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Rare Disease

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This is Why You Should Never Trust an Armadillo
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This is Why You Should Never Trust an Armadillo

  • Post author:Lady Kehveen Abernathy
  • Post published:November 21, 2016
  • Post category:Hansen's disease/Rare Disease

Okay, yes, so this study was published in 2011, but time is obsolete, am I right? Especially when it comes to information as important as this. Listen closely. Remember leprosy?…

Continue Reading This is Why You Should Never Trust an Armadillo
Unfortunately, We Missed It

Unfortunately, We Missed It

  • Post author:Kathy Devanny
  • Post published:November 21, 2016
  • Post category:Acromegaly/Rare Disease/Timely

The physicians who left me undiagnosed said "we" missed the brain tumor. WE?! YOU, the 10 or 12 doctors I saw, missed that I had acromegaly. The doctor who finally…

Continue Reading Unfortunately, We Missed It
1 excelente motivo para llamar a esta chica hermosa anormal

1 excelente motivo para llamar a esta chica hermosa anormal

  • Post author:Patient Worthy Contributor
  • Post published:November 21, 2016
  • Post category:Cystinosis/Rare Disease

5 años de edad, Hadley Alexander no es normal. Cada mañana, su día comienza oficialmente a las 7 a.m. Ella convenció despierto por sus padres y, a través de un…

Continue Reading 1 excelente motivo para llamar a esta chica hermosa anormal
Han Llegado! 10 preguntas de un paciente con una Enfermedad Rara
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Han Llegado! 10 preguntas de un paciente con una Enfermedad Rara

  • Post author:Patient Worthy Contributor
  • Post published:November 20, 2016
  • Post category:Rare Disease

¿Alguna vez tiene alguna pregunta acerca de la quema de una enfermedad rara que te mueres por saber la respuesta? Nosotros también. Un montón de ellos. Es por eso que…

Continue Reading Han Llegado! 10 preguntas de un paciente con una Enfermedad Rara
10 consejos alimenticios para el Síndrome de Sjögren

10 consejos alimenticios para el Síndrome de Sjögren

  • Post author:Patient Worthy Contributor
  • Post published:November 19, 2016
  • Post category:Rare Disease/Sjogren's Syndrome

Para aquellos que tienen el síndrome de Sjögren, que no necesita toda la verdad. Pero para aquellos que no conocen, se asocia comúnmente con los ojos dos principales síntomas-secos y…

Continue Reading 10 consejos alimenticios para el Síndrome de Sjögren
Editor’s Choice: Dystonia Stories and Studies

Editor’s Choice: Dystonia Stories and Studies

  • Post author:Patient Worthy Contributor
  • Post published:November 18, 2016
  • Post category:Dystonia/Fabry Disease/Phenylketonuria/Rare Disease

Happy Pre-Thanksgiving Week Friends! It is almost Thanksgiving which is one of our FAVORITE holidays here at Patient Worthy. Why? Because on this holiday, we are focused on gratitude, family and…

Continue Reading Editor’s Choice: Dystonia Stories and Studies
A Boatload Of Missing Platelets Will Causes WHAT?
Source: commons.wikipedia.org

A Boatload Of Missing Platelets Will Causes WHAT?

  • Post author:Erica Zahn
  • Post published:November 18, 2016
  • Post category:Rare Disease/Thrombocytopenia

Immune thrombocytopenia purpura, or ITP, is a bleeding disorder caused by a lower than normal number of platelets, otherwise known as thrombocytes. Platelets are made in the bone marrow and when…

Continue Reading A Boatload Of Missing Platelets Will Causes WHAT?
Maybe You’ll Be Amazed When You Learn About Mastocytosis
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Maybe You’ll Be Amazed When You Learn About Mastocytosis

  • Post author:Erica Zahn
  • Post published:November 18, 2016
  • Post category:mastocytosis/Rare Disease

Mastocytosis is a rare immune disorder that is broken down into two categories: cutaneous (CM) systemic (SM) It affects men, women, and children in equal numbers. Children are more likely to have…

Continue Reading Maybe You’ll Be Amazed When You Learn About Mastocytosis
Why You Need to Be Aware of Your Pituitary Gland
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Why You Need to Be Aware of Your Pituitary Gland

  • Post author:Erica Zahn
  • Post published:November 18, 2016
  • Post category:Acromegaly/Rare Disease

