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Link to original content: http://web.archive.org/web/20070129011028/http://www.vhl.org/healthcare/index.html
Caring for Your Health
The Wayback Machine - http://web.archive.org/web/20070205023921/http://www.vhl.org:80/healthcare/index.html
Basic Facts About VHL
Managing Your Health
Information for Health Care Professionals
Research
About the VHL Family Alliance
Press Room
Families, Friends, Physicians, & Researchers working together
to improve diagnosis, treatment, & quality of life for people affected by von Hippel-Lindau disease.

 

Membership

Services

Local Support Groups

Online discussion

Handbook

DNA Testing

Search

VHL Links

Feedback

Contact Us

 

Until 1993, little was known about defenses against VHL. Through concentrated sharing of their experiences and their expertise, family members and health care professionals and researchers are making progress, and we are learning better defenses.

Information

is the key to success in managing a rare condition like VHL. You cannot expect every health professional to know about VHL. You need to be involved in your own health care, keep track of your appointments, follow up when necessary, and take an active role in managing your health.

Your Key Contributions to research -- not just money!

  • VHL Tissue Bank keeps surgically removed tumor tissue on file so that researchers will have the cells they need to study.
  • VHL Research Database collects information from affected people so that we can provide some statistical information to researchers, making it easier for them to obtain data and therefore encouraging them to do more research on VHL.
  • And of course, helping to support research, through fund-raising as well as your own donations. Every little bit helps! It is only through research that we will find better ways to keep tumors from forming, or at least keep them small, and reduce the need for surgical intervention.

Services

Other family members at risk

  • DNA testing for VHL is available now to most families and can be a useful tool in determining who is (and is not) at risk.
  • We can supply Brochures to share with relatives and friends. Samples are available with your membership packet, and more can always be obtained from VHLFA

Local support groups

Since we are a relatively small population, thinly spread all over the world, we are mostly a communications network -- telephone, fax, E-mail, ham radio -- whatever works! There are groups formed or forming in all regions of the United States, as well as in Canada, and other countries.

VHL Symposium (every two years) and conferences(annually)

Membership

Your donations are what makes our services possible. Please send what you can to

VHL Family Alliance
2001 Beacon St, Suite 208
Boston, MA 02135-7787 USA

We're delighted that you found this page, and look forward to meeting you and working with you. Our goal is to make the world better for ourselves and our children, and, no matter what comes, to make sure we all have a Very Happy Life!

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