← Return to How do you cope with Mixed Connective Tissue Disease (MCTD)?

Discussion

How do you cope with Mixed Connective Tissue Disease (MCTD)?

Autoimmune Diseases | Last Active: 2 days ago | Replies (107)
Comment receiving replies
@believe1

Looking to chat comparatively on mctd

Jump to this post

Replies to "Looking to chat comparatively on mctd"
kleffew | @kleffew | Dec 7 6:59am

Good morning, I am coming up on my 8 year anniversary of being diagnosed with MC. T. D , good and bad days, you just have to take it day-by-day.

VIEW AND REPLY
Colleen Young, Connect Director | @colleenyoung | Dec 7 10:56am

@believe1 and @kleffew, I moved your posts to this discussion:

- How do you cope with Mixed Connective Tissue Disease? https://connect.mayoclinic.org/discussion/mctd-265a2b/

I did this to help connect you with other members living with mixed connective tissue disease (MCTD) like @callieb1102 @gdcm @mctd43years @dee5 @cindia1 @erikab @marye2 @bouregard3 @margar1 and many others.

See all MTCD discussions: https://connect.mayoclinic.org/group/autoimmune-diseases/?search=MCTD#discussion-listview

@believe1, is this a new diagnosis for you? What helps you manage the emotional side of living with MCTD?

VIEW AND REPLY
Becky, Volunteer Mentor | @becsbuddy | Dec 7 9:59pm

@believe1 Welcome to Mayo Clinic Connect! You’ve come to the right place to discuss your disease. And I see that you’ve already gotten in discussions with other members. Feel free to ask any questions that might come up!

VIEW AND REPLY