Calendar

Feb
3
Wed
WEBINAR | Free Your Mind: Set Your Life Story Free Through Conversation
Feb 3 @ 7:00 pm – 8:30 pm
WEBINAR |  Free Your Mind: Set Your Life Story Free Through Conversation

Free of charge | Open to everyone

In this first webinar of Free Your Mind, Jeanne Gravfort will talk about the approach and how you can use it as a way to better understand yourself and those around you. Later on, you will have the opportunity to register for a course to learn more about the approach (more information below).

WHEN?
Wednesday, 3rd of February 
19:00 Central European Time
18:00 in Portugal, England
20:00 in Finland, Greece

REGISTER HERE!

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What is Free Your Mind?
Free your mind is an approach where you share your thoughts, feelings and experiences with people who live with the same life conditions as you. By talking and listening to others you get the possibility of being free – being able to understand your life story in a new and different way. It is an opportunity to join a community by telling your own story. A place where you can be a complete person in spite of your difference from others.

Having a Rare Disease
As a person affected by a rare disease you may experience life giving you many challenges that can seem overwhelming. You may live your life feeling sad that you are not able to do the things you want to do. You might be frustrated about the fact that you cannot live out your expectations for yourself and your life. You might feel lonely and everyday life might seem hopeless.

What is it about?
In Free your mind you will share your thoughts, feelings and experiences with people who live with the same life conditions as you. By talking and listening to others you will get the possibility of being free – being able to understand your life story in a new and different way.

Our starting point is an existential theme that every participant talks about taking turns. You will talk from your own life experiences without interruptions or questions from the other participants. Free your mind offers a safe space of confidentiality. A space where there are no taboo topics, no requirements or expectations.

Who’s Jeanne?
Jeanne Gravfort is a pastor with a lot of experience in the rare disease field. Through her studies and work, Jeanne has worked with theories of identity and memory in times of mourning and crisis and through trauma research. Furthermore, she has a specified education in mourning of the soul. Finally, Jeanne has counseled parents of handicapped children and she is a theological consultant at the Rare Disease Helpline in Denmark.

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COURSE:

The European Huntington Association offers a course in the spring of 2021 – maybe it’s something for you? It is free of charge, but you have to be a member of a local Huntington’s disease association. If you are interested in joining the course after the first webinar – here are some practical information:

  • One group consists of 4-5 participants
  • We will meet a total of six times every other week
  • The aim of the course is that you will be able to run your own support groups using the Free your mind method.

 

Feb
23
Tue
Improving care for rare disease patients in Europe (Rare Disease Day Webinar)
Feb 23 @ 3:00 pm – 4:00 pm
Improving care for rare disease patients in Europe (Rare Disease Day Webinar)

Free of charge | Open to everyone

In this webinar, we will be discussing care of rare disease patients in Europe, focusing on rare neurological diseases, and providing different perspectives: from the clinician to the patient’s perspective and from a European level to a more local one with examples from France, Germany and Hungary.

The webinar will start with short presentations by the speakers followed by a discussion.

SPEAKERS:

  • Holm Graessner, coordinator of the European Reference Network for Rare Neurological Diseases (ERN-RND)
  • Donna Walsh, executive director of the European Federation of Neurological Associations (EFNA)
  • Sophie Bernichtein, project manager of BRAIN-TEAM in France
  • Tobias Mentzel, patient advocate at ELA Germany
  • Maria Judit Molnar, Professor of Neurology and director of Semmelweis University’s Institute of Genomic Medicine and Rare Disorders, Hungary

WHEN?
Tuesday, 23 of February 
15:00 Central European Time
14:00 in Portugal, England
16:00 in Finland, Greece

SIGN UP HERE.

May
5
Wed
WEBINAR | Oral Care & Huntington’s: Keeping the mouth healthy
May 5 @ 7:00 pm – 8:30 pm
WEBINAR | Oral Care & Huntington’s: Keeping the mouth healthy

Free of charge | Open to everyone | Online

Together with Annette Carlsson, we’re running a webinar on how to maintain a healthy mouth and strong teeth in people with Huntington’s disease.

During the webinar Annette will talk more about how to manage oral health and demonstrate several tools that will make oral care easier in daily life. It is free of charge and open to everyone (both professionals and family members/carers).

Background:

One of the corner stones for Quality of Life is good oral health. For people with Huntington’s there are many problems that affects the oral health. Dry mouth as well as blisters and sores can cause pain and difficulties in eating, speaking and to perform oral care.  Toothache and lack of teeth affects even the mental status. Swallowing difficulties increase the risk of aspiration. It is of extra importance to maintain a good oral health and thereby minimize the risk of injurious bacteria reaching the lungs. 

Speaker: Annette Carlsson

Annette is a Dental hygienist at the Mun-H-Center and Hospital dentistry in Göteborg, Sweden. She’s also the chairperson of the Swedish Huntington Association.

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WHEN: 5. May, 19:00-20:30 Central European Time
PLATFORM: Zoom 
Registration will follow soon