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... Step 1 — Navigate to “Account Settings.”Step 2 — Find the username section and tap “Change.”Step 3 — Enter your new username, then tap the “Change Username” button to save your changes. ...
Getting Started on MyLupusTeam
... Step 1 — Navigate to “Account Settings.”Step 2 — Find the username section and tap “Change.”Step 3 — Enter your new username, then tap the “Change Username” button to save your changes. ...
... THANK YOU for being a MyLupusTeam member! ...
New and Improved Changes to MyLupusTeam
... THANK YOU for being a MyLupusTeam member! ...
... What do you find helps you the most? ...
Symptoms That Affect MyLupusTeam Members the Most
... What do you find helps you the most? ...
... On MyLupusTeam, more than 214,000 members come together to ask questions, give advice, and share their stories with others who understand life with lupus.Which skin symptoms affect you the most? What do you do to protect your skin and stay comfortable? ...
Skin Symptoms That Affect MyLupusTeam Members the Most
... On MyLupusTeam, more than 214,000 members come together to ask questions, give advice, and share their stories with others who understand life with lupus.Which skin symptoms affect you the most? What do you do to protect your skin and stay comfortable? ...
... Members of MyLupusTeam responded to our survey to share how they are affected, and what matters most to them in lupus. What lupus symptom has had the biggest effect on your life? Share with other members in a comment below. ...
Lupus and Race: What Matters to MyLupusTeam Members
... Members of MyLupusTeam responded to our survey to share how they are affected, and what matters most to them in lupus. What lupus symptom has had the biggest effect on your life? Share with other members in a comment below. ...
... Add someone to your team when: You see a post that you like in the Activity Feed You get an email notification that someone in your area just joined and their story resonates with you You find someone in the Meet Others section who shares your diagnosis, symptoms or treatment Are you feeling shy or nervous about adding someone to your team? ...
Get the most out of MyLupusTeam by tailoring your own team!
... Add someone to your team when: You see a post that you like in the Activity Feed You get an email notification that someone in your area just joined and their story resonates with you You find someone in the Meet Others section who shares your diagnosis, symptoms or treatment Are you feeling shy or nervous about adding someone to your team? ...
... As always, we’re sharing the findings of our research with the MyLupusTeam community. You can see highlights of the survey results in the slides below. Have you tried online doctor visits? How was your telehealth experience? Leave a comment below or start a conversation on MyLupusTeam. ...
The Results Are In: How MyLupusTeam Members Think About Online Doctors’ Visits
... As always, we’re sharing the findings of our research with the MyLupusTeam community. You can see highlights of the survey results in the slides below. Have you tried online doctor visits? How was your telehealth experience? Leave a comment below or start a conversation on MyLupusTeam. ...
... Share your experience in the comments below, or start a conversation by posting on MyLupusTeam. ...
More Than Half of MyLupusTeam Members Surveyed Are Not Satisfied With Their Doctors
... Share your experience in the comments below, or start a conversation by posting on MyLupusTeam. ...
... On MyLupusTeam, more than 233,000 members come together to ask questions, give advice, and share their stories with others who understand life with lupus.How does lupus impact your general health or emotional health? What advice do you have for others living with this chronic disease? ...
Can Lupus Impact Quality of Life? Insights From Those Who Have It
... On MyLupusTeam, more than 233,000 members come together to ask questions, give advice, and share their stories with others who understand life with lupus.How does lupus impact your general health or emotional health? What advice do you have for others living with this chronic disease? ...