CWL06_Interview Liz Morgan PatientsLikeMe

CWL06_Interview Liz Morgan PatientsLikeMe

Named one of Fast Company's 2017 Top 10 Most Innovative Companies in Biotech, PatientsLikeMe is on a mission to put patients first! Learn more about PatientsLikeMe from Liz Morgan, Director, Member Experiences. She answers questions on how the company is committed to helping patients live better. Then log onto PatientsLikeMe.com to join a network of over 500,000 people to share experiences, provide support, and track symptoms.Lupus is a life altering and challenging disease to live with. Lupus is a chronic, autoimmune disease that can damage any part of the body to include, but is not limited to skin, joints and/or life organs. According to the Lupus Foundation of America, Inc.* about 1.5 million people, worldwide, have a form of Lupus.-----Host Note: From the heart of experience, I am well aware of the related difficulties that come with living with Lupus. I was diagnosed with Lupus at the age of 16. At this time, Lupus was still a very curious disease. I was told that I would not live more than ten years after being diagnosed. Yet, life trials and errors prove that I am not dead yet! I am currently in the process of writing a memoir about combating Lupus. More research has enabled many Lupus patients to live fulfilling lives. ========================================­===Learning to live successfully with lupus.========================================­===**Click Below to SUBSCRIBE for More Videos:www.youtube.com/user/LupusLiar========================================­===**Click Below to Sign up for the FREE living with lupus tips via email:goo.gl/li06i0**FOLLOW, LIKE, TWEET, SHARE**Twitter: www.Twitter.com/TheLupusLiarFacebook: www.facebook.com/TheLupusLiarInstagram: www.Instagram/thelupusliarPinterest: www.Pinterest.com/thelupusliarWebsite: www.TheLupusLiar.com

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Jaksot(11)

CWL09_My Lupus and My Hair

CWL09_My Lupus and My Hair

CWL09_My Lupus and My Hair I was asked about whether or not my hair came out while being diagnosed with lupus and how long my hair has been growing while locked. I'll be happy to answer your questio...

24 Helmi 20227min

TLL Moment_002 Get Through It

TLL Moment_002 Get Through It

Get through it. It’s not about getting past it, it’s about getting through it.

13 Touko 20192min

TLL Moment_001 Admitting Defeat

TLL Moment_001 Admitting Defeat

Every now and then you have a moment. Here’s thoughts from a moment of admitting defeat. It happens!

19 Maalis 20192min

CWL08_PeerApproachestoLupusSelfManagement

CWL08_PeerApproachestoLupusSelfManagement

Want to be contacted? Go to http://bit.ly/palsstudy to complete the interest form! The Peer Approaches to Lupus Self-Management (PALS) Study Could Be Right For You! This is a research study that con...

19 Tammi 201944min

CWL07_A Lupus Holiday

CWL07_A Lupus Holiday

Give yourself a ‘Lupus Holiday!’ A short rant on reminding yourself to be present for your health this holiday season. Consider changing your mindset this season to self-care, smart decision making, a...

23 Joulu 20188min

CWL05_A Conversation with Tanisha Davis| Lupus Nephritis Patient and Advocate

CWL05_A Conversation with Tanisha Davis| Lupus Nephritis Patient and Advocate

Conversations with Lupus: An Interview with Lupus Patient Tanisha Davis-SmallsHow does a mother of three, diagnosed with lupus nephritis live a full life while living with lupus? Watch this interview ...

3 Helmi 201729min

CWL04_ Annetta Talks About Her Battle with Lupus

CWL04_ Annetta Talks About Her Battle with Lupus

Annetta's shares a little of her story. Annetta was diagnosed with Systemic Lupus on January 4, 2000. This day changed her life. As the old by Annetta, "I knew it was going to take a toll on me. It wa...

15 Joulu 201629min

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