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Helpline open Monday to Friday, 10:00 to 18:00

People helping people with skin conditions

We are an independent, non-profit patient organisation. Since 2010 we have been bringing together people living with skin conditions, their families and the professionals who care for them.

Illustration of a diverse group of people smiling together

Our story

“We started as six people around a kitchen table, tired of feeling alone with our skin. Today we are a community of thousands.”

DermaNGO was founded by patients who wanted more than a prescription: they wanted to be understood. What began as a small monthly meeting has grown into a national network of support groups, a helpline and a respected voice for patients.

We work closely with dermatologists, nurses, psychologists and researchers, but we always remain patient-led. Our board, volunteers and members decide what we focus on, because they know best what life with a skin condition is like.


2010

founded

35

support groups

180

volunteers

What drives us

Three simple ideas guide every decision we make.

Our mission

To improve the quality of life of people with skin conditions through support, information, community and advocacy.

Our vision

A society where nobody is judged by their skin and everyone has access to the care and treatment they need.

Our values

Kindness, respect, honesty and independence. We listen without judgement and we never sell or share your data.

Milestones

2010

The first meeting

Six patients start a monthly support group.

2014

Helpline opens

Volunteers answer the first calls and emails.

2019

National network

Support groups in eight cities and online.

2024

A stronger voice

We help shape new patient-rights guidelines.

Meet the team

A small staff team and a big family of volunteers.

Portrait illustration of Anna Georgiou

Anna Georgiou

President, living with psoriasis

Portrait illustration of Dimitris Papas

Dimitris Papas

Helpline coordinator

Portrait illustration of Sofia Andreou

Sofia Andreou

Support groups & events

Portrait illustration of Dr. Helen Markou

Dr. Helen Markou

Scientific advisor, dermatologist

Independent and transparent

We are funded mainly by membership fees, individual donations and grants. Any support from companies is unrestricted, published in our annual report and never influences the information we share.

  • 48% individual donations
  • 27% membership fees
  • 17% public and foundation grants
  • 8% unrestricted corporate support

Give a few hours, change someone’s day

Volunteers run our support groups, answer the helpline and organise events. No experience needed: we provide training and a lot of kindness.