Vitiligo Association of Uganda

Myth about vitiligo and the fact Being burnt by twin is a myth that shows up in a lot of communities, especially in parts of Africa. I know people mean it when they’re trying to explain something they don’t understand, but it’s not true at all. #vitiligoAwareness #June

Together we can end the stigma of people living with vitiligo, thank you @VAUorg for the initiative

What’s one thing about vitiligo no one warned you about? For me? The emotional rollercoaster. The grieving. The “good skin days vs bad mental health days”. #VitiligoCommunity #BeyondJustMySkin #VAU

Persons with albinism are speaking out against harmful myths that link them to wealth through witchcraft. As @albinismumbrell ED Olive Namutebi notes, if these claims were true, why do many persons with albinism still face poverty & exclusion? Let's reject myths & embrace facts.

@rctnjeru @AchanDianah3 @AaronKeyster @AkugizibweRodg6 @EvansNiwam64148 @gloriabae01 @Esau_Matsiko @karothk256 @iamarnoldworld @KwikirizaNova @MrInfluencerUg1 @Nabimara_Paul You are most welcome dear

@AchanDianah3 @VAUorg @AaronKeyster @AkugizibweRodg6 @EvansNiwam64148 @gloriabae01 @Esau_Matsiko @karothk256 @iamarnoldworld @KwikirizaNova @MrInfluencerUg1 @Nabimara_Paul Very essential in ending the stigma our brothers and sisters go through. Thank you @VAUorg

Join us end the stigma of people living with vitiligo, it's just a skin condition, it's not contagious, it's not HIV/AIDS, it's not Leprosy neither were we burnt by twins @VAUorg

2. Patches deserve sunscreen + respect 3. Everyone deserves to feel proud in their skin Look at those smiles. That’s what happens when fear leaves the room. #VAU #CommunityOutreach #BeyondJustMySkin #EndVitiligoStigma

It’s showing up. It’s answering questions. It’s letting kids see that vitiligo is not a curse, not contagious, not a reason to hide. VAU’s vision: “A stigma-free, healthy and empowered community of persons living with and affected by vitiligo.”

Vitiligo is just skin. It doesn’t define her. It doesn’t limit her. Holding sunscreen = holding her power back. Standing in uniform = standing in confidence. This is why we do the work. For her. For all of them. 1. Vitiligo is not contagious

Today, we took one more step toward that vision. If we teach them young, they’ll grow up without stigma. She used to hide her face. Today she’s smiling for the camera. That’s what happens when kids are taught the truth early:

Today, together with @LftWUG , we reflected on our learning & documentation journey under the #WeCanWork program, sharing lessons learned & best practices from our advocacy efforts. The program has trained 40+ young advocates across Mukono,Wakiso, Kampala & Gulu, 12+ mainstream.

It’s science. So if you see someone with patches around their eyes or mouth, now you know why. And no, it’s not contagious. It’s not poor hygiene. It’s just how vitiligo works. Knowledge kills stigma. #Endstigma #June #VitiligoAwareness

“Vitiligo’s Favorite Spots”* Did you know vitiligo has favorite places to show up? Dermatologists call them “moist areas” or “areas of friction”. That’s why you’ll often see it around 👁️ Eyes & eyelids 👄 Lips & mouth corners 👃 Nostrils 🖐️ Fingers & wrists 🦶 Toes & feet

💪 Armpits, elbows, knees Plus anywhere skin rubs together or gets injured Melanocytes - the cells that give skin color - are more sensitive in these spots. Stress, friction, sunburn, or even small cuts can “trigger” vitiligo there first. It’s not random.

So don't stop at "What happened to your skin?" Ask, "What's your story?" You might discover what I've learned: people are always more interesting than the thing you noticed first. Because I am more than my patches. And so is everyone else.

My shirt says Beyond Just My Skin and honestly, that's how I live every day. Yes, you'll probably notice the vitiligo first. The patches do tend to introduce themselves before I do. But that's only one part of my story. #VitiligoAwareness #MoreThanPatches #EndTheStigma

I'm a daughter, a friend, an advocate, a dreamer, and a woman with ambitions far bigger than my skin. I laugh, I learn, I hustle, I heal, and I keep showing up. Vitiligo is what you see. Strength is who I am. Purpose is what drives me.

The only gift I request you is to push me to 10k before world vitiligo day and follow @VAUorg for vitiligo updates

He should visit the dermatologists if he is diagnosed with vitiligo, then he should join our association @VAUorg ,

So no, it’s not “inherited like eye color”. And no, it’s not a reason to discriminate in marriage, jobs, or school. #VitiligoFacts #GeneticsExplained #NoMoreMyths #VitiligoAwareness

*The truth about genetics and vitiligo vitiligo:* 1. *Genes play a role* - If your parent/sibling has it, your risk is a bit higher. About 20-30% of people with vitiligo have family history.

Most people with the genes never develop a single patch. It’s like having a light switch in your house. The switch exists, but the light only comes on if something flips it. Stress, injury, illness can flip it. Sometimes nothing flips it at all.

Why the myth hurts:* People hear “genetic” and think “my fault” or “don’t marry them, kids will get it”. That’s stigma talking, not science. Vitiligo can have a genetic link. About 1 in 4 people with vitiligo have a family member with it.