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menu menu education and support pkd connect center pkd blog pkd events walk for pkd fundraise your way pkd connect conference engage spread the word become a volunteer become an advocate chapters join a local chapter volunteer with us international affiliates research research & funding clinical trials tolvaptan about the foundation executive leadership board of trustees scientific advisory committee who we are media careers financial information sign up pkd emails blog social facebook twitter youtube instagram pinterest linkedin home what is pkd? what is pkd? polycystic kidney disease (pkd) is a chronic, genetic disease causing uncontrolled growth of cysts in the kidney, often leading to kidney failure. it affects all racial and ethnic groups equally. adpkd what are the symptoms? what are cysts? how is adpkd diagnosed? what are the stages of adpkd? what are the related health complications? kidney 101 arpkd what are the symptoms? how is arpkd diagnosed? what causes arpkd? what are the related health complications of arpkd? what is pkd? adpkd what are the symptoms? what are cysts? how is adpkd diagnosed? what are the stages of adpkd? what are the related health complications? kidney 101 arpkd what are the symptoms? how is arpkd diagnosed? what causes arpkd? what are the related health complications? living with pkd is there a cure for pkd? while no cure currently exists for pkd, there is one pharmaceutical treatment approved in the u.s. for patients with adpkd. living with pkd just diagnosed exercise nutrition pregnancy and pkd chronic pain management finding a clinic working with your doctor research clinical studies donating your kidneys for research pkd treatments in pipeline dialysis & transplant pre-transplant preparation types of kidney donation life after transplant about living donation kidney allocation system (kas) dialysis news & information pkd blog keep updated resource library living with pkd living with pkd just diagnosed exercise nutrition pregnancy and pkd chronic pain management finding a clinic working with your doctor research clinical studies donating your kidneys for research pkd treatments in pipeline dialysis and transplant dialysis pre-transplant preparation types of kidney donation life after transplant about living donation kidney allocation system (kas) news and information pkd blog keep updated resource library get involved fundraising events, advocacy and volunteering whether it is walking annually at one of our 50 local walk for pkd events, advocating on a local or national level, or participating in chapter activities to fundraise for pkd research, there are many ways to get involved in the cause! community voices of pkd peer mentor program online community about chapters events walk for pkd fundraise your way 2018 conference engage spread the word become a volunteer become an advocate get involved pkd connect center community voices of pkd peer mentor program online community about chapters events walk for pkd fundraise your way pkd connect conference engage spread the word become a volunteer become an advocate about the foundation executive leadership board of trustees scientific advisory committee who we are media careers financial information donate general donation monthly donation tribute donation planned giving walk for pkd donation social facebook twitter youtube instagram pinterest linkedin subscribe find posts about: research advocacy education awareness new handbook provides help and education for arpkd parents and patients category arpkd education date posted august 17, 2018 author pkd foundation we’re excited to feature our new arpkd patient handbook as a resource for both parents of children with arpkd and older arpkd patients who are interested in learning specific information about their disease. we recently reached out to michele karl, […] read more comments local volunteer leader gives an inside look at pkd foundation chapters category chapters date posted august 15, 2018 author pkd foundation my name is erin burden and i live in metro atlanta with my husband, christopher, and our three children. we first learned of pkd when my oldest daughter’s ultrasound revealed some kidney abnormalities in utero. since she is a fraternal […] read more comments “the call” and kaley, part ii category voices of pkd date posted august 10, 2018 author pkd foundation after being placed on the waitlist, receiving the call for a kidney transplant is a happy occasion for many pkd patients. the chance that pkd, with its genetic nature, might not end with a transplant can lead a family down […] read more comments pkd connect resource center offers peer mentoring services category education pkd connect date posted august 3, 2018 author pkd foundation if you, a family member or friend are impacted by pkd, sometimes you need advice, encouragement or a shoulder to lean on from someone who knows firsthand what you’re going through. enter our pkd connect peer mentor program. this new […] read more comments fundraising tips for the fall walk for pkd season category walk for pkd date posted july 31, 2018 author pkd foundation our annual walk for pkd is just around the corner! as our signature fundraising event, 100% of the funds you raise go to pkd research to help find treatments and a cure. our community fundraising strategist, julie russell, shares her […] read more comments pkdf staff member nicole harr shares her reflection pre-transplant category positivity transplantation date posted july 27, 2018 author pkd foundation our own nicole harr, director of community engagement, has spent the last two years sharing pieces of her journey as she’s prepared to receive a kidney transplant. now, as the day of her surgery approaches, she shares her reflections on […] read more comments we’re all human category pkd will not beat me date posted july 26, 2018 author pkd foundation sometimes the littlest thing at an unexpected time can trigger emotions that have been building up for a while. for me, it was a hospital food tray. on dec. 2, 2017, i woke up severely ill with a high fever. […] read more comments and how was your day? part 1 category voices of pkd date posted july 23, 2018 author pkd foundation as many pkd patients know, pkd can often be accompanied by other ailments. join guest blogger rob herman as he shares his and his family’s story about how pkd has impacted their lives: though it has yet to be officially […] read more comments check out highlights from our new pkd connect resource center category education date posted july 20, 2018 author pkd foundation my name is zseraldina ferenczi and i am the community outreach coordinator at the pkd foundation. i am excited to tell you about an important new resource for anyone impacted by polycystic kidney disease (pkd). it’s a web portal called […] read more comments 2018 pkd connect conference: favorite moments category convention date posted july 16, 2018 author pkd foundation whether you were at the 2018 pkd connect conference or if we missed you this year, you’ll want to catch up on what attendees had to say about the event! check out the video below, and hopefully we’ll see you […] read more comments subscribe enter your email address to subscribe to this blog and receive notifications of new posts by email leave this blank: leave this blank too: do not change this: your email: share share this facebook twitter pinterest search for resources search categories view by category pkd will not beat me 234 pkd health notes 141 recipes 82 positivity 81 q and a 71 research 43 determination 41 awareness 34 walk for pkd 31 education 29 transplantation 24 voices of pkd 24 knowledge 20 staying healthy 18 pkd foundation news 15 staff update 13 arpkd 12 advocacy 11 adpkd 7 run for pkd 6 family life 4 board of trustees 3 convention 3 chapters 3 diy for pkd 2 pkd connect 1 categories subscribe enter your email address to subscribe to this blog and receive notifications of new post

