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Are you or your child affected by the genetic defect Alpha-1 Antitrypsin Deficiency? Are you a relative of someone with Alpha-1 Antitrypsin Deficiency and have questions?

Sometimes there are moments when those affected and their relatives reach their limits, feel overwhelmed, and seek help.

Here you will find the contact details of your contact persons for Adult and Children. We are happy to provide information and are available for an exchange of experiences. We kindly ask you to respect our privacy and refrain from calling after 8 p.m. Thank you.

For questions regarding AAT deficiency in adults, please contact:

For questions regarding AAT deficiency in children/adolescents, please contact:

1. Vorsitzende Marion Wilkens

Marion Wilkens

1. Chairperson

For questions regarding AAT deficiency in adults, please contact:

Marion Wilkens, Chairwoman
Telephone service number: 0800 – 5894662 (free of charge)
E-mail: marion.wilkens@alpha1-deutschland.org

2. Vorsitzende Gabi Niethammer

Gabi Niethammer

Advisory board member

For questions regarding AAT deficiency in children/adolescents, please contact:

Ms. Gabi Niethammer, Advisory Board Member
Tel.: 040 – 78891320
E-mail: gabi.niethammer@alpha1-deutschland.org

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