October 11, 2008 7:20am
Dear Journal
Gorgeous day here again.... midday and still not dressed... not enough energy to care today. Flared up , bloated and …
October 10, 2008 6:57am
Beautiful , sunny morning here ... fresh autumn day.. love this time of year - the sort of day where I feel motivated to do loads of …
October 9, 2008 3:40pm
Today not dissimilar from yesterday as far as pain goes... lately I feel like Eeyore, kinda blue and I have a definate flattened mood, …
Hi again. How are you? Are you feeling any better? Here's a hug for you! :) Cheryl
Hi! I was thinking about you this morning. How are you doing? I hope well, but let me know! :) Cheryl
Hi! I have RA and Lupus also. I was diagnosed with RA at 28 and SLE at 39. I can tell the difference between the two. When the RA is acting up I am more stiff and achy and when Lupus is flaring I am more tired and pain is more severe in my joints and muscles. I am on 6mg of Prednisone, Celebrex, Enbrel inj., and Kadian for pain. I also get IV's of vitamins and minerals weekly which has really helped both diseases! I LOVE Eeyore too! I think he just looks like how I feel.LOL Welcome. I am in the Lupus group. If you ever want to talk I am here. :) Cheryl
Hi Sharon39, welcome to the MCTD group, and to this site. I also have UCTD and sound a lot like you, from what you said in your journal, lol. Would you like to be friends? Sounds like we have things in common, I feel like Eeyore a lot too, especially the last few days, lol! I hope you are having a nice evening. Big Hugs, Sheri
Diagnosed 3+yrs with UCTD, mixture of lupus and RA - looking for ways to manage inflammation better, and avoid flare ups
Diagnosed 5+years ago and looking for new or different ways to manage pain.
Diagnosed about 3 years ago, and hoping to learn more about disease management etc
Diagnosed 3+yrs ago with Lupus and RA and currently looking for more ways to support myself and reduce inflammation/disease activity
