Wednesday, May 05, 2010

The Ross Sisters

This has been circulating around the net lately. Kind of lame at first but it gets better. Amazing, actually.

11 comments:

srinivas said...

Amazing video indeed. Wonder if all three suffer from Ehlers Danlos syndrome.

Crystal Nagy said...

No, they did not. they were not physically nor mentally ill. I am the Granddaughter of Betsy Ann Ross so I would know...If you have any other questions I would be pleased to be asked them.

Anonymous said...

Crystal, My father was an Army Air Corp Pilot with Robert Hightower. They were good friends while in Smyra, TN. My father is still living @ 92. Would love to get in contact with you!

Anonymous said...

Crystal,
There is no...or at least should be no...stigma attached to having Ehlers-Danlos Syndrome. It is certainly not a mental illness. A very few lucky ones don't even realize they have it until significant joint pain later in life. If your grandmother and grand aunts lived past 60 and didn't suffer pain, that's great; they probably didn't have it. But there's no need to be defensive about the inquiry. Lots of smart, competent, and graceful people have EDS; unfortunately, we don't get to stay mobile very long past our 40's.

zebra said...

As this video is circulating around Facebook, everyone in the Ehlers-Danlos forums are thinking they have it. A lot of us are just as flexible. (takes one to know one sort of thing). Were just curious how their joints held out later in life when they weren't so active. Their muscle tone probably helped.... Many people have this condition, but it goes undiagnosed. Flexibility is just one sign of it. It's genic so if anyone in this family has any medical issues, they might want to look into it.

Just saying....

Anonymous said...

Are any of them still living? What was thier quality of life after 40 ...Eds is not a mental issue and most ppl dont know they have it. Im sure back then it would have have been a diagnosis that ppl got. Im 34 and can still do the things they did in the video. Its not good for those of us to do with EDS but I just got diagnosed a yr ago before that I had never heard of EDS and didnt know that the things I can do where from EDS I thought it perfectly normal for ppl who stretched. I would place my money on EDS...is any of their off springs flexible?

Anonymous said...

My daughter has EDS. The very first thing I thought when I saw this video was EDS

Anonymous said...

My husband, his brother and their mother passed away from aortic aneurysms. Last year a doctor determined that my daughter has EDS based that on how flexible her joints are. There are different forms/levels of EDS but I think joint flexibility is the common denominator. I pray to God everyday for a treatment or cure.

Unknown said...

Seeing that the youngest sister killed herself at 33, and there's no such thing as double jointedness, yes. This family was on the Hypermobility Spectrum and most likely never realized.

Unknown said...

No one suggested they were mentally ill. From what I understand, ehlers danlos syndrome is super flexibility of the skin and joints. Most people cannot do what they could

Anonymous said...

My son can bend his fingers backwards and touch his wrists. My wife can touch her toes to the top of her foot or bend her whole foot backwards and touch her toes to her shins. I wonder if they have it. I'd never heard of EDS. My son gets tired walking because he has to use muscles because his ligaments don't stop the motion or give spring like most of us. I need to look into this. Thanks.