Welcome to the
community
With the help of our communities in cities across the country and beyond, we provide a forum for patients who want to join in the fight to find treatments and cure for PKD.
Connect with us to find out how you can make a difference in the lives of thousands in the U.S. and millions worldwide.
2024 Phoenix
Walk for PKD
Sunday, October 20
Chaparral Park
Registration/site opens: 8 a.m.
Join us this fall and be a part of the largest gathering of the PKD community.
Sign up today and bring treatments to patients faster with 100% of each donation funding life-saving research at
walkforpkd.org/phoenix.
If you have questions, email us at phoenixwalk@pkdcure.org.
Phoenix Community Meeting
Navigating PKD Life:
How PKD continues to impact our health, and the lives of those we love-and-lost.
Join us for our upcoming community meeting!
Gil Izraeli, LMSW and Heidi Buller, RN from Mayo Clinic will join us to discuss managing emotional challenges while living with PKD.
Whether you’ve been recently diagnosed, been fighting the battle for years, or living well post-transplant, this open discussion will be focused on life with PKD. You can choose to share your story or just listen to others talk about what they wish they had known earlier—and how that information is helping them today. We’ll also be discussing how this disease has impacted our families, while honoring those we’ve loved and lost. Mayo Clinic AZ wants you to know that they stand ready to support your PKD journey. Attend this meeting so our collective voice can be heard.
Event Details:
Wed., Sept. 18, 2024
11:30 am – 1 pm
Mayo Clinic Hospital
1st floor, conference room 227
5777 E. Mayo Blvd.
Phoenix, AZ 85054
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Registration for the 2024 Walk for PKD is now open! Find your walk at walkforpkd.org. |
The PKD Foundation is excited to the announce the newest cohort of Centers of Excellence, Partner Clinics, and Pediatric Clinics. If you are looking for the right healthcare providers to help you manage living with PKD, visit our Centers of Excellence page to learn more about the program and to find a Center of Excellence, Partner Clinic, or Pediatric Clinic.
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There’s a new way ADPKD Registry participants can step up to provide hope today, and for future generations. The nation’s first dedicated ADPKD Registry is now also one of the first patient registries of any kind to integrate patient-provided health records. Share your health records through your provider’s online portal with a few simple steps on the ADPKD Registry.
Now, as always, the PKD Foundation is committed to our mission of giving hope, advocating for patients, and building a community for all impacted by PKD. We'll continue supporting our community by providing important resources and timely updates on social media. If you have questions or need help navigating this unprecedented health crisis, we are here for you. Email or call (844) PKD-HOPE.
Masara Azooz
PKD Connect Ambassador
Masara is a junior undergraduate student at Arizona State University pursuing a bachelor of science in Pharmacology/Toxicology. She initially started out on the pre-pharmacy track, but came into the realization after 2 years of retail pharmacy experience at CVS that she would feel the most fulfilled and compelled if she was the first healthcare professional to hear a patient’s story-so that in return-she would be able to devise a patient centered plan reducing many discrepancies she encountered in her earlier career.
Now, she holds a position as an emergency room scribe in which she feels much ecstatic to experience medicine at its core. Her strive to better patient’s lives doesn’t stop here but is continued through her ongoing research project that tests a drug for its ability to increase reproductive longevity.
Her path to joining the PKD foundation was inspired by past encounters with troubled PKD patients that were in a clouded mental state. As an aspiring physician and perhaps a nephrologist, these short-lived snapshots quickly transitioned her into the climax of her future endeavors- function as a fruitful resource and mentor for kidney patients and her prospective patients. She and her parents, including two sisters, live in Arizona and love to enjoy the outdoors as much as possible
Risa Simon
PKD Connect Ambassador
Risa Simon is a fierce patient advocate who is dedicated to empowering PKD patients at every turn. Whether she’s speaking, writing, mentoring or volunteering for the PKD Foundation, the National Kidney Foundation or the American Association of Kidney Patients, her inspirational message touches the hearts of both professional and patient audiences.
Of course, it wasn’t until she was diagnosed with the same disease that took her father in his early 40s, and put her brother on dialysis in his late 30’s, that she decided to join the PKD community as a life-long student. What she learned dramatically changed her trajectory.
Now celebrating nearly 13 years as a preemptive transplant recipient (from a living, unrelated kidney donor), she spends the majority of her time giving back by helping fellow kidney patients seek their best life possible. The life she now lives.
You may know Risa as a conference speaker, transplant industry consultant, PKD peer mentor, advocate, author and video producer—or, as the creator of the new mobile app “DONOR SEEKER.” For those who don’t know Risa, she looks forward to learning more about your PKD journey at a future Phoenix Chapter meeting or PKDConnect conference.
Amanda Culver
Walk for PKD Ambassador
I am the new Walk for PKD Ambassador. Ask me about the Phoenix Walk for PKD!
Page last updated July 2023