PHA Canada welcomes a new volunteer “Knowledge Philanthropist”, Lisa Harder, in its pulmonary hypertension patient support team

Lisa Harder is PHA Canada’s newest Knowledge Philanthropist. These are specialized volunteers help the organization fulfill its mission. Each Knowledge Philanthropist serves the pulmonary hypertension community in their own way. Depending on their professional background, they develop resources, content from current research projects, help raise awareness, and more! Lisa brings a unique perspective as both […]

PHA Canada welcomes a new volunteer “Knowledge Philanthropist”, Lisa Harder, in its pulmonary hypertension patient support team Read Post »

The UK Pulmonary Association’s “Listening Line” support service provides dedicated time to talk through worries or concerns about emotional or mental wellbeing

The “Listening Line” is a free, confidential supportive call service is available to all members of the UK Pulmonary Hypertension Association, PHA UK, their family and friends. It is operated by experienced PHA UK staff, who are retired from the National Health Service (NHS). They are skilled and patient listeners, with many years of experience

The UK Pulmonary Association’s “Listening Line” support service provides dedicated time to talk through worries or concerns about emotional or mental wellbeing Read Post »

The Pulmonary Hypertension Association, PHA, launches a new “Peer Mentor Program”

The Pulmonary Hypertension Association, PHA, has recently launched a new “Peer Mentor Program”, to replace the Email “PHriends” program. This initiative connects patients and caregivers with a mentor who can help them navigate their pulmonary hypertension journey. Read more and find a mentor at this link on the PHA website

The Pulmonary Hypertension Association, PHA, launches a new “Peer Mentor Program” Read Post »

The UK’s Pulmonary Hypertension Association, PHA UK, offers an e-support service to patients, family members and caregivers

As not everyone is comfortable talking on the phone the PHA UK has set up an e-support online service to assist with emotional wellbeing, practical queries and problem-solving, signposting and connections. Contact the PHA UK at support@phauk.org

The UK’s Pulmonary Hypertension Association, PHA UK, offers an e-support service to patients, family members and caregivers Read Post »

The UK’s Pulmonary Hypertension Association (PHA UK)’s “Listening Line support service” offers dedicated time with a pulmonary hypertension professional to talk about mental wellbeing

The PHA Uk’s Listening Line support service offers its members and families dedicated time with a pulmonary hypertension professional to talk through concerns about mental wellbeing. Weekly appointments last for 45 minutes and are available in blocks of six. Read more and book an appointment at this link on the PHA UK website

The UK’s Pulmonary Hypertension Association (PHA UK)’s “Listening Line support service” offers dedicated time with a pulmonary hypertension professional to talk about mental wellbeing Read Post »

PHA Canada’s “PH Buddy program”, was developed during the COVID-19 pandemic to help patients stay safe and socially connected in uncertain times

“Staying connected to others in your community — even while practicing social/physical distancing — is an important part of staying well”. This is the rationale behind PHA Canada‘s “PH Buddy program”. Find out more about the program and sign up to become a “PH Buddy” by visiting PHA Canada’s dedicated website page at this link

PHA Canada’s “PH Buddy program”, was developed during the COVID-19 pandemic to help patients stay safe and socially connected in uncertain times Read Post »

The Pulmonary Arterial Hypertension (PAH) “Companion Program”, an initiative to support patients developed by Janssen

Janssen’s Pulmonary Arterial Hypertension (PAH) Companion Program connects patients to a trained PAH Companion who provides one-on-one educational support to help with prescribed Janssen PAH medication. The company specifies that the program is intended to supplement understanding of the prescribed therapy, and does not provide medical advice or replace a treatment plan from the patient’s doctor, nurse,

The Pulmonary Arterial Hypertension (PAH) “Companion Program”, an initiative to support patients developed by Janssen Read Post »

The Pulmonary Hypertension Association (PHA)’s “Email PHriends” initiative offers patients, caregivers and parents support with a caring and knowledgeable member of the community

The Pulmonary Hypertension Association (PHA)’s “Email PHriends” are volunteer patients and caregivers who are available to answer questions and chat through email with other members of the pulmonary hypertension community over a period of three months. The PHA specifies that the “Email PHriends” cannot offer medical advice but can share what they’ve learned along the

The Pulmonary Hypertension Association (PHA)’s “Email PHriends” initiative offers patients, caregivers and parents support with a caring and knowledgeable member of the community Read Post »

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