Phimosis Foundation International

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The Phimosis Foundation International is an educational charity. Its mission is "[t]o provide clear, stigma-free information, compassionate support, and accessible resources to individuals affected by phimosis, empowering them to make informed choices about their health and well-being."[1]

The website of Phimosis Foundation International appears to have been created in September 2025.

Phimosis Foundation International is advised by a three-member Independent Clinical Advisory Board.[2] All members of the Advisory Board are from nations that do not advocate non-therapeutic circumcision. No member of the Board is from the United States.

Phimosis Foundation International urges conservative, foreskin-conserving treatment for most cases of phimosis. Circumcision is advised only for:

  • When you have suffered long-term or severe phimosis.
  • Recurrent infections.
  • Foreskin scarring (e.g., from Lichen Sclerosus).
  • When all other treatments have failed or aren’t possible.[3]

See also

References

  1. REFweb Anonymous (August 2025). Mission statement., PFI. Retrieved 27 August 2026.
  2. REFweb Anonymous (September 2025). Leadership Team, PFI. Retrieved 26 August 2026.
  3. REFweb Anonymous (September 2025). Treatment Options, PFI. Retrieved 27 August 2026.