URL analysis for pkdconnection.org

https://pkdcure.org/blog/category/board-of-trustees/
https://pkdcure.org/living-with-pkd/dialysis/
https://pkdcure.org/get-involved/spread-the-word/
https://pkdcure.org/blog/check-highlights-new-pkd-connect-resource-center/?showcomments=1#comments
https://pkdcure.org/make-a-donation/?amountfill=50
https://pkdcure.org/what-is-pkd/adpkd/kidney-101/
https://pkdcure.org/blog/category/advocacy/
https://pkdcure.org/blog/day-part-1/?showcomments=1#comments
https://pkdcure.org/blog/category/recipes/
https://pkdcure.org/blog/were-all-human/
https://pkdcure.org/blog/2018-pkd-connect-conference-favorite-moments/
https://pkdcure.org/blog/were-all-human/?showcomments=1#comments
https://pkdcure.org/get-involved/advocacy/become-an-advocate/
https://pkdcure.org/what-is-pkd/arpkd/how-is-arpkd-diagnosed/
https://pkdcure.org/blog/pkd-connect-resource-center-offers-peer-mentoring-services/

Whois Information

Whois is a protocol that is access to registering information. You can reach when the website was registered, when it will be expire, what is contact details of the site with the following informations. In a nutshell, it includes these informations;

WHOIS LIMIT EXCEEDED - SEE WWW.PIR.ORG/WHOIS FOR DETAILS

  REFERRER http://www.pir.org/

  REGISTRAR Public Interest Registry

SERVERS

  SERVER org.whois-servers.net

  ARGS pkdconnection.org

  PORT 43

  TYPE domain

  REGISTERED unknown

DOMAIN

  NAME pkdconnection.org

NSERVER

  NS1.DREAMHOST.COM 64.90.62.230

  NS3.DREAMHOST.COM 66.33.205.230

  NS2.DREAMHOST.COM 208.97.182.10

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