Searching for Pkd Support Community information? Find all needed info by using official links provided below.
https://www.pkdinfo.com/support-resources
Whether you’re sharing your story, listening to someone else’s, or catching up on the latest scientific breakthroughs in the understanding of PKD, being part of a community can be inspiring and healing. Get connected today, and explore some resources and patient-focused organizations within the PKD community. This is not an exhaustive list.
http://forums.pkdconnection.org/
May 18, 2019 · Index page. PKD Connection Voices of PKD. Welcome to the PKD Foundation's Discussion Forums ... Talk to other parents who are caring for children with PKD. 19 Topics 66 Posts Last post by ... Supporting Someone with PKD Supporting Someone with PKD Talk to family, friends, caregivers and others who know and support someone with PKD. 11 Topics 32 ...
https://connect.pkdcure.org/
With PKD Connect, no one will ever face polycystic kidney disease alone. Because patients, family and loved ones will always be connected to others who understand firsthand what you’re going through. Whether you are looking for information, resources or just a shoulder to lean on, PKD Connect gives you the support to keep hope within reach.
https://connect.pkdcure.org/online-community/
PKD Connect Online Community is an online support group that is dedicated to offering a friendly, safe and supportive place for individuals and their families to share their stories and experiences with PKD. As a member, you can connect with other people impacted by PKD and contribute to ongoing conversations.
https://connect.pkdcure.org/just-diagnosed/
The PKD Foundation is here to help you learn about PKD and how to manage the disease while maintaining a high quality of life. We are here to help you get connected with others in the PKD community who can help support you and ensure that you do not face PKD alone.
http://www.forums.pkdconnection.org/viewforum.php?f=3
May 18, 2019 · View forum - Living with PKD. PKD Connection Voices of PKD. Welcome to the PKD Foundation's Discussion Forums . ... user-submitted content, comments and opinions, and they do not necessarily reflect the views and opinions of the PKD Foundation. Information shared in the forums is not medical advice. ... Looking for support
https://www.dailystrength.org/group/polycystic-kidney-disease-pkd
Polycystic Kidney Disease (PKD) Support Group. Polycystic kidney disease (PKD) is a progressive, genetic disorder of the kidneys. It occurs in humans and other organisms. PKD is characterised by the presence of multiple cysts (polycystic) in both kidneys. The disease can also damage the liver, pancreas and rarely the heart and brain.
The PKD Foundation is the only organization in the U.S. solely dedicated to using PKD Research to find PKD treatments for polycystic kidney disease. ... Community and Support. You’re not alone. Find a mentor, call our Hope line, or join a Chapter.
https://www.facebook.com/PKDsupportpage/
Hi! I just started this page for PKD Support. I am a current dialysis patient with PKD on 3 waiting lists. I have lost 5 members of my family to PKD, including my own Father. I would like to start a place where people with PKD can come, share their stories, their events, and PKD related organizations.Followers: 652
http://support.ecommunity.com/
SUPPORT PORTAL English (US) Representatives
How to find Pkd Support Community information?
Follow the instuctions below:
- Choose an official link provided above.
- Click on it.
- Find company email address & contact them via email
- Find company phone & make a call.
- Find company address & visit their office.
