phaware global association was founded by a group of pulmonary hypertension awareness activists. Comprised of patients, caregivers, and medical professionals, phaware is dedicated to engaging the global community to forge a new course to a cure.
http://www.phaware.global/
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phaware.global | phaware.global Reviews
https://phaware.global
phaware global association was founded by a group of pulmonary hypertension awareness activists. Comprised of patients, caregivers, and medical professionals, phaware is dedicated to engaging the global community to forge a new course to a cure.
phaware.global
PARTNERS — phaware.global
http://www.phaware.global/partners
PH BY THE NUMBERS. ON AIR WITH PHAWARE. Rose Colored Mask Blog. In Life With PH Blog. Stanford Race Against PH. Rare Disease Day 2016. PH BY THE NUMBERS. ON AIR WITH PHAWARE. Rose Colored Mask Blog. In Life With PH Blog. Stanford Race Against PH. Rare Disease Day 2016. Our partners are instrumental in helping us make PH history. Their generous support and collaboration allows phaware. Learn more www1.actelion.com. And at www.cteph.com. Mdash; Mattie Stepanek, poet. Become a #phaware Partner. The informat...
phaware ESPN podcast — phaware.global
http://www.phaware.global/phaware-espn-podcast
PH BY THE NUMBERS. ON AIR WITH PHAWARE. Rose Colored Mask Blog. In Life With PH Blog. Stanford Race Against PH. Rare Disease Day 2016. PH BY THE NUMBERS. ON AIR WITH PHAWARE. Rose Colored Mask Blog. In Life With PH Blog. Stanford Race Against PH. Rare Disease Day 2016. ON AIR WITH PHAWARE. Rose Colored Mask Blog. In Life With PH Blog. The experience - espn los angeles. The Discussion: PH Awareness Month 2016. Engage For A Cure 2015. On Twitter @laferncusack @ESPNLosAngeles. Engage for a cure. B. The info...
MISSION — phaware.global
http://www.phaware.global/mission
PH BY THE NUMBERS. ON AIR WITH PHAWARE. Rose Colored Mask Blog. In Life With PH Blog. Stanford Race Against PH. Rare Disease Day 2016. PH BY THE NUMBERS. ON AIR WITH PHAWARE. Rose Colored Mask Blog. In Life With PH Blog. Stanford Race Against PH. Rare Disease Day 2016. Was founded by a group of pulmonary hypertension awareness activists. Comprised of patients, caregivers, and medical professionals, phaware. Is dedicated to engaging the global community. Working on the forefront of technology, phaware.
phaware press releases — phaware.global
http://www.phaware.global/phaware-press-releases
PH BY THE NUMBERS. ON AIR WITH PHAWARE. Rose Colored Mask Blog. In Life With PH Blog. Stanford Race Against PH. Rare Disease Day 2016. PH BY THE NUMBERS. ON AIR WITH PHAWARE. Rose Colored Mask Blog. In Life With PH Blog. Stanford Race Against PH. Rare Disease Day 2016. ON AIR WITH PHAWARE. Rose Colored Mask Blog. In Life With PH Blog. Press REleases and news articles. H Awareness Night: Breathless On Broadway. Pulmonary Hypertension News 7/4/16. Phaware: How a Global Network for PH Awareness Got Started.
phaware365™ app — phaware.global
http://www.phaware.global/phaware365
PH BY THE NUMBERS. ON AIR WITH PHAWARE. Rose Colored Mask Blog. In Life With PH Blog. Stanford Race Against PH. Rare Disease Day 2016. PH BY THE NUMBERS. ON AIR WITH PHAWARE. Rose Colored Mask Blog. In Life With PH Blog. Stanford Race Against PH. Rare Disease Day 2016. Global disease. Global awareness. Help make pulmonary hypertension history! It's a snap with the phaware365 app. Show the world you are #phaware of this rare, life-threatening lung disease. Customize with PH facts. STEP UP WITH A SELFIE:.
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livingono2forlife | Living On O2 for Life
https://livingono2forlife.wordpress.com/author/livingono2forlife
Living On O2 for Life. Being dependent on oxygen doesn't mean your life is over. A Story in a Story. October Means Flu Shots. Living On Oxygen for Life. I hope if you haven’t yet gotten your flu shot and are not the few who have an allergic reaction to its ingredients, please get the flu shot. It can really help if you get a cold. It will help prevent that cold from turning into the flu or even pneumonia. Posted in Doctor Appointments. It took 25 years. but I did it! Living On Oxygen for Life. We just ne...
CTEPH.com | Additional Resources
http://hcp.cteph.com/resources
This site is intended for US Healthcare Professionals. Contact Bayer Medical Information. The following resources may offer additional information about CTEPH to help you and your patients. American Association for Respiratory Care (AARC). American Association for Thoracic Surgery (AATS). American College of Cardiology (ACC). American College of Chest Physicians (ACCP). American College of Rheumatology (ACR). American Heart Association (AHA). American Thoracic Society (ATS). Or call 1 800 FDA.
CTEPH.com | CTEPH Resources
http://www.cteph.com/resources
This site is intended for a US audience. SYMPTOMS AND RISK FACTORS. DIET AND EXERCISE TIPS. DISCUSSING WORK and PERSONAL LIFE WITH YOUR DOCTOR. CAREGIVERS NEED HELP, TOO. This Site is for a US audience. The following downloadable materials and websites can provide you with additional helpful information about chronic thromboembolic pulmonary hypertension (CTEPH) and pulmonary hypertension (PH). Of course, always talk to your doctor first if you have questions or need information. Or call 1 800 FDA 1088.
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phaware.global
PH BY THE NUMBERS. Rose Colored Mask Blog. In Life With PH Blog. Stanford Race Against PH. Rare Disease Day 2016. PH BY THE NUMBERS. Rose Colored Mask Blog. In Life With PH Blog. Stanford Race Against PH. Rare Disease Day 2016. Engage for a cure. Welcome to phaware.global. Pulmonary hypertension (PH) is a rare, life-threatening lung disease that can lead to right heart failure. To quickly connect and discover. HOW TO SUPPORT OUR INNOVATIVE PH RESEARCH. How you can participate #phaware activations. Ask yo...
www.phaware.org
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Column 1 - DIV. REGISTER TO RECEIVE UPDATES FROM US OR TO MAKE A DONATION. Make sure Password and Confirm Password are same and not empty. Password and Confirm Password cannot be empty. Select the most applicable answer. A family member has PH. I am interested in PH research. I am just discovering PH. I am not at my PH treatment goal. I would like to take part in a PH case study. Click on the podcast player to Listen and Share episodes with your friends. I'M AWARE THAT I'M RARE:. To tell us about yourself.
"BLOGGING FOR PULMONARY HYPERTENSION AWARENESS"
BLOGGING FOR PULMONARY HYPERTENSION AWARENESS". Monday, November 22, 2010. Shaye's Story (written by her mother, Teresa). Here is our story of PH and how it all began. Was our reaction. They said she needed to be taken to the Texas Childrens hospitals ER. I left work and went by to get the xrays to take with me. Picked up Shaye, while my husband stayed home with the other 3 children. We left for the hospital which was about a 30 minute drive from Katy where we live. Links to this post. Tammie S's PH Story.
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