hemophiliamom.com
Hemophilia Mom -
July 30, 2015. Well it’s that time of year Hemo Friends and by that I mean it’s almost School Time! Well, have a great rest of the summer and here’s to another school year! Relationships & Children with Special Needs. July 15, 2015. Okay so this blog is going to be a little touchy, it’s something that I’m currently going through and I’m sure other moms and dads are going through this too. As always, I will keep moving on like a hemophilia mom does. Time for School Already? July 10, 2015. That being said,...
hemophiliamoms.blogspot.com
Hemophilia Mom's Forum
A place for moms and other family members to discuss hemophilia. Saturday, September 22, 2012. Today is the day! I am in Dallas with 95 kids with a bleeding disorder who will compete today in Baseball and Golf! Let me know if you or your child is here! Wednesday, September 12, 2012. Junior National Championship Dallas. I am getting so excited to see all the families at the 2012 Junior National Championship in Dallas the weekend of September 21! Tuesday, July 31, 2012. Monday, May 14, 2012.
hemophilianc.org
Hemophilia of North Carolina
Since 1977, serving the people. Affected by bleeding disorders. 260 Town Hall Dr., Suite A, Morrisville, NC 27560. HNC tiene un número de teléfono gratuito para el grupo HNC Unión Latina y los miembros que hablan español:. En español solamente / sin cargo). HNC has a toll-free number for the HNC Latin Union group and Spanish speaking members. Follow us on Facebook! Hemophilia of North Carolina. Medical Advisory #423 – CSL Behring Discontinues Production and Distribution of Monoclate-P. Health Reform Upda...
hemophilianest.com
The Hemophilia Nest
Enter your Twitter name to be added to the nest. Subscribe to the nest. Get weekly email updates with the top tweets from the nest. Tweets from the past 1 day. About 2 years ago. I just want off work! About 2 years ago. Idiot Assemblyman John Wisniewski introduces bill to designate salt water taffy as NJ's state candy http:/ t.co/WpOW2TEz5h. About 2 years ago. Happy 10th Birthday to my baby girl! About 2 years ago. Share this community with your friends and family. Contributors add links to The Nest.
hemophilianevada.org
United by Hemophilia in Nevada :: http://www.hemophilianevada.org
United by Hemophilia in Nevada. Sticky: I Am Glad That I Finally Did Something Positive for My Back. As a young person, I had no problems with my back, just as many other young people do not. But I found out the hard way that various events and age can bring on issues, and this is why I found myself looking for a chiropractor in Alexandria VA. Laquo; Previous post. Title: Biogen to Give Poor Hemophiliacs Free Medicine. The company, which acknowledged the timing of the donation coincides with the launch o...
hemophilianewborn.com
Pediatric Hemophilia Study
Your personal experience could help shape clinical trials. Help Advance Medical Treatments for Hemophilia A. Hemophilia A is a rare, inherited bleeding disorder. Approximately 18,000 people in the US have hemophilia. And each year about 400 babies in the US are born with this disorder. Whether you are living with hemophilia A or caring for someone who is, you can make a difference today by taking part in a short survey. Your personal experiences with hemophilia may help shape clinical studies and tre...
hemophilianewborn.info
Pediatric Hemophilia Study
Help Advance Medical Treatments for Hemophilia A. Hemophilia A is a rare, inherited bleeding disorder. Approximately 18,000 people in the US have hemophilia. And each year about 400 babies in the US are born with this disorder. Clinical research studies are an important step in the development of new medicines. When medical conditions have few treatment options available or when breakthrough treatments are being tested, clinical trials become even more critical. This is the case with hemophilia A. Hemoph...
hemophilianewborn.net
Pediatric Hemophilia Study
Help Advance Medical Treatments for Hemophilia A. Hemophilia A is a rare, inherited bleeding disorder. Approximately 18,000 people in the US have hemophilia. And each year about 400 babies in the US are born with this disorder. Clinical research studies are an important step in the development of new medicines. When medical conditions have few treatment options available or when breakthrough treatments are being tested, clinical trials become even more critical. This is the case with hemophilia A. Hemoph...
hemophilianewborn.org
Pediatric Hemophilia Study
Help Advance Medical Treatments for Hemophilia A. Hemophilia A is a rare, inherited bleeding disorder. Approximately 18,000 people in the US have hemophilia. And each year about 400 babies in the US are born with this disorder. Clinical research studies are an important step in the development of new medicines. When medical conditions have few treatment options available or when breakthrough treatments are being tested, clinical trials become even more critical. This is the case with hemophilia A. Hemoph...
hemophilianw.ru
Всероссийское общество гемофилии. Северо-Западный федеральный округ.
Протокол "гемофилия" (.pdf). Новогоднее Шоу Снежная королева в Санкт-Петербурге. Школа ИТП в Санкт-Петербурге. В Санкт-Петербурге 23 декабря 2017г. в конференц зале НИИ гематологии и трансфузиологии состоялась «Школа иммунной тромбоцитопении (ИТП)». Поздравляем вас с наступающим Новым Годом и Рождеством! Пусть в нашем обществе - обществе ГЕМОФИЛИИ будут МИР, СЧАСТЬЕ и, конечно, ЗДОРОВЬЕ! Пусть сбудутся наши мечты в 2018 году! Новгородские Школы гемофилии - новый взгляд на вопрос.
