Skip Main Navigation
Page Content

Save This Event

Event Saved

MONTREAL PKD PATIENT FORUM / FORUM PATIENT MPR DE LA VILLE MONTRÉAL

PKD Foundation of Canada

Friday, 20 September 2019 from 6:00 PM to 8:30 PM (EDT)

MONTREAL PKD PATIENT FORUM / FORUM PATIENT MPR DE LA...

Ticket Information

Type End Quantity
RSVP 20 Sep 2019 Free  

Share MONTREAL PKD PATIENT FORUM / FORUM PATIENT MPR DE LA VILLE MONTRÉAL

Event Details

Venez nous rejoindre au Forum gratuit pour patients MPR à Montréal, QC! 

Join us for the upcoming FREE PKD Patient Forum in Montreal, QC!

 

La maladie polykystique des reins (MPR) est l'une des maladies génétiques potentiellement mortelles les plus courantes chez les canadiens. La MPR peut entraîner l’apparition de kystes qui font augmenter le volume de chaque reins, en détruisant leurs capacités de fonctionner.
Polycystic kidney disease (PKD) is one of the most common life-threatening, genetic diseases affecting Canadians and can result in the growth of cysts that enlarge the affected kidneys, destroying its ability to function.

 

Les patients et leurs proches sont invités à se joindre à ce forum pour:
Patients and their loved ones are invited to join this forum to:

 

• Apprendre ce que le diagnostic de la MPR signifie pour vous ou un de vos proche, lors de la présentation du Dr. Guillaume Bollée, néphrologue et directeur de la clinique de maladies rénales rares au Centre de recherche sur les maladies rares et génétiques chez l’adulte de l’Institut de recherches cliniques de Montréal (IRCM);

Learn about what a PKD diagnosis can mean for you or a loved one, as well as how PKD can be managed from Dr. Guillaume Bollée, Nephrologist and Director of the Kidney Rare Disease Clinic at the Research Centre on Rare and Genetic Diseases in Adults of the Montreal Clinical Research Institute 
(IRCM);


• Obtenir des renseignements sur les ressources et les systèmes de soutien mis à votre disposition par la fondation de la MPR. Présentation de Jeff Robertson, directeur exécutif de la foundation;
Hear about what resources and support systems are available to you and your loved ones from Jeff Robertson, Executive Director, PKD Foundation of Canada;

 

• Période de questions et réponses avec Dr. Guillaume Bollée, et Jeff Robertson; et
Have your questions answered during a Q&A period led by Dr. Guillaume Bollée and Jeff Robertson; and,

 

• Rencontrer d’autres personnes vivant avec la MPR dans votre communauté.
Meet other people living with PKD in your community.

 

Goûter léger vous sera offert. / Light snack will be offered.

 

Admission gratuite. Stationnement de ville. Metro Sherbrooke. Tous sont bienvenus!
Free admission. City parking. Metro Sherbrooke. All are welcome!

 

L’inscription 18h00, début de la presentation à 18h30 pile.

Please note, registration is at 6:00 p.m. and the presentation will start at 6:30 p.m. sharp.

  

 

About the Speaker:

Dr. Guillaume Bollée, Nephrologist, Director of the Kidney Rare Disease Clinic at the Research Centre on Rare and Genetic Diseases in Adults of the Montreal Clinical Research Institute (IRCM).  

Dr. Guillaume Bollée is a nephrologist and Director of the Kidney Rare Disease Clinic at the Research Centre on Rare and Genetic Diseases in Adults of the Montreal Clinical Research Institute (IRCM). Dr. Bollée also practices medicine at the Centre hospitalier de l’Université de Montréal (CHUM) and is an Assistant Clinical Professor in the Department of Medicine at the Faculty of Medicine of the Université de Montréal. He is the author and co-authored of numerous articles including rare and genetic renal diseases issues.

Have questions about MONTREAL PKD PATIENT FORUM / FORUM PATIENT MPR DE LA VILLE MONTRÉAL? Contact PKD Foundation of Canada

Save This Event

Event Saved

When & Where


Institut de recherches cliniques de Montréal (IRCM), Jacques-Genest Auditorium
110 Avenue des Pins
Montréal, QC H2W 1R7
Canada

Friday, 20 September 2019 from 6:00 PM to 8:30 PM (EDT)


  Add to my calendar

Organizer

PKD Foundation of Canada

The PKD Foundation of Canada is the only national organization that promotes programs of research, advocacy, education, support and awareness in order to discover treatments and a cure for polycystic kidney disease, and improve the lives of all it affects.

  Contact the Organizer

Interested in hosting your own event?

Join millions of people on Eventbrite.

Please log in or sign up

In order to purchase these tickets in installments, you'll need an Eventbrite account. Log in or sign up for a free account to continue.