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Monthly Archives: October 2016

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The Best News for Behcet’s Treatment in a Long Time
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The Best News for Behcet’s Treatment in a Long Time

  • Post author:Farrah Fontaine
  • Post published:October 27, 2016
  • Post category:Behçet's/Panuveitis

One of the (many) issues with having Behcet's disease is that very few of the medications we use on a daily basis have ever been studied in people with our…

Continue Reading The Best News for Behcet’s Treatment in a Long Time
¿Necesita ayuda manejando una enfermedad rara? Hay una aplicación para eso
Pixabay

¿Necesita ayuda manejando una enfermedad rara? Hay una aplicación para eso

  • Post author:Patient Worthy Contributor
  • Post published:October 27, 2016
  • Post category:Rare Disease

La tecnología actual nos está llevando a nuevas (in)cómodas alturas, a un ritmo que pocos les sorprenderia. Para aquellos que están viviendo con la narcolepsia, este avión no tripulado de…

Continue Reading ¿Necesita ayuda manejando una enfermedad rara? Hay una aplicación para eso
Let’s Get Down and Dirty with Aplastic Anemia
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Let’s Get Down and Dirty with Aplastic Anemia

  • Post author:Alisha Stone
  • Post published:October 26, 2016
  • Post category:Aplastic anemia/Rare Disease

Here’s some down and dirty information about aplastic anemia, an autoimmune disease that results when the body cannot produce life-sustaining bone marrow, and doesn't create enough red and white blood cells and platelets.…

Continue Reading Let’s Get Down and Dirty with Aplastic Anemia
CGD And IBD: How to Solve Your Health Problems
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CGD And IBD: How to Solve Your Health Problems

  • Post author:Erica Zahn
  • Post published:October 26, 2016
  • Post category:CGD/Rare Disease

Chronic granulomatous disease (CGD) is a genetic condition that affects the immune system. It's in the family of primary immuno-deficiencies, and makes it hard for the body to fight infections…

Continue Reading CGD And IBD: How to Solve Your Health Problems
If You Have EDS, You Need to Know About This Before You See the Dentist

If You Have EDS, You Need to Know About This Before You See the Dentist

  • Post author:Farrah Fontaine
  • Post published:October 26, 2016
  • Post category:Ehlers-Danlos Syndrome/Rare Disease

How many people don't like going to the dentist? A lot. And how many people with Ehlers-Danlos Syndrome (EDS) hate going to the dentist? Most of them. Or at least…

Continue Reading If You Have EDS, You Need to Know About This Before You See the Dentist
Suspect You Have Cushing’s Disease? 5 Critical Things You Need to Know
[Source: Pixabay.com]

Suspect You Have Cushing’s Disease? 5 Critical Things You Need to Know

  • Post author:Alisha Stone
  • Post published:October 26, 2016
  • Post category:Cushing Disease

Suspect You May Have Cushing’s Disease? Read On Now! If you suspect that you might have Cushing’s disease because you have some of the following symptoms, you DEFINITELY need to…

Continue Reading Suspect You Have Cushing’s Disease? 5 Critical Things You Need to Know
My “Anxiety Disorder” May Be Something Else Completely?
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My “Anxiety Disorder” May Be Something Else Completely?

  • Post author:PW Blogger
  • Post published:October 26, 2016
  • Post category:Dysautonomia/POTS/Rare Disease

One day you go from being an active person full of life to waking up not feeling like yourself. You get a bad cold. You never seem to bounce back.…

Continue Reading My “Anxiety Disorder” May Be Something Else Completely?
Stories of Courage Like This One Should be Mainstream

Stories of Courage Like This One Should be Mainstream

  • Post author:Alisha Stone
  • Post published:October 26, 2016
  • Post category:Aplastic anemia/Rare Disease

During one of those “dog days of summer,” I was searching around for some inspiration; I’d been feeling blue because a friend of mine, who is in her 50s and…

Continue Reading Stories of Courage Like This One Should be Mainstream
Skip That Starbucks and Help Out This 6 Year Old Girl
[Source: pixabay.com]

