Sunday, July 30, 2017

Pulmonary Fibrosis Foundation Summit 2017: Nashville!

The Pulmonary Fibrosis Foundation will be holding its 4rd Summit in Nashville from November 9-11, 2017. I am planning on being there along with many other health care professionals and scientists who are passionate about raising awareness and finding a cure for PF. If you are a patient with PF or if someone you love has PF, I strongly encourage you to attend the Summit. You will have the opportunity to meet doctors, scientists, and other patients and caregivers. Many sessions are planned just for patients and caregivers. You can learn more about the Summit at http://www.pffsummit.org/

I hope to see you there!

2 comments :

  1. Doctors are not fortune tellers. This is really true. I may only imagine what hard work they have every day. Perhaps even there is no time for writing articles. As a help, I want to offer you a team bookwormlab that will help write the article. I think you may do it.

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  2. A CT scan in August of 2009 verified that I had Idiopathic Pulmonary Fibrosis. My first symptoms were cough and shortness of breath. I was on prednisone and inhalers. My blood oxygen level was 50 and i was extremely short of breath, i was barely able to breath. I went through cardio pulmonary rehab, It helped but not too long before all the severe symptoms returned. December last year, a family friend told us about Rich Herbs Foundation and their successful lungs disease treatments, we visited their website www.richherbsfoundation.com and ordered their IPF herbal treatment, i am happy to report this treatment effectively reversed my Idiopathic pulmonary fibrosis and symptoms. I am back on my feet, i walk daily now and has made me able to walk my two dogs again without shortness of breath or sudden loss of energy. My activity level is up again.

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