers were falling on September 11th we received the news. Olivia’s 15th paternal chromosome had a deletion – Prader Willi Syndrome.

Olivia is now a junior in high school. She plans to attend college when she graduates. She has friends and is active in her Temple youth group. But every day is a challenge. The pantry is locked in our home. She takes a daily shot of growth hormone to help her muscles and metabolism. She takes medicine to help her when she becomes fatigued and medicine to help her cells use insulin more efficiently. She is at the gym every day, she eats less than 1500Kcal and she can barely lose a pound. Her hunger never ceases.

That’s why we do this. We do this to help kids with Prader Willi . We do this because it’s the only way to fight. It’s the only way to find a cure. 

“ The greatest of all mistakes is to do nothing because you can only do a little – do what you can.”-  Sydney Smith

TSAOG will be collecting donations in our clinics (where you can purchase a pair of One Small Step cut-out feet for $2) and online to help the Foundation for Prader-Willi Research work towards a cure for Prader-Willi Syndrome. All donations will go to the Foundation for Prader-Willi Research (FPWR)

The fundraising for FPWR will culminate with a family friendly walk at the Tobin Center
 on Saturday, November 11th from 9am-11:30am.  Please join us at this fun, family friendly event to help raise awareness of this disease and contribute what you can to help work towards a cure. Register or donate here.

 

 


NOTE: We cannot provide medical advice or diagnoses without seeing a patient in person.

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