American Kidney Fund @KidneyFund
National independent nonprofit fighting CKD & ESRD w/prevention, education, clinical research & financial assistance. Take #KidneyAction with @akf_advocacy! kidneyfund.org Rockville, MD Joined June 2009-
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Leigh-Ann is living with FSGS due to 2 variations of the APOL1 gene. Now that she knows the origin of her kidney disease, she’s pushing others in her family to get genetic testing. Learn more about APOL1-mediated kidney disease & join in AMKD Awareness Day:bit.ly/3IgH4sl
Everyone has two APOL1 genes. But for people with a certain variation of the APOL1 genes, there is an increased risk of developing APOL1-mediated kidney disease (AMKD). Help raise awareness by joining our efforts for AMKD Awareness Day on April 30: bit.ly/3IgH4sl
As we near the end of National Minority Health Month, AKF is proud to announce the launch a national media campaign aimed at bringing greater awareness of kidney disease within Black and Hispanic/Latino communities: bit.ly/3JvZczc #KidneyHealthForAll #NMHM24
April 30th 2024 is the first APOL1-Mediated Kidney Disease (AMKD) awareness day!Tim Hopper & I wrote this article to raise awareness of AMKD among physicians and lay people alike.@KidneyFund @nkf @nephcure @DukeKidney @itsglendar @ISGDtweets @SannaCherchiLab
April 30th 2024 is the first APOL1-Mediated Kidney Disease (AMKD) awareness day!Tim Hopper & I wrote this article to raise awareness of AMKD among physicians and lay people alike.@KidneyFund @nkf @nephcure @DukeKidney @itsglendar @ISGDtweets @SannaCherchiLab
Join AKF President & CEO LaVarne Burton and AKF VP of Patient Support & Education for a Q&A with AKF Ambassador Quenton Turner-Gee about his experience living with AMKD. Attend today's @NMQF webinar at 12PM ET: bit.ly/3UCc9xS
Ahead of AMKD Awareness Day, join AKF President & CEO LaVarne Burton and Mike Spigler, AKF Vice President of Patient Support & Education, as they sit down with AKF Ambassador Quenton Turner-Gee to discuss living with AMKD. Attend tomorrow’s @NMQF webinar: bit.ly/3UCc9xS
Mark your calendars! Join us Wed. June 5th from 6pm - 9pm at Pineapple Club, #NYC as we celebrate the expansion of the David Atkins Living Donor Assistance Fund to the New York metro area! Purchase tickets &; learn more: fundraise.kidneyfund.org/event/a-night-…
Through their advocacy on Capitol Hill and in their communities, AKF Ambassadors support people wherever they are in their fight against #kidneydisease — from prevention through post-transplant living. Learn more and join our AKF Ambassador community: bit.ly/3Jcdy7a
Turning 30 is a big milestone & many people have things they want to accomplish before the big 3-0. Donating a kidney isn’t a common item on that list. But Chris Tock added it to his list & gave his kidney to family friend Paul Violino: bit.ly/3PWHys2 #DonateLifeMonth
Autosomal dominant polycystic kidney disease (ADPKD) is a condition that causes cysts to grow in the kidneys. Because it's genetic, ADPKD is usually passed down from parent to child. Learn more on risk, symptoms, & how to talk to your provider about ADPKD: bit.ly/3ghGv6Z
🚶Get ready! AKF’s 37 Mile Challenge kicks off May 1st, but you can get started fundraising and walking NOW! #DYK – once you raise $200 you can claim your #37MC t-shirt? 👕 Get started fundraising: bit.ly/4aBLqHh
#ICYMI: All 2024 #KidneyActionWeek sessions are available online now. Catch up on our week of free virtual sessions about #kidneydisease prevention, kidney-friendly eating, #transplant & innovations in kidney disease and more! Watch: bit.ly/3U3rQwm
The most powerful way to raise awareness is by sharing personal stories, and AKF wants to hear yours. Tell us how APOL1-mediated kidney disease has impacted the lives of you or your loved ones by submitting a short video to help make others #APOL1Aware: bit.ly/3P3P9oa
Did you know that 1 in 5 Black Americans with 2 variations of the APOL1 gene have a chance of developing kidney disease? Learn more about APOL1-mediated kidney disease (AMKD) & help others become #APOL1Aware with AKF’s AMKD Awareness Day toolkit: bit.ly/3ITpD1o
#DYK: 88% of the more than 103,000 people on the national transplant waitlist need a kidney? #Livingdonor protections may help reduce wait lists. Here’s how we are working to remove the barriers potential #donors face with our 2024 Report Card: kidneyfund.org/livingdonors.
