I finally did it!

:banana: I began my first website. A whole new adventure for me. The word of my new website was let out on Wednesday. We were not ready to have it officially “launched” just yet. :yikes:

You may subscribe (register) to Lyme-Aware, it’s free. I hope you do. You may use a fake name, just as long as you list a valid email address. (You may also learn a lot.) Feel free to subscribe to the Newsletter too.

Lyme-Aware’s, [url=http://lyme-aware.org" onclick="window.open(this.href);return false;]http://lyme-aware.org[/url], site is, nowhere near completion. However, some of the content is available for you to view. There is still plenty of content to be added and re-arrangements to be made—quite an undertaking but I am ready for the challenge. This site includes U.S.A., Canadian, and other countries sites.

congrats lydian82

Great site. Everyone should go take a look.
I have a friend with Lyme Disease.
She is very courageous.

Good luck to you! It looks like an interesting site. I almost didn't click on it though because I wasn't really sure what it was about. You might want to give an intro into it. With so many bad sites and viruses around a lot of people won't click on links to other things they know nothing about.

:Thanks: Becky and Chocolove.

Becky, Does your friend live in the area? I was asked by someone if I would start a support group here in Conifer. I wasn't so sure about it because I really don't know many people here. May be I should reconsider the idea? Hmmmm.

Chocolove,

Do you mean I should add something more on my site? Or, on here.

The first two sentences of my Mission statement are right next to my Logo. I guess uncertain what you mean.

On the About Us tab, I removed what I had there; it was suggested that I be more personal "reveal myself more". Why am I doing this? So, I am torn if I should put a head picture of me and share more of my experiences with Lyme disease and Babesia. Would you want to hear about how I got so ill, I lost my job and had to be bathed and clothed and lost my night vision for several months and later with Babesia, lost my hearing for a few months?
Really :sadKeenex: I didn't want it to be so lame. It's not about me, but to prevent what happened to me from happening to others.

Any feedback please.

I meant on here. On your post about your site.

Hopefully those with Lyme Disease are trying colloidal silver along with other treatments. Silver is used to control viruses and bacterias.