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What we do with your contribution or donation

  • Seeking and maintaining contacts with Medical proffessionals and patient organisations.
  • Connect with research programs  for treatment protocols and diagnose tools.
  • We provide you with an information package.
  • We published the book “leer er maar mee leven” about coping with Tietze and/or costochondritis.
  • We published a DVD with interviews with patients, a GP and a physio therapist.
  • We organise national and regional member contact days.
  • You receive periodic newsletters.
  • We maintain and update  the website with the latest developments.
  • We search for latest news and information on Tietze and costochondritis.
  • To keep the membership fees as low as possible, we predominantly use e-mail to correspondent with our members. If you however have objections or if you don’t have access to internet and email, we can correspond by surface mail.
  • We stand up for your rights and interests.

All the activity’s are don by voluntary workers

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