AKF is thrilled to be selected as one of the top 50 nonprofit employers in the U.S. by @NonProfitTimes and @BestCompaniesGP for the third year! Read more here: bit.ly/3Us7zSD
Getting genetic testing for APOL1 variants is crucial for understanding your risk of developing kidney diseases, especially if you're of Central or West African descent. By knowing whether you carry these variants, you can take proactive measures to monitor your kidney health and…
Become #APOL1Aware and join @KidneyFund for AMKD Awareness Day on April 30. Learn more about APOL1’s connection to kidney disease and spread the word: kidneyfund.org/APOL1aware #GeneChat
National Kidney Found.. @nkf
44K Followers 907 Following We’re fighting to eliminate preventable kidney disease, accelerate innovation, and dismantle structural inequities in kidney care. Join our fight.Jonathan Chávez @JonathanNefro
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JAMA Insights reviews the origin of APOL1 high-risk genetic variants, defines APOL1-mediated kidney disease, and discusses recommendations for screening and management. ja.ma/3WfiAYJ
I’m very honored to be working with the @KidneyFund to raise awareness of APOL1-mediated kidney disease (AMKD) and its implications for kidney health! Did you know variations in the APOL1 gene are linked to increased risk of kidney disease? Knowing whether you have the APOL1…
Being #APOL1Aware means knowing how your genes impact your kidney health. On April 30, join me, an #AKFAmbassador in recognizing AMKD Awareness Day with @KidneyFund and become #APOL1Aware. Click the link to watch MY video below: american-kidney-fund.boast.io/r/63c1c5c2-8e4…
Getting genetic testing for APOL1 variants is crucial for understanding your risk of developing kidney diseases, especially if you're of Central or West African descent. By knowing whether you carry these variants, you can take proactive measures to monitor your kidney health and…
Become #APOL1Aware and join @KidneyFund for AMKD Awareness Day on April 30. Learn more about APOL1’s connection to kidney disease and spread the word: kidneyfund.org/APOL1aware #GeneChat
To support the David Atkins Living Donor Assistance Fund, visit bit.ly/3HEeZLc
Today’s @IBEW103 & @necaboston #HeroAmongUs was diagnosed with kidney failure and needed to find a donor. Matt Glazier identified his friend, David Atkins, as a match. With a new kidney, Matt and his wife Julia have raised $50K+ to remove the financial constraints facing donors.
Made it across home plate from the pitcher’s mound. Way to go Melanie! #APOL1Aware
Play ball! AKF was thrilled to join @VertexPharma last Friday night at the Boston @RedSox game in honor of AMKD Awareness Day, which will be held April 30. Melanie Paris, senior director of strategic partnerships and education, threw out the first pitch! #APOL1Aware
Genetic conditions like APOL1-mediated kidney disease can affect you and your family. Become #APOL1aware with this information, including risk factors and symptoms. elivingtoday.com/lifestyle/heal…
Become #APOL1Aware and join @KidneyFund for AMKD Awareness Day on April 30. Learn more about APOL1’s connection to kidney disease and spread the word: kidneyfund.org/APOL1aware
@KidneyFund discussed strategies to improve healthcare access, education, prevention, and research for APOL1 in underprivileged communities during the AMKD Roundtable. Emphasis was on prioritizing marginalized populations and their involvement in the healthcare system.
I’m 1 of 13% of Black Americans with 2 APOL1 gene variants & also 77% West African. Knowing could have helped w/ my #KidneyDisease diagnosis. So I’m working with @KidneyFund to raise awareness of AMKD. Visit kidneyfund.org/APOL1aware to learn more & be #APOL1Aware #AKFAmbassador
April 30 will be the first APOL1 mediated kidney disease day for AMKD Awareness. Does AMKD impact you? Visit @KidneyFund for more information. kidneyfund.org/apol1aware
Dr. Marcelle Tuttle, a first-year fellow in the @TuftsMCKidney, is the recipient of this year's Clinical Scientist in Nephrology fellowship program from the American @KidneyFund! Congratulations Dr. Tuttle! bit.ly/4aRZKel
Become #APOL1Aware and join @KidneyFund for AMKD Awareness Day on April 30. Learn more about APOL1’s connection to kidney disease and spread the word: kidneyfund.org/APOL1aware
American @KidneyFund has awarded Tufts Medical Center researcher Dr. Marcelle Tuttle a Clinical Scientist in Nephrology Fellowship. Dr. Tuttle's research will focus on the development of pulmonary hypertension in patients with chronic kidney disease: tuftsmedicine.org/about-us/news/…
The same fearlessness and determination Alonzo Mourning exhibited during his Hall of Fame basketball career - He’s now applying towards the fight against kidney disease.
Become #APOL1Aware and join @KidneyFund for AMKD Awareness Day on April 30. Learn more about APOL1’s connection to kidney disease and spread the word: bit.ly/43RUO77 #APOL1 #APOL1Awareness #NOWINCLUDED #AMKDDay
I’m joining @KidneyFund for AMKD Awareness Day on 4/30. Those of certain African descent may be at increased risk of having APOL1 gene variants that may lead to AMKD. I encourage you to become #APOL1Aware! Visit kidneyfund.org/APOL1aware to learn more #AKFAmbassador