NFL Player Tevin Coleman Discusses Daughter’s Sickle Cell Disease (SCD) Diagnosis
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NFL Player Tevin Coleman Discusses Daughter’s Sickle Cell Disease (SCD) Diagnosis

  On the field, Running Back (RB) Tevin Coleman has done some amazing things. He has played in 94 games, gained 3,319 rushing yards, and scored 25 touchdowns. Off the…

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“A Rare Gem”: Savannah’s Story Spreads Ogden Syndrome Awareness (Pt. 1)
Photo courtesy of Lacey Smith

“A Rare Gem”: Savannah’s Story Spreads Ogden Syndrome Awareness (Pt. 1)

Right now, there are approximately 100 people in the world who have been diagnosed with Ogden syndrome, a rare neurodevelopmental disorder. Lacey Smith’s 11-year-old daughter Savannah is part of this…

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Managing a Dual Diagnosis: How Sarah has Survived, and Overcome, Challenges from Addison’s Disease and Stiff Person Syndrome (Pt. 2)
Photo Courtesy of Sarah Maxwell

Managing a Dual Diagnosis: How Sarah has Survived, and Overcome, Challenges from Addison’s Disease and Stiff Person Syndrome (Pt. 2)

Before you read on, make sure to check out Part 1 of Sarah's story. In Part 1, Sarah discusses the traumatic (and life-threatening!) odyssey that led to her eventual Addison's disease diagnosis…

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Study of the Week: BPTA Syndrome Research Uncovers Hereditary Disease Mechanism that Could help Prevent Cancer
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Study of the Week: BPTA Syndrome Research Uncovers Hereditary Disease Mechanism that Could help Prevent Cancer

Welcome to Study of the Week from Patient Worthy. In this segment, we select a study we posted about from the previous week that we think is of particular interest…

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Managing a Dual Diagnosis: How Sarah Has Survived, and Overcome, Challenges from Addison’s Disease and Stiff Person Syndrome (Pt. 1)
Photo Courtesy of Sarah Maxwell

Managing a Dual Diagnosis: How Sarah Has Survived, and Overcome, Challenges from Addison’s Disease and Stiff Person Syndrome (Pt. 1)

When Sarah Williams Maxwell was 18 months old, she was diagnosed with type 1 diabetes (T1D). Outside of managing this condition, Sarah was relatively healthy until 2014, when her diagnostic…

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The Extremely Rare Disease BPTA Syndrome may Lead Scientists to Prevent the Development of Cancer
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The Extremely Rare Disease BPTA Syndrome may Lead Scientists to Prevent the Development of Cancer

  The Schleswig-Holstein University Hospital and the Max Planck Institute in Germany have investigated a hereditary condition that is extremely rare called brachyphalangy, polydactyly, and tibial aplasia/hypoplasia (BPTA) syndrome. Symptoms…

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Tethered Spinal Cord, Dermal Sinus Tract, and Chiari Malformation: How Kayden’s Health Journey Inspired his Mother to Take Action (Pt. 2)
Photo courtesy of Kristin and Matt Lashoff

Tethered Spinal Cord, Dermal Sinus Tract, and Chiari Malformation: How Kayden’s Health Journey Inspired his Mother to Take Action (Pt. 2)

Before you read on, make sure to check out Part 1 of Kristin and Kayden's story. In Part 1, Kristin discusses the diagnostic journey and how Kayden was diagnosed with a dermal…

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Tethered Spinal Cord, Dermal Sinus Tract, and Chiari Malformation: How Kayden’s Health Journey Inspired his Mother to Take Action (Pt. 1)
Credit: Alexandria Mooney Photography

Tethered Spinal Cord, Dermal Sinus Tract, and Chiari Malformation: How Kayden’s Health Journey Inspired his Mother to Take Action (Pt. 1)

The Lashoff family loves living in St. Louis; they’ve been there for six years and can’t get enough of it, from watching hockey at the Enterprise Center to marveling at…

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Fighting for Recognition: Why Kate Continues to Advocate for PTEN Hamartoma Tumor Syndrome Awareness
Photo courtesy of Kate Turner

Fighting for Recognition: Why Kate Continues to Advocate for PTEN Hamartoma Tumor Syndrome Awareness

A rare disease diagnosis can conjure up a multitude of emotions, from relief at finally learning what is going on to fear or isolation when trying to figure out what…

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