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Hemophilia Foundation of Illinois

 
 
Bleeding Disorders
Programs & Services
About HFI
 

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.

 

HFI  Relocating Offices

We also have big news to announce.  In celebration of our 60th Year the Board of Directors has decided to purchase a new home for the Hemophilia Foundation of Illinois corporate headquarters.  We have purchases a corporate space at 210 S. DesPlaines in Chicago.  Posted below is a link with basic information on the site and some early pictures.  We will continue to keep the community apprised of this process as the year moves on.  We anticipate moving some time in the fall or early winter. 

210 S. DesPlaines - HFI's New FutureHome

 

SPECIAL NOTICES - CAMP APPS AVAILABLE

 

Calling all campers for Camp Warren Jyrch 2009
being held from Sunday, July 26 to August 1, 2009.  Camp is being held at the Timber Pointe Outdoor Centre in Hudson, Illinois - the same location as last year.  All staff will need to report on
Friday, July 24.

 

Camper Application - Application Link - 6/13/2009
 

Counselor in Training Application - Application Link - 6/13/2009
 

Staff Application - Application Link - 5/30/2009

 

SPECIAL NOTICES - NHF ANNUAL MEETING TRAVEL GRANT APPLICATIONS AVAILABLE

 

The National Hemophilia Foundation is pleased to offer Educational Participant Grants for first-time attendees to its 61st Annual Meeting, “Building Bridges,” in San Francisco, California, October 29-31, 2009. In our quest to foster a more inclusive annual meeting, NHF offers a limited number of Educational Participant Grants to individuals and/or families with bleeding disorders attending the Annual Meeting for the first time.  We would especially like to provide assistance to those unable to attend due to personal obstacles or other barriers.  Awards will be based on these factors, as well as on need.  Grants may be used to cover airfare, hotel, related expenses and registration fees.  Applicants may apply for grants in one or more of these categories, for a maximum of three nights and four days. 
Applications must be postmarked by
Friday, June 26, 2009

 

Travel Grant Application

 
 

 

Spring 2009

 

 

FactorNet & Hot Button

 

Look for it in the mail - April 2009

Read it now - Here!

 

 

June 24, 2009

THE ILLINOIS DOOMSDAY BUDGET SITUATION

This week the Governor has convinced leaders of the General Assembly to come back into special session.  The Governor's office believes the state legislature did not give him a balanced budget.  The President of the Senate, Senator Cullerton, and the Speaker of the House, Representative Madigan, believes they have.  The bottom line is that at the current time we have a high level political game of chicken on the state level. 

The sad part is that the leadership is using health and behavioral health programs as their own props – including the Illinois State Hemophilia Program.  This is very disheartening, placing many vulnerable people in an even more state of heightened anxiety not how they and/or their family member are going to access the vital health care services necessary to live. 

A little more background before we provide any advice on strategies to become involved in this situation. The Governor’s office has communicated that they are mandated to operate the state with a balanced budget.  The Governor’s office has let it be known that if the 50% budget currently on the table is to be implemented they will massively cut health/social services in the state.  We have been informed this includes cutting the entire State Hemophilia Program.  This program pays for factor and comprehensive treatment visits for 250 – 300 people with bleeding disorders in Illinois each year.

Senator Cullerton and Representative Madigan believe they have given the Governor a balanced budget; since they gave him authorization to run the previous year's budget for the next six months.  This is being done because if there is to be a tax increase they want to vote on this after the Primary Election petitions have been filed in the fall.  Also, when the General Assembly goes into session in January 1 they only need a simple majority to pass the budget.  Currently, they need a 2/3 majority to do this which requires the support of the minority party.

There is tremendous public pressure mounting to get a budget adopted by July 1 -- the statutory start to the FY 2010 fiscal year.  The Governor and similar minded individuals have ramped up the voices of needing a budget with a tax increase in hopes of passing a budget by July 1 or shortly thereafter (legislature has used the deadline of first pay day for employees as a deadline when they've missed July 1).  The Leaders of the General Assembly have been very quiet because they are satisfied with the solution they have already delivered.

This is a critical time for our voices to be heard.  We need to do our best to contact our elected officials and tell them our Program and the full-range of human services for the state are vitally important.  When you do make these telephone calls (we do not have time to write) identify how you are directly connected to the bleeding disorder community and share your personal story.  Also, don’t forget to let them know that you are a constituent – actually one of his/her bosses.

We will keep you formed as this moves to a resolution.  If there is a compromise I am still anticipating that there may be changes to our program funding.  We will have to make adjustments and plans for how we are going to adapt to this.  If there is not a compromise, then it will be a completely different situation which we are already outlining how to approach. 

Bottom line, today, we all need to express our appreciation to the administration and legislature for the support of the Hemophilia Assistance Program since 1972 and note it needs to be continued.  Keeping Hemophilia in their minds is a very good call.

Bob Robinson
Executive Director 


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.


Hemophilia Emergency Care

 

Atencion de Emergencia para la Hemofilia

 

www.hemophiliaemergencycare.com

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

 

332 S. Michigan Avenue, Suite 1135
Chicago, IL 60604-4305
Telephone: 312.427.1495
Fax: 312.427.1602
E-mail:
info@hfi-il.org

National Hemophilia Foundation
NHF
Hemophilia Federation of America Community Health Charities of Illinois

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

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

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