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HEMOPHILIA FOUNDATION OF ILLINOIS

 

 
 
 

The Hemophilia Foundation of Illinois is an organization dedicated to improving the quality of life for persons affected by hemophilia and other inherited bleeding disorders, and complications of these disorders or their treatment.

 

The Hemophilia Foundation of Illinois provides and promotes Advocacy, Consumer Services, Education and Research. We are a not-for-profit 501(c)(3) organization and members of the National Hemophilia Foundation, the Hemophilia Federation of America, and Community Health Charities.


GIVE US YOUR FEEDBACK!

Click here to give us your feedback for the
2012 Statewide Fun & Education Weekend

 
BRADLEY KRUEGER MEMORIAL SCHOLARSHIP NOW AVAILABLE!

Click here to learn more about this Scholarship
and many more on our Scholarship Page!

 

CAMP WARREN JYRCH
APPLICATIONS AVAILABLE!

Camper Application
New Staff Application
Returning Staff Application


REP. MICHELLE MUSSMAN HOSTS
COMMUNITY FORUM
TO ADDRESS
ACCESS
TO SPECIALITY MEDICATIONS, RISING CO-INSURANCE

Local Posting on the TribLocal Schaumburg
 

IMPORTANT INFORMATION
FOR ADULT MEDICAID PATIENTS

Important information regarding the changes as the State of Illinois moves towards the  managed-care model "Integrate Care Program".
 

NEWLY DIAGNOSED?

Were you or a family member just diagnosed with a bleeding disorder?  We can help, Click here to learn how!

HELP US SHAPE THE FUTURE! 

Take our quick survey today to help us serve the Illinois bleeding disorders community better!

Click here to get started! 

 

DRIVING fore HEMOPHILIA

Please Join Us for the 15th Annual DRIVING fore HEMOPHILIA Golf Event Benefiting Children and Adults with Inherited Bleeding Disorders!

This event is a tremendous opportunity to come together to raise vital support that helps children and adults with hemophilia and other inherited bleeding disorders to live strong productive lives by having access to the critical programs provided by the Bleeding Disorders Alliance Illinois.

Click here to learn more!
Contact Bob Robinson to reserve your spot today!

 

WORD FROM THE DIRECTOR

 

Click here to read Bob's Hot Button Message

 

 

 

 

SPRING 2012 FACTORNET

Read it now - Here!

 

 

 

 

 

 

 

 

EVENTS & CONFERENCES

Check here often to find out more information about our events!

 

 


 

 

 

 

 

 

 

        

 

Read Laurie Kelley's new blog!

Laurie is the mother of a child with hemophilia, and founded LA Kelley Communications, Inc. in 1990 to provide practical educational materials for families.

 

Novel Approaches to
Bleeding Disorder Treatment

Health Insurance Reform

Bad Blood Documentary Article from PEN

 

Hemophilia Emergency Care

 

Atencion de Emergencia para la Hemofilia

 

A site designed to assist you when seeking care in emergency rooms or treatment facilities aside from your Hemophilia Treatment Center. www.hemophiliaemergencycare.com

   210 S. DesPlaines St.
  Chicago, IL 60661-5500
  Telephone:
  312.427.1495
  Fax: 312.427.1602
  E-mail:
info@hfi-il.org

 
If you have suggestions for improvements,
email us at:
info@hfi-il.org

By clicking on the links to the left, you will be taken off the HFI website and as such, HFI cannot be responsible for the content.

 

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