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PHA UK

@PHA_UK

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We are the Pulmonary Hypertension Association UK (PHA UK) - dedicated to supporting people affected by pulmonary hypertension.

Sheffield, England
Joined January 2010
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@PHA_UK
PHA UK
2 months
PH Day UK is back! Lets raise the profile of #pulmonaryhypertension together on Friday 7th November. All the ways to get involved: https://t.co/qcjdBX3CBv 📢 This year’s theme is #BreathlessNotVoiceless - will you help us turn up the volume?
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@PHA_UK
PHA UK
4 hours
Big thanks to the PH team at Royal Papworth Hospital for supporting #PHDayUK with an information stand and fundraiser this week 💜 A great job as always!
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@PHA_UK
PHA UK
7 hours
We're making it easier than ever to support #PHDayUK on your social media channels! You'll find a range of downloadable graphics and template text for posts at https://t.co/UXFVzdWZ3W. 🤳 Don't forget the selfies with our photo cards too!
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@PHA_UK
PHA UK
1 day
PH Day UK takes place THIS FRIDAY! Are you ready? Here's a reminder of all the ways you can get involved: https://t.co/fIg4AykUTL #BretahlessNotVoiceless
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@PHA_UK
PHA UK
5 days
🎬 The Right Heart Catheter is known as the 'gold standard' test for diagnosing PH and in this short video, we spoke to Dr Charlie Elliot - who has performed hundreds of these procedures - to answer common questions and concerns: https://t.co/pmhAAMgagN
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@PHA_UK
PHA UK
6 days
New PHA UK merchandise! Wear these unisex neck covers / multiway wraps in any way you like... Pull up over your mouth and nose to ease breathlessness when it’s cold, or wear as a hood, hairband, or scrunchie: https://t.co/CJBCqVbqin
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@PHA_UK
PHA UK
7 days
This new group is designed to help guide service development and research in paediatric PH, ensuring young voices are heard. The online meeting was followed by another with parents and guardians, and it was equally as valuable.
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@PHA_UK
PHA UK
7 days
Our first group meeting with youngsters with PH and the team from Great Ormond Street Children's Hospital took place yesterday, and it was great to hear all the feedback and ideas 💭 Find out more & get involved in future sessions: https://t.co/3IBeC24sfk
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@PHA_UK
PHA UK
8 days
We're delighted to be presenting 3 research abstracts, covering some important studies and bringing UK patient voices to this global gathering in January 🍀
@PVRI
The Pulmonary Vascular Research Institute
25 days
☘️ Dublin awaits! Hear from Seán Gaine, Scientific Organising Committee Lead for PVRI 2026, as he shares why next year’s Congress in Dublin will be one to remember — celebrating 20 years of PVRI and the incredible progress in pulmonary vascular science and care. PVRI 2026
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@PHA_UK
PHA UK
12 days
PHA UK branded Candles of Hope are now available to order at https://t.co/dcq93SMQWr 🕯️ Join us at 8pm on #PHDayUK (Friday 7th November) as we light candles of hope in homes around the UK. Details: https://t.co/7AmModNc71
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@PHA_UK
PHA UK
13 days
We're grateful to Bisma for sharing her experiences in order to help others. Here at the PHA UK we are working on supportive resources to help those affected by this issue, and they will be available early next year.
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@PHA_UK
PHA UK
13 days
Being diagnosed with PH as a young woman brings unique challenges & many struggle with the advice not to have children. In this candid interview, PHA UK member Bisma explains how 5 years after her diagnosis she has come to accept she will not be a mother: https://t.co/RYe5ynOoYH
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@PHA_UK
PHA UK
14 days
Our October e-newsletter has landed in inboxes... so as always, don't forget to check your spam folder 📩 Anyone can sign up for these monthly email updates, which are separate from our member magazine. Subscribe here: https://t.co/Dxxkr9Cdqh
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@PHA_UK
PHA UK
15 days
💜 Will you be going #PurpleForPH on Friday 7th November? Paint your nails burgundy, don some lilac earrings, or go all out in head-to-toe violet. How about holding a non-uniform day at work or school, to raise funds as well as awareness? Details: https://t.co/KV0pgZrRrc
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@PHA_UK
PHA UK
17 days
Today is #WorldMenopauseDay so we're reminding you of our free publication to help women with PH who are navigating this time of life. Order your copy now at https://t.co/OVhqOqC0s1
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@PHA_UK
PHA UK
19 days
We're looking for people affected by #CTEPH to be part of a new study with medics & researchers to ensure patient voices help shape service development. Find out more & register your interest here: https://t.co/IQDdTvghL2
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@PHA_UK
PHA UK
20 days
Having a PH diagnosis doesn’t automatically make someone eligible to receive the COVID-19 vaccine this autumn. Find out more: https://t.co/EGF4FKehgD
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@PHA_UK
PHA UK
21 days
NEW! Add your words to our online PH Platform and make yourself heard for #PHDayUK 💬 See the platform: https://t.co/B8Uw5xtvZg 📢Leave a message: https://t.co/JzWHRvJ5wb #BreathlessNotVoiceless
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@PHA_UK
PHA UK
22 days
Couldn't make it to our event in Birmingham? You can now watch all of the expert talks and lived experience panels online: https://t.co/9VjMXyTIxu
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@PHA_UK
PHA UK
25 days
Today is #WorldMentalHealthDay so this is an important reminder that if you live with PH and need support with mental wellbeing, you're not on your own. Find out more about our support services: https://t.co/d6Iqe1wtoy
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@PHA_UK
PHA UK
26 days
📩 Could you email your MP to ask for a social media shout-out on #PHDayUK? MPs are always looking for opportunities to support constituents & many have large followings online. You'll find links to template text & more here: https://t.co/yvKvSCb3J6
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