Skip That Starbucks and Help Out This 6 Year Old Girl

  • Post author:Erica Zahn
  • Post published:October 26, 2016
  • Post category:Aplastic anemia/Rare Disease/Timely

The human body is a magnificent machine, and each cell has a role to play. In a way, it's like a jigsaw puzzle that ordinarily is put together perfectly. The only…

Continue Reading Skip That Starbucks and Help Out This 6 Year Old Girl
La narcolepsia 101: Para el recién diagnosticado

La narcolepsia 101: Para el recién diagnosticado

  • Post author:Patient Worthy Contributor
  • Post published:October 26, 2016
  • Post category:Narcolepsy

Si no te has dado cuenta, Patient worthy ha escrito bastante sobre la narcolepsia. Sin embargo, no podemos dejar de pensar que dar un paso atrás para responder a algunas…

Continue Reading La narcolepsia 101: Para el recién diagnosticado
Promising Change for Improved Rare Pompe Detection
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Promising Change for Improved Rare Pompe Detection

  • Post author:Sabina Kennedy
  • Post published:October 25, 2016
  • Post category:Pompe Disease/Rare Disease

Are you ready to start a family? Or are you considering adding another child to your nest? If so, the March of Dimes shares some insight on what moms or…

Continue Reading Promising Change for Improved Rare Pompe Detection
How to Party Hard for Dysautonomia Awareness
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How to Party Hard for Dysautonomia Awareness

  • Post author:James Ernest Cassady
  • Post published:October 25, 2016
  • Post category:Dysautonomia/Rare Disease/Timely

Looking for a way to celebrate Dysautonomia Awareness month this year? Then you need to check out Dysautonomia International. Why? Because this incredible organization provides wonderful support to the dysautonomia community…

Continue Reading How to Party Hard for Dysautonomia Awareness
Why is it Important to Screen Your Baby for CPT II? 
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Why is it Important to Screen Your Baby for CPT II? 

  • Post author:Erica Zahn
  • Post published:October 25, 2016
  • Post category:Carnitine palmitoyl transferase 2 deficiency/Rare Disease

Carnitine palmitoyltransferase II deficiency (CPT II) is a long-winded way of describing a fatty acid oxidation disorder that prevents the body from using fat. It's caused by enzymes  that aren't properly functioning,…

Continue Reading Why is it Important to Screen Your Baby for CPT II? 
How Important is it for Your Doctor to Believe You?
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How Important is it for Your Doctor to Believe You?

  • Post author:James Ernest Cassady
  • Post published:October 25, 2016
  • Post category:Dysautonomia/Rare Disease

In this article, Dr. Richard Fogoros examines the past and present of dysautonomia while also offering some hope for the future. Among his observations: the condition is far from new,…

Continue Reading How Important is it for Your Doctor to Believe You?
Giving Tricks or Treats This Halloween?

Giving Tricks or Treats This Halloween?

  • Post author:Kristen Lord
  • Post published:October 25, 2016
  • Post category:Rare Disease

Are you planning on handing out candy for Halloween? If so I have a suggestion for you! This is the perfect opportunity for you to advocate for the rare disease…

Continue Reading Giving Tricks or Treats This Halloween?
Angie’s Message on the Power of Positivity
https://pixabay.com/en/youth-active-jump-happy-sunrise-570881/

Angie’s Message on the Power of Positivity

  • Post author:Patient Worthy Contributor
  • Post published:October 25, 2016
  • Post category:Rare Disease

PW Contributor Angie just blogged about one of the most important messages us in the rare disease world need to hear: The Power of Positivity. Read more below: Positivity is hands…

Continue Reading Angie’s Message on the Power of Positivity
How to Take the Headache Out of Dystonia
Source: www.pixabay.com

How to Take the Headache Out of Dystonia

  • Post author:Sabina Kennedy
  • Post published:October 25, 2016
  • Post category:Dystonia/Rare Disease

Who doesn’t love a good story? A story that speaks to us. A story that spins a negative into a positive. When I listen to a person tell a story, I…

Continue Reading How to Take the Headache Out of Dystonia
Do You Know How to Talk to Aplastic Anemia Experts?
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Do You Know How to Talk to Aplastic Anemia Experts?

