Contact with peers and exchange of experiences can help and provide relief. After all, it turns out you are not the only one with these symptoms.
To connect with fellow members, you can use the following facilities as a member:
- On Facebook, the association has set up a private group: Sharing group Tietze and Costochondritis patients association
- Every spring we organize a day somewhere in the country where our general meeting is combined with a fun activity.
- Every autumn a weekend takes place somewhere in the country where there is room for exchange between fellow members, fun, activities and information. Our stay is always at a beautiful location where we can also enjoy delicious culinary delights.
- Every year there is a New Members’ Day to get acquainted with the association and each other, including partners.
Contact: deelgenoten@tietze.nl
It’s coming again … the “new member day”!
Again in 2025, we’re organizing a meeting for new members of our association.
And this Saturday, Oct. 11, at a central location in the country.
A ‘new member day’ …. why?
We want new members to quickly ‘feel at home’ within our association and know what we have to offer. In doing so, it is nice for everyone to know where they can find the right information.
We also like to offer the opportunity to share experiences and thus give recognition and acknowledgement to their experiences.
In addition, it will be a fun interactive workshop, with a delicious lunch and socializing.
Some members like to bring their partner; he or she can then also hear what is going on. Coming along is allowed, but not a must. A membership would of course be nice, but it is not necessary for this activity. For ‘non-members’ we ask a contribution of € 15 p.p.
As soon as more is known and members of our association can sign up, we will mention this on the website. And there will be a timely mailing with details and the registration form.
So keep an eye on your mailbox and our website and mark both dates in your calendar!
Meanwhile, if you have any questions, feel free to ask at deelgenoten@tietze.nl
Board Association of Tietze and Costochondritis Patients.
