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Sites submitted to this category should provide information about camp programs for individuals with Cystic Fibrosis.

Programs encompassing more than one disability or illness (e.g. lung disease, learning disabilities, etc.) should be suggested to Recreation: Camps: Special Needs.

English-only sites. Information in other languages should be suggested to the appropriate category in World/.

Camps for people of all ages with Cystic Fibrosis.

These include day, respite, and residential (overnight) programs. Many camps also provide programs for family members of those living with an illness or disability. Some camps offer year-round activities; some have only summer and/or holiday programs.

Universities, hospitals and clinics that specialize in Cystic Fibrosis care.
Annual and semi-annual conferences and meetings to discuss Cystic Fibrosis.
Sites where the main purpose is to promote a fund-raising event.
News releases on recent developments and treatments.
This category contains sites for organizations, associations, and societies which provide support and information or are involved in Cystic Fibrosis research projects.

Sites for foundations which provide funding for CF causes should be suggested to the /Fundraising subcategory.

English-only sites. Information in other languages should be suggested to the appropriate category in World/.

Groups that provide information on Cystic Fibrosis (CF) or work together on research.
Site where the major intent is to memorialize someone who had Cystic Fibrosis.
There is currently no description created for this category.

All sites or pages submitted to this category may be more technical in nature, but must contain information of use to patients, their families, and caregivers.

Websites designed for the education and training of medical professionals and providers should be submitted to the appropriate category in Health/Medicine/.

English-only sites. Information in other languages should be suggested to the appropriate category in

Sites listed here will represent support networks with a physical address and/or a web presence. Those with a physical address may also be submitted to the relevant Regional/. subcategory.

English language sites only. Please submit other language sites to the appropriate category in World.

Sites in this category serve the support needs of people with Cystic Fibrosis, their families and caregivers.

These groups, communities, or meeting places provide an opportunity for people with a common experience (such as a condition or disease, or a care-giving role) to share their concerns, and to seek and offer information and advice.

Read each site's PRIVACY POLICY carefully, before providing personal information.

These sites are for educational and support purposes only. Please consult your doctor or other health care provider before making any lifestyle changes that may adversely affect your condition.

For sites that primarily discuss sweat testing, nasal potential difference and any new method that may be developed. Not for blood tests, CVS, or amnio which would more appropriately go under the linked category of Genetic_Testing.
Information related to testing (diagnostic, gentic and others) for Cystic Fibrosis.
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Last update: Sunday, June 1, 2014 10:24:11 AM EDT - edit