  • Post author:EmpatheticBadass
  • Post published:October 25, 2016
  • Post category:Aplastic anemia/Myelodysplastic syndromes/paroxysmal nocturnal hemoglobinuria/Rare Disease/Timely

Wouldn’t it be nice if you could talk to one of those “nationally known” specialists about your aplastic anemia? Well, if you can make it to West Palm Beach, Florida…

Continue Reading Do You Know How to Talk to Aplastic Anemia Experts?
¿Por qué Yoga es la mejor terapia para la espondilitis anquilosante
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¿Por qué Yoga es la mejor terapia para la espondilitis anquilosante

  • Post author:Patient Worthy Contributor
  • Post published:October 25, 2016
  • Post category:Ankylosing Spondylitis/Rare Disease

Conocemos la persona "típico" que practical el yoga: blanca, "de la nueva era", delgada, extremidades delgadas y acrobáticas. ¿Mencionamos delgada? Con los años, el yoga se ha convertido en la…

Continue Reading ¿Por qué Yoga es la mejor terapia para la espondilitis anquilosante
EB and the Butterfly Children of America
source: pixabay.com

EB and the Butterfly Children of America

  • Post author:Octavia Walker
  • Post published:October 24, 2016
  • Post category:Epidermolysis Bullosa/Rare Disease

  They are called, "butterfly children." These butterfly children earned their names for their fragile skin---said to be as delicate as the wings of a butterfly. The official name of…

Continue Reading EB and the Butterfly Children of America
How Much Do You Know About Addison’s?
source: pixabay.com

How Much Do You Know About Addison’s?

  • Post author:Erica Zahn
  • Post published:October 24, 2016
  • Post category:Addison's Disease/Rare Disease

Addison's disease is another name for adrenal insufficiency -- meaning the adrenal glands don't produce enough of the hormone cortisol and frequently create insufficient levels of aldosterone. Cortisol is the…

Continue Reading How Much Do You Know About Addison’s?
The Best Ways to Raise TN Awareness
Source: www.pixabay.com

The Best Ways to Raise TN Awareness

  • Post author:EmpatheticBadass
  • Post published:October 24, 2016
  • Post category:Rare Disease/Timely/Trigeminal Neuralgia (Tic Douloureux)

Looking for great ways to raise awareness (and, therefore, money) for trigeminal neuralgia? Light up your teal lights? TEAL lights…. as in the color. ‘Cuz if pink worked wonders for…

Continue Reading The Best Ways to Raise TN Awareness
What New Hope is Coming for Huntington’s Patients?
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What New Hope is Coming for Huntington’s Patients?

  • Post author:Erica Zahn
  • Post published:October 24, 2016
  • Post category:Huntington's disease/Rare Disease

Approximately one in 15,000 people have a defect in their HTT gene and the outcome of that defect is ultimately life-ending. It's called Huntington's disease, or HD, and the average…

Continue Reading What New Hope is Coming for Huntington’s Patients?
Why Walking is the Best PI Fundraiser
Source: Pixabay.com]

Why Walking is the Best PI Fundraiser

  • Post author:Farrah Fontaine
  • Post published:October 24, 2016
  • Post category:Primary Immunodeficiencies/Rare Disease/Timely

Sunday October 2, 2016 was the IDF Walk For Primary Immunodeficiency (PI) in Boston, MA! As a partnership between the Immune Deficiency Foundation (IDF) and Shire Pharmaceuticals, this walk began at Boston…

Continue Reading Why Walking is the Best PI Fundraiser
CRPS/RSD: I’m Sorry I Didn’t Think of That Dad
Source: flickr.com

CRPS/RSD: I’m Sorry I Didn’t Think of That Dad

  • Post author:PW Blogger
  • Post published:October 24, 2016
  • Post category:Complex Regional Pain Syndrome/Rare Disease

From the day my mother introduced us when I was eight, I've believed my step-father was my hero. He is a strong, hardworking, honest man whom I saw as indestructible.…

Continue Reading CRPS/RSD: I’m Sorry I Didn’t Think of That Dad
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