WELCOME!

About 70,000 adults and children in the UK may have Polycystic Kidney Disease or PKD - life-threatening inherited conditions that can cause renal (kidney) failure and affect other organs in the body.

We support those affected, their families and carers. We raise awareness and fund research.

Find out more about PKD.

SUPPORT LINE

0300 111 1234

ADPKD Information & Support Day

Category
Information & Support Days
Date
Saturday, 1st February 2020 10:00 - 16:00
Venue
Fetal Medicine Research Institute, London, SE5 8BB
Email
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Hosted by renal consultants, Dr Catriona Shaw and Dr Ellie Asgari

Download the programme | Download the venue map and directions

Learn about ADPKD (Autosomal Dominant PKD) and the latest research

  • Put your questions to the medical experts
  • Share your experiences with others

Free to attend and everyone welcome - patients, families, carers and medical professionals

Talks on:

  • The basics of ADPKD
  • Genetics
  • ADPKD and children
  • Diet and lifestyle
  • Research
  • Kidney transplant
  • Psychological impact of chronic kidney disease

Lunch and refreshments included.

There is no charge, but a donation is welcome to help cover the costs.

 
 

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PKD Charity is a Member of

  • Fundraising Regulator Website
  • Visit PKD International website
  • Visit Ciliopathy Alliance website
  • Visit the Genetic Alliance UK website
  • Rare Disease UK Website
  • Specialised Healthcare Alliance Website
  • FEDERG Website
  • Visit EURORDIS website