NI Woman Battles Rare Condition, Loses Pints of Blood Daily

A 55-year-old woman from Carrickfergus, Northern Ireland, is raising awareness about her battle with a rare genetic disorder that causes her to lose significant amounts of blood daily. Sharon Gregg has been diagnosed with Hereditary Haemorrhagic Telangiectasia (HHT), a condition that leads to frequent bleeding from various parts of her body, including her nose, ears, eyes, throat, and even her stomach and bowels.

The impact of HHT on Sharon’s life has been profound. She experiences numerous bleeding episodes each day, resulting in the need for multiple blood transfusions. “I’ve had so many transfusions I’ve lost count,” she stated, highlighting the severity of her situation. The disease, which affects blood vessel formation, can lead to life-threatening hemorrhages if not managed properly.

Understanding Hereditary Haemorrhagic Telangiectasia

HHT is a genetic disorder that affects blood vessels, causing them to form abnormally. This condition can lead to spontaneous bleeding in various organs and tissues. Sharon believes that her family history suggests that her late brother, father, and grandfather may have also suffered from this condition, though it went undiagnosed during their lifetimes.

As a former hairdresser, Sharon’s daily life has been significantly altered by her health challenges. Simple tasks have become difficult, and she often finds herself in emergency situations due to unexpected bleeding. The need for blood transfusions has made her reliant on healthcare services, which she credits with saving her life on numerous occasions.

In sharing her story, Sharon aims to educate others about HHT and its implications. She hopes that increased awareness will lead to better understanding and management of the condition, as well as improved support for those affected.

The Importance of Awareness and Support

Raising awareness is crucial, especially for conditions like HHT that may not be widely recognized. Sharon advocates for more research and funding to improve treatment options and support for patients. She emphasizes the importance of early diagnosis and intervention, which can significantly enhance the quality of life for those affected.

Sharon’s determination to live life to the fullest despite her challenges serves as an inspiration to others facing similar health issues. Her story shines a light on the struggles of those with rare conditions and the vital role of community support in navigating such difficulties.

For anyone experiencing unexplained bleeding or other related symptoms, Sharon encourages seeking medical advice, as early detection can lead to better outcomes. By sharing her journey, she hopes to foster compassion and understanding for individuals living with HHT and similar disorders.