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A 12-Year-Old Blogs His Experience with Idiopathic Intracranial Hypertension
Photo by Francisco Gonzalez on Unsplash

A 12-Year-Old Blogs His Experience with Idiopathic Intracranial Hypertension

  • Post author:Jessica Lynn
  • Post published:May 19, 2020
  • Post category:Intracranial Hypertension

A few years ago, Kyan Harris started experiencing some unwelcome health issues. At just nine years old, the boy wanted to play rugby with his friends. But instead, he was…

Continue Reading A 12-Year-Old Blogs His Experience with Idiopathic Intracranial Hypertension
Kristie’s Story Part 2:  Adjusting After the Diagnosis

Kristie’s Story Part 2: Adjusting After the Diagnosis

  • Post author:Rebekah
  • Post published:May 19, 2020
  • Post category:Rare Disease/Refsum Disease

To read part 1 click here Kristie’s medical mystery was now solved.  What was the next step?  After speaking with her genetic counselor about her results, Kristie was referred to…

Continue Reading Kristie’s Story Part 2: Adjusting After the Diagnosis
Kristie’s Story Part 1: Journey to a Diagnosis

Kristie’s Story Part 1: Journey to a Diagnosis

  • Post author:Rebekah
  • Post published:May 18, 2020
  • Post category:Rare Disease/Refsum Disease

Kristie DeMarco was an extreme athlete- constantly training for triathlons, ironman races, ice swimming, and open water swimming. She loved to compete in various feats of strength and endurance. Overall,…

Continue Reading Kristie’s Story Part 1: Journey to a Diagnosis
Hemophilia and COVID-19: Addressing the Great Unknown
source: pixabay.com

Hemophilia and COVID-19: Addressing the Great Unknown

  • Post author:Jessica Lynn
  • Post published:May 11, 2020
  • Post category:COVID-19/Hemophilia

When Shellye Horowitz was younger, she had a clear link to the rare disease community: her father. He had hemophilia and, much like many patients, relied on blood clotting factor…

Continue Reading Hemophilia and COVID-19: Addressing the Great Unknown
Raising a Daughter with CHARGE Syndrome: Jessica Lechuga’s Story

Raising a Daughter with CHARGE Syndrome: Jessica Lechuga’s Story

  • Post author:Jessica Lynn
  • Post published:May 8, 2020
  • Post category:CHARGE syndrome/Rare Disease

According to UIC Today, Jessica Lechuga became immersed within the rare disease community when she was still a teenager. That's because, at age 17, Jessica gave birth to her daughter…

Continue Reading Raising a Daughter with CHARGE Syndrome: Jessica Lechuga’s Story
Maddie’s Story: Living with Wiedemann Steiner Syndrome

Maddie’s Story: Living with Wiedemann Steiner Syndrome

  • Post author:Kendall Mason
  • Post published:May 2, 2020
  • Post category:Rare Disease

Maddie Nordhoy has a smile that can light up the room. She constantly brings joy to those around her, especially her family. In fact, she is even the inspiration for…

Continue Reading Maddie’s Story: Living with Wiedemann Steiner Syndrome
Interviewing Your Future Self
source: pixabay.com

Interviewing Your Future Self

  • Post author:Patient Worthy Contributor
  • Post published:May 1, 2020
  • Post category:Cystinosis

Because I will be looking for a job from a rare but certainly not unique place of being, I decided to reach out to a mentor who lives with the…

Continue Reading Interviewing Your Future Self
NJ Boy with Castleman Disease Returns Home After “Largest Mass Ever” Removed
source: pixabay.com

NJ Boy with Castleman Disease Returns Home After “Largest Mass Ever” Removed

  • Post author:Jessica Lynn
  • Post published:April 29, 2020
  • Post category:Castleman Disease/Rare Disease

10-year-old Joey Koslowski doesn't let the small...err, the big stuff get him down. According to MyCentralJersey, the boy is "the youngest child to have the largest mass in the world" caused…

