Your impact

Where your donation goes

Daily therapy cannot be skipped. Every contribution helps a family continue treatment without interruption.

Enzymes with every meal

Without pancreatic enzymes, food cannot be digested. Children with CF take them with every meal, every day.

Inhalations & physiotherapy

Clearing thick mucus from the lungs is done 1–4 times a day, for life.

Antibiotics & vitamins

Lung infections need prompt treatment, and fat-soluble vitamins are essential.

Awareness & education

Campaigns, educational materials and activities that make CF known to families, doctors and society.

Other ways

How you can help

1

Volunteer

Help organise campaigns, charity runs and charity matches.

Write to us
2

Become a partner

Companies and institutions can support our long-term programmes.

Get in touch
3

Spread the word

Share our educational resources — awareness saves lives and speeds up diagnosis.

Resources

Frequently asked questions

Where does the money go?

Donations are used for medicines, therapy, inhalation and physiotherapy equipment, and for cystic fibrosis awareness activities in Kosovo.

Can I donate from abroad?

Yes. Use the association’s IBAN and SWIFT code for an international transfer, or contact us for other options.

Can I donate medicines or equipment?

Yes — please contact us first so we can make sure the medicines or equipment match patients’ current needs.

How can I become a member?

Our members are parents of children with cystic fibrosis. Write to us through the contact page and we will guide you.