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July 1, 2025 Comments Off

Despite their distinct medical causes, albinism and vitiligo are often grouped in the public eye, not because they are the same, but because society responds to them in similar ways. Both conditions affect skin pigmentation,

June 14, 2025 Comments Off

Massé World proudly joins the global vitiligo community in observing World Vitiligo Day. This year’s event will be hosted in Tampa, Florida, and will be more than a celebration. With a focus on

May 29, 2025 Comments Off

Empowering Difference. Celebrating Dignity.Massé World proudly joins the global community in observing International Albinism Awareness Day (IAAD) on June 13, 2025, under the newly announced theme: “Demanding our rights: Protect our skin, Preserve

May 29, 2025 Comments Off

The 2025 Coalition for Skin Diseases (CSD) Hill Day, held from May 18 to 20 in Washington, D.C., united over 75 patient advocates, healthcare professionals, and nonprofit organizations to champion the needs of

May 10, 2025 Comments Off

– Audrey Krupala –My Name is Audrey Krupala. I’m a wife, mother, friend, daughter, and realtor. I’m 35 years old, and I’ve lived with vitiligo since I was 9. Growing up with this

April 12, 2025 Comments Off

The BIO International Convention will take place from June 16-19, 2025, at the Boston Convention and Exhibition Center. This event is the largest and most comprehensive gathering for biotechnology, expected to host 20,000

March 16, 2025 Comments Off

Chronic skin conditions are often impossible to ignore. Their visibility draws attention, but paradoxically, those affected often feel invisible. Despite the profound impact these diseases have, many patients are left without the recognition

March 5, 2025 Comments Off

BEN BROWN: A STORY OF PURE RESILIENCEMy name is Arthur Benjamin Brown, though my friends call me Brother Ben, and I am reaching out to you with a personal story and an important

February 24, 2025 Comments Off

The FDA’s Rare Disease Innovation Hub (Hub) has released its Strategic Agenda, detailing its first-year actions and engagement with the rare disease community while clarifying its structure and programs. The Hub fosters collaboration

February 13, 2025 Comments Off

My name is Meshack Sisenda, and I was born and raised in Kitale, Trans-Nzoia County, Kenya. I am the only child with albinism in a family of three children, raised by a single

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