Continue Reading NJ Boy with Castleman Disease Returns Home After “Largest Mass Ever” Removed
How to Find Meaning and Purpose Even When You’re Suffering: Q&A with Tom Seaman, Health Coach
source: pixabay.com

How to Find Meaning and Purpose Even When You’re Suffering: Q&A with Tom Seaman, Health Coach

  • Post author:Tom Seaman
  • Post published:February 18, 2020
  • Post category:Dystonia

I recently had the pleasure of being interviewed by Sunshine Mugrabi about how I transformed my life over the past 20 years in the face of immense pain and suffering…

Continue Reading How to Find Meaning and Purpose Even When You’re Suffering: Q&A with Tom Seaman, Health Coach
How to Support a Friend or Family Member Dealing with a Rare Disease Diagnosis

How to Support a Friend or Family Member Dealing with a Rare Disease Diagnosis

  • Post author:Octavia Walker
  • Post published:November 27, 2019
  • Post category:Chiari Malformation/Rare Disease

I have been writing for this website for a little over 2 years. Neatly collecting, reading, and reporting on stories of people with rare conditions and disabilities. Little did I…

Continue Reading How to Support a Friend or Family Member Dealing with a Rare Disease Diagnosis
Battling Behcet’s and Building a Community

Battling Behcet’s and Building a Community

  • Post author:Rebekah
  • Post published:October 21, 2019
  • Post category:Behçet's

Sarah experienced her first symptoms at age eight. She suffered frequent and long migraines, despite being so young. Doctors were concerned she may have meningitis but never got to the…

Continue Reading Battling Behcet’s and Building a Community
A Parental Odyssey of Rare Disease

A Parental Odyssey of Rare Disease

  • Post author:Patient Worthy Contributor
  • Post published:October 8, 2019
  • Post category:Rare Disease

“I have cried a lot more in the last ten years of my life than ever before.”  A parental odyssey of rare disease, in two of their three children, and…

Continue Reading A Parental Odyssey of Rare Disease
“I have been in the trenches. I know what it’s like to rise back up”: Beth’s Behcet’s Story

“I have been in the trenches. I know what it’s like to rise back up”: Beth’s Behcet’s Story

  • Post author:Rebekah
  • Post published:August 8, 2019
  • Post category:Behçet's/Rare Disease

At just nineteen, Beth often didn’t feel well and regularly had a sickly pallor. When she went to a doctor, the doctor dismissed her and told her she just needed…

Continue Reading “I have been in the trenches. I know what it’s like to rise back up”: Beth’s Behcet’s Story
Coming Through the Darkness: a Blepharospasm Story

Coming Through the Darkness: a Blepharospasm Story

  • Post author:Patient Worthy Contributor
  • Post published:July 31, 2019
  • Post category:Blepharospasm/Rare Disease

Talking about mental illness is never easy but I wanted to share my experience of it with you. In my case, it came as part of my struggle with Benign…

Continue Reading Coming Through the Darkness: a Blepharospasm Story
Living with Blepharospasm. Validating your Sense of Purpose.

Living with Blepharospasm. Validating your Sense of Purpose.

  • Post author:Patient Worthy Contributor
  • Post published:June 21, 2019
  • Post category:Blepharospasm/Rare Disease

Adapting to a long- term health condition, is not an easy road to be on. There are many phases we go through during our journey from denial to acceptance. It…

Continue Reading Living with Blepharospasm. Validating your Sense of Purpose.
Rare Inspiration: A Myasthenia Gravis Patient Story

Rare Inspiration: A Myasthenia Gravis Patient Story

  • Post author:Patient Worthy Contributor
  • Post published:May 10, 2019
  • Post category:Myasthenia Gravis/Rare Disease

As I listened to her story I kept thinking, “You can’t make this stuff up.” Or at least no one would want to anyway. The first time I met Adeola…