When the pituitary gland overproduces growth hormone (GH), its usually because a pituitary adenoma has formed. An adenoma is a benign tumor that causes the patient to continue to grow. Hands and feet…

Continue Reading Why You Need to Be Aware of Your Pituitary Gland
In a Battle with Gaucher, This 12-Year-Old is #Winning

In a Battle with Gaucher, This 12-Year-Old is #Winning

  • Post author:James Ernest Cassady
  • Post published:November 18, 2016
  • Post category:Gaucher Disease/Rare Disease

Gaining 51 pounds in three years may not seem like a lot, but for Amber Mickley it meant doubling in size. When she was nine years old, Amber was small for…

Continue Reading In a Battle with Gaucher, This 12-Year-Old is #Winning
What Happens When Only Seven People in the World Have a Rare Disease?
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What Happens When Only Seven People in the World Have a Rare Disease?

  • Post author:Erica Zahn
  • Post published:November 18, 2016
  • Post category:Gorlin Chaudhry Moss syndrome/Rare Disease

Talk about rare diseases/ disorders/ conditions/ syndromes... there are only seven (SEVEN!!) documented cases of Gorlin Chaudhry Moss syndrome (GCM) in the world. All females. So, does as it come…

Continue Reading What Happens When Only Seven People in the World Have a Rare Disease?
Fabry Disease Clinical Trial, Balance
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Fabry Disease Clinical Trial, Balance

  • Post author:Kathy Devanny
  • Post published:November 18, 2016
  • Post category:Fabry Disease/Rare Disease

Fabry Disease is the number number two Lysosomal Storage disease in terms of numbers affected. It is an X-linked disease, with males passing on the mutated allele to all of their…

Continue Reading Fabry Disease Clinical Trial, Balance
Como ser un heroe a pesar de vivir con una enfermedad rara
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Como ser un heroe a pesar de vivir con una enfermedad rara

  • Post author:Patient Worthy Contributor
  • Post published:November 18, 2016
  • Post category:Dystonia/Rare Disease

Todos sabemos lo que es tener un mal día, una mala semana, o incluso un mal año. Pero la cosa es que, con el tiempo, las cosas suelen trabajar fuera;…

Continue Reading Como ser un heroe a pesar de vivir con una enfermedad rara
Baby Rosemary’s Plea

Baby Rosemary’s Plea

  • Post author:Rebekah
  • Post published:November 17, 2016
  • Post category:Ehlers-Danlos Syndrome/Rare Disease/Timely

Rare disease mom Bobbie recently had a new baby. While she is overjoyed at the latest addition to her family, she is fearing for her baby daughter's life. Her family…

Continue Reading Baby Rosemary’s Plea
Useful and Helpful Tips for Rare Polycythemia Vera
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Useful and Helpful Tips for Rare Polycythemia Vera

  • Post author:Sabina Kennedy
  • Post published:November 17, 2016
  • Post category:Myelodysplastic syndromes/Polycythemia vera/Rare Disease

Have you ever heard of polycythemia vera (PV)? Me neither, and that’s why I had to do some digging. There were quite a few facts that carried some heart-string shock…

Continue Reading Useful and Helpful Tips for Rare Polycythemia Vera
Fighting Rare Disease Pain the Cannabis Way
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Fighting Rare Disease Pain the Cannabis Way

  • Post author:Farrah Fontaine
  • Post published:November 17, 2016
  • Post category:Autoinflammatory Disease/Rare Disease/Timely

As more states open their arms to the wonders of marijuana (for medical purposes and for fun), they're also opening up a whole new way to look at treating rare…

Continue Reading Fighting Rare Disease Pain the Cannabis Way
This is the Kind of Appreciation Good Doctors and Nurses Deserve
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This is the Kind of Appreciation Good Doctors and Nurses Deserve

  • Post author:Lady Kehveen Abernathy
  • Post published:November 17, 2016
  • Post category:Primary Pulmonary Hypertension/Rare Disease

Here at Patient Worthy, we've written a few articles about misdiagnoses and how sometimes, doctors just aren't doing their jobs. But I think it's about time we honor the good…

Continue Reading This is the Kind of Appreciation Good Doctors and Nurses Deserve
An All-Too-Common Liver Disease May Soon Meet Its Match
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An All-Too-Common Liver Disease May Soon Meet Its Match

