Hello, anyone out there? anyone reading this?

[Seasprite]

Or can you recommend some other lyme disease sites?

Especially support groups?

I have been dx with Lyme and am still skeptical for myself about morgs.

Though I do have much in common with what is reported here.

[jonsi]

Hi seasprite,

I tested positive for lymes and take liquid balsamea extract daily. Lazar light therapy (which stimulates mitochondria growth in the cells, ie more oxygen in the system) can give you more energy.

I hope you can find a support group near you.

Itwl,
~jonsi

[ladycolorado]

Hi Seasprite I hear you. Hi. You would like a local support group? I might know something.

This is a link for Lyme Disease support Groups in the United States:
The Lyme Disease Network Support Groups Listing .

This is a directory of Lyme Disease support groups for countries:
The Lyme Disease Network Support Groups Listing ,

May I also suggest joining a yahoo local Lyme group.

I hope this helps.

(LC)

[Dove]

I just viewed some pictures (ask.com) of lyme disease and I have a stronger opinion now that it is the same thing as Morgellons. I think that the skin is red because of the build up of fluid at the site.

They have a link to a support group, I do not know any more about it than that.

I was trying to do a comparison of emerging diseases that relate to the skin, nerves and mind which I had started about a year ago and was not able to complete. Also, has anyone else heard about the bugs that came back on the space shuttle or from space?

Did I miss a thread on this.