Please help me support Cure HHT during June HHT Awareness Month by making a donation through my page. The process is fast, easy and secure. Thank you so much for your support! Please don't forget to share this page with any family or friends who might be interested in donating to a great cause.

About HHT:  Hereditary Hemorrhagic Telangiectasia (HHT) is a rare, inherited disease that affects over 1.4 million people worldwide (1 in 5,000) yet only 10% are actually diagnosed. 

It is caused by defective blood vessels in the brain, lungs, liver, nose, skin, and intestines, and typically begins with nosebleeds during childhood.  The most common symptom is uncontrollable nosebleeds. HHT is highly treatable but can result in life-threatening health problems if not promptly diagnosed and treated. 

90% of people with HHT remain undiagnosed which is why spreading awareness is so important. Many are commonly misdiagnosed with other conditions and wait on average approximately 27 years for a proper diagnosis of HHT. Your donation could help save a life!

About Cure HHT: Cure HHT's mission is to find a cure for HHT while saving the lives and improving the well-being of individuals and families affected by HHT. You can visit their website at:  www.CureHHT.org