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| The LPHS Foundation is here to
help you. Becoming a member will put you in a better position for
support, help and advice from our advisors and other members. It
doesn't cost anything to join and you will come to understand the illness
and realise that you are not alone with this rare problem.
We provide up-to-date information on how to cope and what to do. Our information is contributed by other members and medical experts. Our Foundation is based between this site and our Yahoo! Club, which is the LPHS Assosiation - You can go to the club just now and look around but you won't be able to use any of the features, such as chat until you are a registered member. To Register with us all you have to do it e-mail me at the address below. Just Supply the following Information: Your Name (Required)
I will review your e-mail as soon as possible and invite you to the club once you e-mail has been approved. You don't have to be officially
diagnosed with LPHS to join - because LPHS is quite a hard illness to properly
diagnose. As long as you are experiencing the symptoms - pain in
the kidney area, hematuria (blood in the urine) and possible contractions
of the kidney.
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| Registration: [email protected]
Enquiries: [email protected] |
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rights Reserved
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