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Join date: Jun 6, 2024
Posts (5)
Jul 21, 2026 ∙ 2 min
Hope Floats
When I was diagnosed with Pulmonary Hypertension in December 2018, I was too sick to try any other medicine than the IV pump. And though it saved my life and gifted me with a few more precious years, I can’t help but think about the circumstances that allowed for that solution to be sustainable, at least for a little while. I lived with someone. I had family close by. I had dexterity in my limbs and the mental function to handle the logistics of everything that came with the pump, including...
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Nov 24, 2025 ∙ 2 min
A Tag Team of Rare Disease Education by Kate Salonga
On Saturday, October 25th, I attended the Scleroderma Association of BC’s 2025 AGM and conference. For those unfamiliar - like myself a few weeks ago - scleroderma and pulmonary hypertension have a very interesting relationship, which is why PHA Canada usually has a booth set up at this annual meeting. Scleroderma is an autoimmune disease that causes hardening and/or thickening of the skin and internal organs. Sound familiar? That’s because scleroderma patients are at risk of developing PH ....
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Oct 8, 2025 ∙ 2 min
Breathless in Seattle
Kate Salonga represents PHA Canada at the 2025 PH Professional Network Symposium hosted by the Pulmonary Hypertension Association (US)....
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