  • Post author:James Ernest Cassady
  • Post published:November 17, 2016
  • Post category:Nonalcoholic steatohepatitis/Rare Disease/Timely

In honor of liver awareness month, we've got some good news for people living with NASH, or nonalcoholic steatohepatitis. NASH is a kind of fatty-liver disease that is not connected to…

Continue Reading An All-Too-Common Liver Disease May Soon Meet Its Match
What to Know About Coordination of Rare Diseases at Sanford

What to Know About Coordination of Rare Diseases at Sanford

  • Post author:Patient Worthy Contributor
  • Post published:November 17, 2016
  • Post category:Rare Disease/Timely

Patient Worthy™ had the unique opportunity to talk to the Coordination of Rare Diseases at Sanford, or CoRDS. Check out the interview below. 1) Can you tell us a little about…

Continue Reading What to Know About Coordination of Rare Diseases at Sanford
La distonía cervical esta en tu imaginacion – Ahora asi es como lo manejas
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La distonía cervical esta en tu imaginacion – Ahora asi es como lo manejas

  • Post author:Patient Worthy Contributor
  • Post published:November 17, 2016
  • Post category:Dystonia/Rare Disease

Hay una famosa frase de Harry Potter y las reliquias de la muerte, cuando (* SPOILER ALERT *) Harry habla con el fantasma Dumbledore por última vez. Atrapado en un…

Continue Reading La distonía cervical esta en tu imaginacion – Ahora asi es como lo manejas
When Should You Not Take This Medicine as Prescribed?
Source: pixabay.com

When Should You Not Take This Medicine as Prescribed?

  • Post author:PW Blogger
  • Post published:November 16, 2016
  • Post category:Cystic Fibrosis/Rare Disease

When an arthritis medication can bring hope to so many more... Cystic fibrosis is a disease that affects the respiratory system and also the gastrointestinal system. There are 2 certain inflammasomes, called…

Continue Reading When Should You Not Take This Medicine as Prescribed?
How to Stay Strong When You Have EDS
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How to Stay Strong When You Have EDS

  • Post author:PW Blogger
  • Post published:November 16, 2016
  • Post category:Ehlers-Danlos Syndrome/Rare Disease

How would you respond if your body did not work for you but against you? What if you felt that your body was actually your enemy? For people with Ehlers-Danlos…

Continue Reading How to Stay Strong When You Have EDS
Fabry Disease: Three Cheers for Unrelenting Scientists Fighting for a Cure
[Source: Pixabay.com]

Fabry Disease: Three Cheers for Unrelenting Scientists Fighting for a Cure

  • Post author:Alisha Stone
  • Post published:November 16, 2016
  • Post category:Fabry Disease/Rare Disease

I read a report recently from the New England Journal of Medicine about a clinical trial and thought I’d share it with you because it’s about Fabry disease, a genetic disease…

Continue Reading Fabry Disease: Three Cheers for Unrelenting Scientists Fighting for a Cure
What Can This Stunning Musician Show You About Parkinson’s?
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What Can This Stunning Musician Show You About Parkinson’s?

  • Post author:Erica Zahn
  • Post published:November 16, 2016
  • Post category:Multiple system atrophy (MSA)/Parkinson's Disease/Rare Disease

When I hear the word Parkinson's, the first image that comes to mind is a long-haired guitar player on stage, captivating the hundreds of people who'd come to hear his…

Continue Reading What Can This Stunning Musician Show You About Parkinson’s?
Wanted: More Brilliant Professors to Dumb Down Hemophilia
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Wanted: More Brilliant Professors to Dumb Down Hemophilia

  • Post author:Alisha Stone
  • Post published:November 16, 2016
  • Post category:Hemophilia A/Hemophilia B/Rare Disease

Shocker! Did you know it’s possible to acquire hemophilia? There’s a professor who I’m obsessed with from Texas—that would be “obsessed” as in a healthy obsession! And here’s why: He…

Continue Reading Wanted: More Brilliant Professors to Dumb Down Hemophilia
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The Mentor She Wished She Had - How Elizabeth Became a Lifeline for EB
Finding Strength Together: Scott and Katie’s Journey with Advanced Kidney
You Are Not Alone: Empowering the Advanced Kidney Cancer Community
Finding Light Through Story-The Power of Ambassadorship in the Endometrial Cancer Community
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