Not sure who or what PHA-UK are or do... click here to find out more! They are a small charity, but have the biggest heart - literally! They do so much for those with and who care for us PH'ers! All the money they use is from the donations of their supporters. They are not government funded, but they fight tooth and nail to support us and get the treatment we need! Please help support them and have a read of all the great things that they do - Thank you!
My husband and I attended the PHA UK conference! It was my 2nd conference and Terry's first! We both learnt a lot about my heart condition, Pulmonary Hypertension, especially Terry. However I also learnt new things about PH and hearing about future medications and technologies that will keep me and my Friends keep our hope of a future cure! Whilst we are there to learn more about our condition, it is also gives us all a chance to socialise and become friends with people who also suffer with PH. #NoCureAlwaysHope
The Pulmonary Hypertension Association UK ran such an incredible conference held at the beautiful hotel of Crowne Plaza in Oxford. They had such great speakers, who were all confident and full of knowledge in their own expertise. The seminars after the conference were great, with me and Terry trying out Tai Chi!! It was fun and a good laugh! The night ended with the gala ball, where many dressed up as Pirates! The food was delicious and with the dance floor lit up, Terry and I with many others danced the night away!
Congratulations PHA-UK for such a successful conference, and we look forward to the next one!!
Thanks for reading!