Our family has been deeply impacted by the challenges of pulmonary hypertension (PH) for over a decade. My mum has bravely battled this rare and often misunderstood disease, enduring its long-lasting effects.

When a person develops PH, the walls of the pulmonary arteries become stiff and thickened, or blocked by blood clots. This makes it difficult for them to expand; and trying to pump blood through these tightened, narrowed, scarred or blocked arteries puts increasing strain on the right side of the heart as it tries to do its job. The essential task of pumping blood into the lungs to pick up oxygen which can then be circulated to every cell in the body becomes much harder.

As we join hands with the Pulmonary Hypertension Association UK, we are driven by the shared goal of alleviating the burden faced by individuals like my mum. The PHA UK tirelessly provides support, guidance, and advocacy, striving to enhance the quality of life for those affected by PH. By raising awareness and funding crucial research, they aim to pioneer better treatments and ultimately find a cure for this devastating illness. It's important to note that the PHA UK relies solely on donations, as they receive no government funding.

Every contribution, no matter how small, plays a pivotal role in empowering individuals to lead better lives despite PH's challenges.

We are embarking on a personal trek up Ingleborough on May 25th, 2024 in support of the Pulmonary Hypertension Association UK. Our target is to raise £200 for this vital cause.

Your support will make a meaningful difference in the lives of those battling pulmonary hypertension. Together, let's bring hope and relief to individuals and families affected by this relentless disease.

Pulmonary Hypertension Association