New diagnosis of Lyme - support groups?

[Guest guest]

After a very long year of many doctors and mostly a diagnosis of fibro. we have

arrived here! My high school senior is now essentially being home schooled due

to her pain and other symptoms affecting her ability to make it school. We are

seeing a Lyme specialist and are starting by going after the co infections

first. I am so sad to see how hard the treatment is on her. She is so much worse

since she started all the meds. & supplements! I try to hold onto the feeling of

this being progress, at least we have a real diagnosis, but it is emotionally

exhausting seeing her suffer both physically and emotionally.

I am enquiring as to the pros and cons of local support groups. I have heard

mixed reviews, support and peer interaction is the goal but is that what she

will get? I have heard they can be emotionally tough as you get caught up in

everybody elses struggles and symptoms. Also i would lovw to find her peer

support as in with other teens. We live in N. CA. Any input is appreciated,

thanks.