Welcome to PHA Australia
PLEASE CHECK YOUR EMAIL ADDRESS DETAILS - Some emails have bounced. Have you changed your email address and forgotten to tell us? We can't communicate with you if it's not current and we would hate it if you miss out on our activities.
TIME TO CHECK IT NOW
Details on how can be found if you go to the message board and click on the Pulmonary Hypertension forum. Details are in the relevant message at the top of the box. (NOTE: members if you have forgotten your password required to access the message board please contact us and we will help you)
For more details contact Joan Godber at joan@phaaustralia.com.au
IT'S BACK ! - PUCKER UP 4 PH 2010
www.puckerup4ph.com
A JOINT AWARENESS CAMPAIGN ORGANISED BY PHA UK AND SUPPORTED BY PHA AUSTRALIA AND PH ASSOCIATIONS AROUND THE WORLD
This campaign is designed to raise awareness of PH and at the same time create awareness that there are support groups in your area that can help. This campaign is a fantastic way to spread the word and raise awareness, and maybe some funds for PHAA, and will run from May to November 2010. You can put your photo in the gallery to show your support for PH sufferers around the world.
Every lip print counts and your single print could be the one that secures the Guinness World Record. Help us make as many people as possible aware of this rare disease that , left untreated, has devistating effect. Posters, entry forms and lother documents can be downloaded from www.puckerup4ph.com by clicking the Get Involved tab at the top. Choose the region and when you click on Australia the Australian information will come up ready for you to down load.
For instructions and more details contact Joan at joan@phaaustralia.com.au
PHA Australia brings hope and a better understanding of pulmonary hypertension to many families throughout the Australia and the world, we invite 2009 into our lives with advances in PH treatment and more answers.
A fabulous gift at this time would be a donation to our site, so we can continue to work at raising awareness of this disease. You can do this by clicking on the donation button below. PHA Australia is a registered non profit organisation.
Pulmonary Hypertension may be known as:
Pulmonary Hypertension (PH), Pulmonary Arterial Hypertension (PAH) and Idiopathic Pulmonary Arterial Hypertension (IPAH).
Mission Statement
The mission of Pulmonary Hypertension Australia is to provide hope, support and education, and to promote awareness and to advocate for the pulmonary hypertension community.
PHA Australia is registered non profit organisation, managed by a committee that is elected every Annual General Meeting. This committee is made up of PAH patients, family members and friends.
Our main focus for this website is to provide support, create awareness and provide the latest information and research on Pulmonary Arterial Hypertension. We do this by offering members a message board for PAH information as well as message boards for friendly conversation and fun. The application process although easy to navigate, must meet the approval of our moderators. This restriction keeps our site private and safe for our members. We have three levels of membership- registered members, financial members and clinical members. Please see the criteria for each of these under the “Join/Donate” tab.
Together we are stronger
A FINAL NOTE : MAKE SURE YOU HAVE : http://www.phaaustralia.com.au/ with the "au" if you do not have the "au" on the end of the url address you will be directed to our basic site without the message boards - we had to secure both domain names.
Thanks Annie
PHA Australia would like to thank PHA USA for their ongoing support:
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PHA Australia is proudly sponsored by
