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Potter's Syndrome Webring

Welcome to the Potter's Syndrome Webring.

This ring was created for parents who have lost their babies to Potter's Syndrome. Potter's Syndrome is very rare and so there is little information out there about it. Most people don't hear about it until someone they love or they themselves are faced with the diagnosis. This ring will hopefully link together those who have any experience or information at all. If you know of ANY reliable information about Potter's Syndrome, please email me. The more people know, the more research will be demanded. Please join this ring if you have a page with information about Potter's or if you have lost a child or have created a page for a friend or family member who has lost a child to Potter's. Also, below is a link to a support group for Potter's Syndrome parents. Please keep the URL in mind just in case someone says to you, "I never even knew what Potter's Syndrome was..." There is support for them and they do not have to be alone.

Potter's Syndrome Support Group

Fill out the form below and a ring code will be emailed to you with your id in it. This way all you have to do is copy and paste it to your page. Once the code is there, email me and I will check for it and add you to the ring.

Submit site to the Potter's Syndrome Webring
Site Title:
Site URL:

Please choose a password. (Don't forget it!!)
Keywords: Enter up to 20 keywords to describe your site.
Description: Enter a short description of your site.

Take this image and upload it to your page.

Once you have entered the HTML code into your page and uploaded your graphic, your page should look like this:

[Potter's Syndrome Webring] Member of
The Potter's Syndrome
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Email Gara
and let me
know that you are
ready to join
the Potter's Syndrome Webring!

Email Rene' If You Have Questions!