The APF Supports & Helps those needing assistance! Call the APF 1.866.APF.3635 or message us on FB support groups. #patientscomefirst #patienteducation #support #raredisease #APF

Are immunizations/vaccinations safe for people with acute porphyria? We therefore recommend that patients with acute porphyria receive necessary vaccinations, in accordance with established guidelines, under physician recommendation.

CLICK ON THE LINK: canva.com/design/DAFMOLj…

UPDATE: An email went out today with 2023 Reenrollment directions, including options to apply for Reenrollment by text, email, online, QR code, or paper application. Your 2023 Reenrollment dates are dependent on whether you are in the Purple or Teal Reenrollment Groups.

Call the APF first with any questions you may have. Important to get accurate information. 1.866.APF.3635 Just world wide Opportunity to share your experience with AHP.

If you need a patient or physician packet emailed to you for free please message us. Were happy to assist you

Medical Moment- Ferritin: a protein present in the liver, which binds and stores iron. A small amount of ferritin (serum ferritin) circulates freely in the blood, where it may be measured. To learn more click porphyriafoundation.org

Please take a moment on Giving Tuesday to give to the APF. You are the ones that keep us moving in education & research for the Porphyrias. facebook.com/donate/8166259…

Holiday Announcement-gofundme.com/f/hope-for-the…

Please friends, give someone in the Porphyria community a donation today. fb.watch/hfpBa080nB/?mi…

If you need assistance with Porphyria please contact the APF today. Receive a free patient & Dr. Packet by email. Reply to [email protected]

EPP & XLP PATIENT MEETING Free to attend!

Exciting News! The APF store is now open fun new shirts, necklaces, and more goodies get your today either order by phone or by custom ink link. Go to porphyriafoundation.org Next Click on APF Store

Today is Rare Disease Day across the globe!! DARE TO SHOW YOUR RARE! We put Patients First and have dedicated ourselves to Rare Disease and Porphyria for over 40 years!💜 We are not so rare together and we are here for you everyday! #apf #rarediseaseday #porphyria #purplepain

With Canadian Association for Porphyria announcing EPP Patient Day Virtual Event! Presentation by Porphyria Expert Dr. Karl Saardi of GW MFA w/ Q&A, children & adults share & a MAJOR announcement for EPP Patients - Don't miss this event! Comment below or contact [email protected].

Today at 1pm ET - Spotlight on Acute Porphyrias featuring Porphyria Expert Dr. Roy E. Smith w/ Q&A. AHP patients will also present. Please email [email protected] to register #PAW2023 #SpotlightPorphyria #porphyria #PorphyriaAwarenessWeek #porphyriawarriors

Last day so please click! We have partnered with @RecordatiRareUS to raise awareness of #Porphyria. CLICK THIS LINK ➡️ bit.ly/3L2izl5, and Recordati Rare Diseases will donate $5 (up to $5K) for every click. Let’s Fight Porphyria Together! #SpotlightPorphyria #PAW2023

La APF con Asociación Porfiria , SMP, Eileen Hudson, PhD , Fundacion porfiria , Costa Rica Porfiria y Argentina Centro de Porfiria les invitan a un Zoom con el experto Ronny Kershenovich🎗 🇮🇱🇲🇽🧬🩺🎗 con preguntas y respuestas. Para registrarse, contacte a [email protected] #porfiriajuntos

Calling all book lovers! You're invited to join a new APF book club starting August 8th. Connect monthly with other members & forget about porphyria for a while. Email [email protected] to join. #Porphyria #MoreThanPorphyria #PorphyriaStrong #BookClub #ReadBooks

NEW SHIRTS AVAILABLE!! V-necks, long & short sleeves & tons of colors! Visit: PorphyriaFoundation.org/apf-store/ Creative design by APF member Andrew McManamon Andrew McManamon #porphyria #americanporphyriafoundation #porphyriaitsinmyblood #apfstore #porphyriaapparel #porphyriafoundation