Agimuramdan1 @agimuramdan1

Pennsylvania, USA Joined November 2015

Tweets

266
Followers

251
Following

2K
Likes

6K

PKD Foundation @PKDFoundation

5 years ago

March is #NationalKidneyMonth! Over the next few weeks, we'll be sharing Voices of PKD stories, information about kidneys, and ways you can spread #PKD awareness. Check out our resources and ways to get involved 👉 pkdcure.org/kidneymonth/

0 5 12 0 0

Download Image

The DW Designs @thedwdesigns

5 years ago

March is National Kidney Month Kidney Our founder/designer Dan has a kidney disease known as PKD. ➡️ We have a tee to raise awareness for kidney disease. This month, a portion of every DW TENN teal tee will go directly to the funding for @PKDFoundation #endPKD #KidneyMonth

0 3 5 0 0

Download Image

Nicole Elizabeth Ramos #MigrarNoEsUnDelito @luzenlafrontera

5 years ago

An 8 year path to citizenship is too fucking long & likely to be taken away. Did we not learn anything from DACA? We really doing this again? People want a path to citizenship not some shitty road littered w/landmines white nationalists can detonate anytime they've got the power

4 53 303 0 5

PKD Foundation @PKDFoundation

5 years ago

To the 229 donors who helped us meet our $40,000 goal and everyone who shared our #GivingTuesday message, thank you. Thank you for supporting education, patient advocacy, and crucial PKD research. We couldn't advance our mission to give hope and our vision to #endPKD without you.

0 4 8 0 0

Download Image

PKD Foundation @PKDFoundation

5 years ago

If you or someone you care about has just been diagnosed with PKD, you probably have a lot of questions. You may be feeling overwhelmed with all of the information. We’re here to help you learn about PKD and how to manage the disease. Find out more at pkdcure.org

0 5 11 0 0

Download Video

PKD Foundation @PKDFoundation

5 years ago

Many people considering leaving a legacy to the PKD Foundation first think about including us in their will. Did you know that’s not your only option when it comes to planned giving? Check out today's blog to learn about TOD accounts. ow.ly/8xzy50C9jEE

0 3 4 0 0

PKD Foundation @PKDFoundation

5 years ago

Help find the next treatment for ADPKD when you join the nearly 2,000 patients already in the ADPKD Registry. Learn more and see how we protect your information at pkdcure.org/registry.

0 5 7 0 0

Download Video

PKD Foundation @PKDFoundation

5 years ago

Before your PKD diagnosis, you probably didn’t give much thought to phosphorus and kidney disease. But for people with PKD, consuming too much of it can be a major concern. Here's what you need to know about managing your phosphorus intake. ow.ly/dSpF50C4bjn

0 6 10 0 0

PKD Foundation @PKDFoundation

5 years ago

The University of Alabama at Birmingham, in collaboration with Children’s National Hospital in Washington, D.C., has received a five-year, $4 million grant from the NIH to create a core center for childhood cystic kidney disease. Learn more - ow.ly/qtoT50BWuXE

0 5 11 0 0

PKDF St. Louis Region @PkdStl

5 years ago

Help us find a cure for our future generation! The girls' grandma & mom have PKD. These girls each have 50% chance of inheriting autosomal dominant polycystic kidney disease (ADPKD). Visit walkforpkd.org/stlouis 2 register to walk (virtually) or donate. #WhyIWalk @PKDFoundation

0 3 8 0 0

Download Image

NPR @NPR

5 years ago

"We can no longer pretend that we don't know exactly who and what this president stands for," Michelle Obama says of Trump in a new video. "Search your hearts, and your conscience, and then vote for Joe Biden like your lives depend on it," she says. trib.al/MTb5yfc

13K 13K 36K 0 227

PKD Foundation @PKDFoundation

5 years ago

Why do you #walkforpkd? Go to walkforpkd.org/why-we-walk to download and print our template. Post your picture on social media and tag us! Don’t forget to register for the virtual Walk at walkforpkd.org

0 4 6 0 0

Download Image

PKD Foundation @PKDFoundation

5 years ago

For these siblings living 8600 miles apart, not even the pandemic could stop this kidney transplant. Read more about their journey in the @washingtonpost. #DonateLife #endPKD ow.ly/XTKs50Bqjys

0 5 9 0 0

PKD Foundation @PKDFoundation

5 years ago

We had to make a lot of changes to how we would run the Walk events this year. What's interesting is that even with all of the changes we've been through, the reasons why we walk have not. For Gary, his reasons to Walk are his wife & daughter. What's your reason to #WalkforPKD?

1 5 8 0 0

Download Image

PKD Foundation @PKDFoundation

5 years ago

The #ADPKD Registry is officially one year old! We can't wait to see what's in store with this resource making #PKD research more accessible to patients in the years to come. Read more about the Registry anniversary on the blog. #endPKD pkdcure.org/blog-adpkd-reg…

0 4 7 0 0

Malkia S. White @fromHelltoWIN

5 years ago

TODAY is PKD Awareness Day! Polycystic kidney disease (PKD) is a chronic, genetic disease causing uncontrolled growth of fluid-filled cysts in the kidneys, often leading to renal failure. Plz support @PKDFoundation! #PKDAwarenessDay #endPKD

0 9 11 0 0

Download Image

PKD Foundation @PKDFoundation

5 years ago

September 4, is #PKDAwarenessDay! Our mission this Friday is to educate others on polycystic kidney disease. Will you join us in raising awareness? pkdcure.org/what-to-know-a… #PKD #endPKD

0 17 17 0 0

PKD Foundation @PKDFoundation

5 years ago

PKD Awareness Day is THIS Friday, September 4th. ➡️ ow.ly/164z50BeY39

0 11 13 0 0

PKD Foundation @PKDFoundation

5 years ago

50% of people with #ADPKD will develop kidney failure by age 60. There's currently no cure for ADPKD. Click the link below to learn more about autosomal dominant polycystic kidney disease. pkdcure.org/what-is-adpkd/ #endPKD #PKDEDU #PKD