A video glimpsing into the lives of those who live with eosinophilic disorders, people who are helped by the CURED (Campaign Urging Research of Eosinophilic Disorders) Foundation. For more informat...
A video glimpsing into the lives of those who live with eosinophilic disorders, people who are helped by the CURED (Campaign Urging Research of Eosinophilic Disorders) Foundation. For more information visit www.curedfoundation.org !!
Like to rate videos and let people know what you think?
Automatically share your ratings, favorites, and more on Facebook, Twitter, and Google Reader with YouTube Autoshare.
Autoshare makes certain YouTube activities public on the services you choose. Select only the services you are comfortable with - like Facebook, Twitter, or Google Reader - to let your friends know what you like on YouTube. You can turn Autoshare off at any time.
Like to share videos with friends?
Automatically share your ratings, favorites, and more on Facebook, Twitter, and Google Reader with YouTube Autoshare.
Autoshare makes certain YouTube activities public on the services you choose. Select only the services you are comfortable with - like Facebook, Twitter, or Google Reader - to let your friends know what you like on YouTube. You can turn Autoshare off at any time.
my little boy thomas has eosinophilic collitus i thought i was on my own thank you for letting me know im not .The cakes of ice made me cry so much this is our life god bless all who have to enter this world in pain !!!!i love my boy please find a cure and make him better his mum Lisa x
Hi Lisa, I am English (living in Arizona). Been here 11 years. My 8 year old has EE (esophagus). I have the luxury of having UK and US doctor advice. Must admit US is more advanced. We have a strong support group, I feel very blessed. I've met kids younger and older with this disease. They are AMAZING! My heroes. Email anytime...we are going to Great Ormond St in summer next year...
I have Hyper EE. Mine first started when I was 28, I am currently 32. I am treated by The Mayo Clinic in Rochester. If you have any questions please feel free to message me and I will do my best to help as I have extensively dealt with EE first hand.
I am a teenager with both EE and recently diagnosed Eosinophilic gastroenterits that was misdiagnosed as crohns. docters are still puzzled some of complications i have suffured and are started to suspect that i may also have HES. life with a horrible stomach sucks. this video does a great job showing that.
thankyou for sharing this wonderful video...my 4yr old son has eosinophilic colitis thankfully he is in remisson..unfortunatly here in uk there is very little info on it and noone you speak to has even heard of it...
This is a wonderful video. I was wondering about eosinophilia in the blood because mom has a lot of eosinophilia in her blood. Something like 1400 in her blood and the maximum was 500 and the the doctor never said nothing to her about it. I was curious so I thought I would do my own research on it.
My 2 1/2 year old has Eosinophil Colitis and was diagnosed at 15 months. he is in remission now and we are thankful for every day. This video has helped up share what life is like with this disease to our friends and family. Thank you!
I have this disease and this is probably the most amazing video ive ever seen on youtube , not only about these disorders , but period. Thank you for it
Autoshare makes certain YouTube activities public on the services you choose. Select only the services you are comfortable with - like Facebook, Twitter, or Google Reader - to let your friends know what you like on YouTube. You can turn Autoshare off at any time.