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HHT: Diagnosis, Treatment and Management (Clinician Conference)

Chicago, IL

HHT: Diagnosis, Treatment and Management (Clinician...

Ticket Information

Ticket Type Price Fee Quantity
Friday Session ONLY - MANDATORY   more info $225.00 $0.00
Friday and Saturday Sessions - OPTIONAL   more info $375.00 $0.00
Friday, Saturday, Sunday Sessions - OPTIONAL   more info $425.00 $0.00
Saturday Evening Dinner / Auction   more info $75.00 $0.00
Raffle Tickets   more info
Scholarship Fund Donation   more info
HHT Foundation Membership $55.00 $0.00
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Event Details

You can impact the lives of thousands by attending this important educational activity jointly sponsored by the Northwestern University Feinberg School of Medicine and the HHT Foundation!

Do you have patients that suffer from nosebleeds, shortness of breath, fatique? Are any of your patients iron infusion or blood transfusion dependent? Is their a family history of nosebleeds, stroke, premature death? If so, this conference is for YOU!

This program is designed for medical professionals  who are likely to encounter HHT patients, among them: internal medicine, gastroenterology, otolaryngology, pulmonology, neurology, cardiology, interventional radiology, genetic counseling, or nursing. Nothwestern University Feinberg School of Medicine designates this educational activity for a maximum of 7.5 AMA PRA Category 1 Credit(s)TM. Physicians should only claim credit commensurate with the extent of their participation in the activity.

  • Most current information on HHT research, diagnosis, management, and treatment
  • Talk one-on-one with leaders in the field of HHT.
  • 16 workshops and presentations to choose from, including but not limited to: Consensus Guidelines for Management of HHT; Management of Pulmonary and Cerebral AVM; HHT Diagnosis, Treatment and Management in Children; Management of Gastrointestinal and Liver AVM; Management of Anemia; Medical Treatment and Management of Epistaxis in Adults and Children; Genetics of HHT; Inspiring Research Advances and Opportunities
  • The recently enacted Genetic Information Non-Discrimination Act (GINA) will be presented by the Acting Director of the National Human Genome Research Institute of the National Institutes of Health (NIH). This ground breaking law is important to everyone with a genetic disorder!

You also have the option of attending the Patient and Family Conference on Saturday and Sunday in order to learn more about HHT and interact with people affected by this disorder. 

We look forward to seeing you in Chicago . . .

Where


Hyatt Regency McCormick Place
2233 S. Martin Luther King Drive
Chicago, IL 60616

Hosted By

HHT Foundation International, Inc.



HHT Foundation International is a worldwide, non-profit organization whose purpose is to support patients and families and educate medical professionals. We are dedicated to the individuals and medical professionals who encounter the daily challenges of managing Hereditary Hemorrhagic Telangiectasia (HHT) also known as Osler-Weber-Rendu Syndrome.