Continue Reading Rare Inspiration: A Myasthenia Gravis Patient Story
Tessa’s Tenacity: an Acromegaly Journey

Tessa’s Tenacity: an Acromegaly Journey

  • Post author:Rebekah
  • Post published:April 25, 2019
  • Post category:Acromegaly/Rare Disease

In 2012 Tessa noticed a gap between her front teeth. She was a little confused. She had had braces when she was younger and her teeth hadn’t had any gaps…

Continue Reading Tessa’s Tenacity: an Acromegaly Journey
Lisa Deck’s Journey Part 1

Lisa Deck’s Journey Part 1

  • Post author:Rebekah
  • Post published:January 17, 2019
  • Post category:Moyamoya Disease/Rare Disease

At age twenty one, Lisa was about to graduate college and had a promising future career in front of her. All that was left was graduation itself. The week before…

Continue Reading Lisa Deck’s Journey Part 1
Heidi Jo’s Familial Chylomicronemia Syndrome Story
Heidi Jo in her days of service.

Heidi Jo’s Familial Chylomicronemia Syndrome Story

  • Post author:Kathy Devanny
  • Post published:January 15, 2019
  • Post category:Familial Chylomicronemia Syndrome

Heidi Jo Price, beautiful and brave, has jumped out of airplanes with a pack on her back as a member of the 173 Airborne Brigade Combat Team. What brought this…

Continue Reading Heidi Jo’s Familial Chylomicronemia Syndrome Story
Veronika’s Story of Living with Gastroparesis Will Inspire You
Source: Pixabay

Veronika’s Story of Living with Gastroparesis Will Inspire You

  • Post author:Samuel Sachs
  • Post published:September 7, 2017
  • Post category:Gastroparesis

Veronika was diagnosed with gastroparesis as a young girl. The cause was unknown. Her symptoms were demoralizing. Veronika found ways to stay positive and combat her illness. Read more below,…

Continue Reading Veronika’s Story of Living with Gastroparesis Will Inspire You
Vea cómoa un médico experto le cambio la vida a este hombre

Vea cómoa un médico experto le cambio la vida a este hombre

  • Post author:Patient Worthy Contributor
  • Post published:January 5, 2017
  • Post category:CVID/Rare Disease

En esta cuenta, desde Philly.com, el Dr. Thomas Klein, alergólogo e inmunólogo, describe su problema. Un misterio se había encontrado en su camino que no se creía capaz de resolver.…

Continue Reading Vea cómoa un médico experto le cambio la vida a este hombre
Meet a Huntington’s Advocate Fighting for Family

Meet a Huntington’s Advocate Fighting for Family

  • Post author:Rebekah
  • Post published:February 24, 2016
  • Post category:Huntington's disease

Meet an incredible advocate for Huntington’s disease. Chasity Boatman grew up witnessing the tragic effects of this degenerative and fatal disease first hand and has now become a dedicated and…

Continue Reading Meet a Huntington’s Advocate Fighting for Family
NOMID or Not, This Young Woman is Going Strong

NOMID or Not, This Young Woman is Going Strong

  • Post author:Rebekah
  • Post published:January 6, 2016
  • Post category:CAPS/Neonatal onset multisystem inflammatory disease/Rare Disease

Janelle is a 21 year old student at the University of Nebraska at Kearney. She has a great sense of humor, has shown horses for years and someday she wants…

Continue Reading NOMID or Not, This Young Woman is Going Strong

See How An Expert Doctor Changed This Man’s Life

  • Post author:Patient Worthy Contributor
  • Post published:October 19, 2015
  • Post category:CVID/Rare Disease

In this account, from Philly.com, Dr. Thomas Klein, allergist and immunologist, describes his problem.  A mystery had come across his path that he didn't think he could solve. He was seeing…

Continue Reading See How An Expert Doctor Changed This Man’s Life
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