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The Family of Actor Bruce Willis Acknowledges his Diagnosis of Primary Progressive Aphasia

The Family of Actor Bruce Willis Acknowledges his Diagnosis of Primary Progressive Aphasia

  This week the family of actor Bruce Willis announced that he received a diagnosis of frontotemporal dementia (FTD), a rare disease that causes behavioral changes, language, speech, and memory…

Continue Reading The Family of Actor Bruce Willis Acknowledges his Diagnosis of Primary Progressive Aphasia
EA-2353 for Retinitis Pigmentosa (RP) Granted Fast Track Designation

EA-2353 for Retinitis Pigmentosa (RP) Granted Fast Track Designation

  In the United States, Fast Track designation is granted to drugs designed to treat rare and/or serious conditions and that fill an unmet medical need. The process aims to…

Continue Reading EA-2353 for Retinitis Pigmentosa (RP) Granted Fast Track Designation
New AI Technology Connects Avatar and Friedreich’s Ataxia

New AI Technology Connects Avatar and Friedreich’s Ataxia

Dr. Valeria Ricotti of the Institute for Child Health- Great Ormond Street UK, spoke with BBC News on the subject of AI analyzing body movement. Dr. Ricotti and other researchers…

Continue Reading New AI Technology Connects Avatar and Friedreich’s Ataxia
Parents Play a Vital Role in the Struggle Against Rare Disease

Parents Play a Vital Role in the Struggle Against Rare Disease

The number of identified rare diseases continues to climb every year, with the number recently reaching the 11,000+ mark. Some of them have only a handful of identified cases, and…

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JAYPIRCA is Now FDA-Approved for Mantle Cell Lymphoma (MCL) Treatment

JAYPIRCA is Now FDA-Approved for Mantle Cell Lymphoma (MCL) Treatment

  For many people living with mantle cell lymphoma (MCL), the standards-of-care include Bruton's tyrosine kinase (BTK) inhibitors. But there is a subset of patients who do not respond well,…

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Could SGSH Enzyme Replacement Therapy Benefit Children with MPS III-A?

Could SGSH Enzyme Replacement Therapy Benefit Children with MPS III-A?

  Enzyme replacement therapy (ERT) has been explored as a potential therapeutic option for mucopolysaccharidosis type III A (MPS III-A or Sanfilippo syndrome type A). However, these solutions have not…

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ICYMI: Positive Topline Data Available on Pemvidutide for NAFLD

ICYMI: Positive Topline Data Available on Pemvidutide for NAFLD

  In a late December 2022 news release from biopharmaceutical company Altimmune, Inc., the company shared that positive topline data was available from a 24-week study—including a 12-week extension—which evaluated…

Continue Reading ICYMI: Positive Topline Data Available on Pemvidutide for NAFLD
Informing Treatment Decisions for Psoriatic Arthritis: A Discussion with Dr. Soumya Chakravarty

Informing Treatment Decisions for Psoriatic Arthritis: A Discussion with Dr. Soumya Chakravarty

From November 10-14, 2022, various stakeholders within the rheumatology sphere connected at the American College of Rheumatology’s (ACR) Convergence 2022. During ACR Convergence, described as the world’s premier rheumatology experience,…

Continue Reading Informing Treatment Decisions for Psoriatic Arthritis: A Discussion with Dr. Soumya Chakravarty
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Finding Light Through Story-The Power of Ambassadorship in the Endometrial Cancer Community
*cancer that cannot be removed with surgery or has spread to other parts of the body. GEJ= gastroesophageal junction (where the esophagus joins the stomach)
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