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ear tubes

United States

Zeegoner

New York, New York

Blogilates

California
Hello! I am a Pilates Instructor and a YouTube fitness guru who is crazy about living healthfully. I write about all things diet and fitness and am cooking up a ton of uber nutritious recipes daily. You can check out my blog at blogilates.com or workout with me on YouTube at youtube.com/blogilates where I instruct POP Pilates classes.

rachelh

California
I am a College student studying American Sign Language. My hobbies include Ballet and YouTube Makeup Tutorials. I have been dating my boyfriend for a year. 

Lynn Patient Expert

Chicago, Illinois
I am a former paramedic, former insurance claim investigator, and the mother of five!  My youngest has had many hospitalizations and medical emergencies.  She is fed by g-tube and I have become a specialist in g-tubes.  

Heather M.

United States
Carter was born on March 27, 2009. We were surprised to learn that he had a cleft lip/palate and was missing his right outer ear. Our little guy was whisked away to the NICU with breathing difficulties. A few days later he was transferred to the children's hospital which is one hour away. He spent the next 10 weeks there. During that time he was diagnosed with a Chromosomal disorder which...

eva

vlore, Albania
I am 30 years old...i am trying and trying to have a baby...but he seems tooooo far away...i have done 3 Fivet-no result,at october i'll do it again!!!I will never stop till i have a baby,cause all our parameters are very good.I have lost one of my fallopian tube and the other is blocked...pfffff...but i'm not tired!!!I want to be mom!

Kodi Wilson Facebook

United States
Well, we are no celebrities, just a family going through life and it's ups and downs with a special needs child. Our son is diagnosed with Leigh's Disease, a terminal degenerative disorder which is categorized as a mitochondrial disorder... as it eats away at muscle tissue and brain matter. He also has severe epilepsy, developmental delays, cerebral palsy, reflux, lives on a ventiltor and trach...
Communities: Children's Health

Hank Osborne

Goose Creek, South Carolina
I'm the father of Caden Gabriel Osborne (pictured). Caden born with 22q11.2 on 11/2/04 has endured numerous complications associated with a 22q11.2 chromosome deletion. His primary diagnosis is also called VCFS (Velo-Cardio-Facial Syndrome) or DiGeorge Syndrome. Caden's complications have included multiple heart defects, scoliosis, feeding difficulties, hypocalcemia, immune deficiencies, and...