Aug 30, 2022
Pulmonary hypertension patient, Larissa Domenichelli discusses her rare disease diagnosis and why she feels like a 73 year old trapped in a 37 year old's body.
My name is Larissa Domenichelli. I'm from Cloverdale, California. My connection with pulmonary hypertension is I was diagnosed in November of 2020. I was in...
Aug 29, 2022
In this episode, pulmonary hypertension patient, Larissa Domenichelli discusses her rare disease diagnosis and why she feels like a 73 year old trapped in a 37 year old's body.
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Aug 23, 2022
Pulmonary hypertension patient, Tina Gardner had never heard of PH when her mom was diagnosed in 1994. 28 years later, she's all too familiar with the disease after she, her nephew, her niece as well as her great nephew have been diagnosed with this rare disease. Tina discusses the importance of support...
Aug 22, 2022
Pulmonary hypertension patient, Tina Gardner had never heard of PH when her mom was diagnosed in 1994. 28 years later, she's all too familiar with the disease after she, her nephew, her niece as well as her great nephew have been diagnosed with this rare disease. In this episode, Tina talks about the importance...
Aug 16, 2022
Pulmonary hypertension patient, Nicole Hogan was diagnosed in 2018. Four years later she is still grappling with her rare disease prognosis. PH has changed her life. Now she advocates for herself and the community to help make PH history.
My name is Nicole Hogan, and I'm from San Fernando Valley. I was diagnosed with...