VitLife

Our Support Services

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Our friendly team of volunteers all have experience of how vitiligo can affect your life. Whilst our services should never replace the advice of medical professionals, we are here to listen and signpost you to accurate information about the condition.

Vitiligo Society UK Facebook Forums

We believe in the power of creating a safe, supportive community. Our facebook forums exist to provide a safe space for people living with vitiligo to share stories, information, experience and ask any questions you might have. Our team of volunteers work hard to moderate these forums so that you are kept safe from miss-information and abuse.

Click HERE to join our Facebook group

Click HERE to join our Parent Support Facebook group

Please note that in order to be accepted into a group you need to provide all the request information in your application to join.

The VitLife – Our Online Community Magazine

The VitLife is our online Member’s magazine. Our members donate to the Society each year and enable us to exist and support people living with vitiligo. Our magazine is the way we thank our members for their generosity. We publish articles every month aimed at educating, creating awareness and helping people to live well with vitiligo. Non-members can access 2 free articles a month, and are welcome to JOIN our Society as members to help support our work. Members can log in, save their favourite articles, and comment or ask questions about articles.

Follow this link to visit The VitLife: www.vitiligosociety.org/VitLife

Vitiligo Support Drop-In Service

Every month we hold a short drop in session for people who want to see and chat to our volunteers.

All our volunteers are living with vitiligo and have gone through their own personal journey with the condition. Whilst many now celebrate their skin, they each recall a time when they struggled with confidence, self worth and to find an effective treatment.

These virtual sessions are here to show you that you are not alone, and to connect you with people who understand living with vitiligo and can signpost you to information and other support services.

The events are free to join, click the dates below to register:

Parent Support Network

The Parent Support Network is led by a small group of volunteers all of whom have children with vitiligo, or have personal experience of growing up with the condition.

The network exists to provide support for those who have questions or concerns relating to vitiligo, and to create a space where parents can feel supported and listened to.

Alongside the Facebook group listed at the top of this page, the group also host online events to give parents, carers and children a chance to say hello virtually. The events are free to join, and once confirmed, dates are posted below.

‘Vitil-i-go’ Meet Ups

Every month Dale and Courtney meet up to do a Park Run in London, and spread awareness about vitiligo. Recently they inspired Clare to do the same at her run in Aberdeen – and all three volunteers would love for you to join them!

You don’t need to be super fit, it’s a non-judgemental environment and lots of people walk the 5km course. It’s an opportunity to meet other people living with vitiligo, and bravely show your spots together. Events are free to join, but be sure to register at the Park Run website first. Dale, Courtney & Clare will be wearing Society t-shirts & looking our for you at the following events:

13th August – Old Deer Park, Richmond (London) & the Beach Esplanade (Aberdeen)

10th September – Bushy Park, Teddington (London)

15th October – Old Deer Park, Richmond (London) the Beach Esplanade (Aberdeen)

12th November – Bushy Park, Teddington (London) & the Beach Esplanade (Aberdeen)

10th December – Bushy Park, Teddington (London) & the Beach Esplanade (Aberdeen)

Email hello@vitiligosociety.org for more details or ask how to host your own meet up!

VitChat Live Chat Service

Our volunteer team are available to chat to live every Thursday evening. Our volunteers all have lived experience of vitiligo, so they understand how it feels to be diagnosed with the condition.

They will be available for you to message and to help signpost you to information such as vitiligo treatments, diet tips, camouflage or useful articles. Our volunteers are not trained medical professionals so they cannot advise on what treatment is right for you, but they can help you find information on the different options available for people living in the UK.

Visit our homepage to access the chat box every Thursday between 7-9pm: www.vitiligosociety.org

Our e-Newsletter

Did you know that we have a brilliant digital newsletter that brings you a roundup of all the vitiligo news, events and stories from the UK around the globe?

Sign up HERE for to subscribe to our mailing list to receive this and all our other vitiligo-related communications!