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Frequently Asked Questions

Quick answers to the most common questions we receive from newcomers to the association

Absolutely not. Alopecia Areata is an autoimmune disease in which the immune system mistakenly attacks hair follicles. There is no contagious component and it is not dangerous to general health.

Yes. Alopecia Areata patients are entitled to a contribution toward wig purchase within the health basket, as well as additional reimbursements through supplemental health insurance (Shaban) and private insurance policies. HeadsUp assists and guides how to exercise these rights.

JAK inhibitors are a group of modern biological medications that have shown excellent results in hair regrowth for alopecia patients. Some of these medications have been approved for use in adults and adolescents aged 12 and above. Consult a specialist dermatologist for suitability and medical approval.

HeadsUp Is Always With You

Contact us with any question, consultation or wish for support. Our volunteer team consists of experienced patients who will be happy to listen and help.
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058-5652177WhatsApp
Emailinfo@headsup.org.il

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HeadsUp Israel

The Israeli Association for Alopecia Areata (Reg. 580545994)

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Privacy Policy·Terms of Use·Accessibility Statement

The information on this site is for personal knowledge only and is not a substitute for professional medical advice, diagnosis, or treatment.

Built by Alex Ciuraru Read more

Alex Ciuraru — father of Alma, Sol & Alon, husband of Sapir. Sapir, my beloved wife, has been diagnosed with alopecia for over 10 years and copes with the many challenges the disease brings. This site was built with love for the HeadsUp Association and the community — keep your heads up, be proud of who you are, and keep being the best version of yourselves.

Be free,
live HeadsUp

"HeadsUp" is the warm and supportive home for thousands of Alopecia Areata patients — an autoimmune disease causing patchy or total hair loss. We provide medical information, emotional support and advocate for the rights of children and adults alike.

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Kids & AlopeciaContact Us

Children & Alopecia — Hand in Hand with Parents

Coping with alopecia in children requires special sensitivity, inclusion and unique tools for the social and educational environment. HeadsUp provides parents with group support, special information kits for kindergartens and schools, and community events for children so everyone feels equal and embraced.

  • Dedicated explanation kit for kindergartens and schools
  • Emotional support for parents (Zoom meetings and personal support)
  • Events, summer workshops and social gatherings for children
Happy child with alopecia
Parents Information Center

The Complete Alopecia Guide

All the professional information, available treatments and your medical rights in one place

What is Alopecia Areata?

A detailed explanation of the types of alopecia, its causes, medical diagnosis and disease progression in adults and children.

Read more →

Treatments & Medications

A comprehensive overview of existing medical treatments, including the latest breakthroughs and JAK inhibitor medications.

Read more →

Patient Rights & Reimbursements

How to receive reimbursements for wigs from the health basket, exercising rights with National Insurance, and funding assistance.

Read more →

Emotional Coping

Tools for coping with body image changes, psychological support, workshops and guided support groups for patients and families.

Read more →
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Support the Association

"HeadsUp" operates as a non-profit and all its members are volunteers. Your donations enable us to continue producing support workshops, purchasing wigs for underprivileged children, holding medical conferences and advancing patient rights in the Knesset.

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You're Not Alone: Our Supportive Community

Connect with people going through the same journey. Support, knowledge sharing and lifelong friendships

Private WhatsApp Groups

A discreet space for questions, daily mutual support and information exchange between association members.

Join on WhatsApp

Private Facebook Group

A dynamic community of over 1,500 members sharing personal stories, treatment recommendations and wig tips.

Join Request on Facebook

Online Support Meetings

Regular Zoom workshops and meetings with professionals and emotionally guided inspirational stories.