Support Group in the DFW area

Of course, we'll give you lots of support in this group. I know it's not the same as LIVE. However, it has really helped me feel like I'm not such an oddball, hypochondriac whiner. Your pain is real and all of us on this site know exactly how you feel. Please feel free to ask any questions, vent, offter your successes, whatever you feel like...we're all in this together.

Peace,

Connie

Respectfully,

Denise

Well, that's a good question...I never considered that. Honestly, I just jumped right in.. You can look at past threads and see that just about anything is up for discussion as Lyme and coinfections can manifest themselves everywhere in the body.

You could start by telling us your 'story.' Are you seeing an LLMD? What have you done for treatment? How long have you known you have Lyme? Do you have lingering symptoms?

I think there are some common sense guidelines posted somewhere...like no swearing (the occasional slip happens, but we try ). the main thing is to be respectful of each other...no personal attacks. Oh and no listing of our doctors on the posts. We need to protect our doctors' privacy and choice to treat us.

So, come on in, the 'water' is just fine

Peace,

Connie