Facebook-f Twitter Instagram Podcast Youtube Tiktok Linkedin-in Pinterest Envelope Share
SHARE YOUR STORY!
  • About
    • Meet Our Contributors
    • Meet Our Partners
    • Meet the Patient Worthy Team
    • Collaborative Content On Patient Worthy
  • Diseases
  • Share Your Story
    • Patient Worthy Content Submission Guidelines
    • Patient Worthy Writing Prompts
    • Submit Your Story
    • Patient Stories
  • Resources
    • Library
    • Events
    • Patient Worthy FAQs
  • Podcast
  • Contact
Menu
  • About
    • Meet Our Contributors
    • Meet Our Partners
    • Meet the Patient Worthy Team
    • Collaborative Content On Patient Worthy
  • Diseases
  • Share Your Story
    • Patient Worthy Content Submission Guidelines
    • Patient Worthy Writing Prompts
    • Submit Your Story
    • Patient Stories
  • Resources
    • Library
    • Events
    • Patient Worthy FAQs
  • Podcast
  • Contact
  • Join PW

Daily Archives: September 26, 2022

  1. Home>
  2. 2022>
  3. September>
  4. 26
Study of the Week: CAR-T Cell Therapy for Autoimmune Diseases?
source: pixabay.com

Study of the Week: CAR-T Cell Therapy for Autoimmune Diseases?

  • Post author:James Moore
  • Post published:September 26, 2022
  • Post category:Lupus

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…

Continue Reading Study of the Week: CAR-T Cell Therapy for Autoimmune Diseases?
Teen with NPC Becomes Prom Queen for her Birthday
source: pixabay.com

Teen with NPC Becomes Prom Queen for her Birthday

  • Post author:Jessica Lynn
  • Post published:September 26, 2022
  • Post category:Niemann-Pick Disease/Niemann-Pick Type C Disease

  It has been four years since Amaria Granger, now age 14, was diagnosed with a rare disease called Niemann-Pick disease type C (NPC). Since being diagnosed with NPC, Amaria…

Continue Reading Teen with NPC Becomes Prom Queen for her Birthday
With Sickle Cell Disease, a 9 to 5 Job is No Longer Routine
source: pixabay.com

With Sickle Cell Disease, a 9 to 5 Job is No Longer Routine

  • Post author:Rose Duesterwald
  • Post published:September 26, 2022
  • Post category:Sickle cell anemia/Sickle Cell Disease

  Wunmi Bakare described her illness to Essence as a continuous tug-of-war. Balancing sickle cell disease with a nine to five job and trying to stay the course. Then there…

Continue Reading With Sickle Cell Disease, a 9 to 5 Job is No Longer Routine
Duke Earns Recognition as Dystonia Center of Excellence
source: pixabay.com

Duke Earns Recognition as Dystonia Center of Excellence

  • Post author:James Moore
  • Post published:September 26, 2022
  • Post category:Dystonia

According to a story from neurology.duke.edu, Duke University has recently been recognized as a Center of Excellence for Dystonia treatment by the Tyler's Hope for a Dystonia Cure Foundation. This…

Continue Reading Duke Earns Recognition as Dystonia Center of Excellence
More Diverse Blood Donors are Needed to Support Patients with Sickle Cell Disease
source: pixabay.com

More Diverse Blood Donors are Needed to Support Patients with Sickle Cell Disease

  • Post author:Jessica Lynn
  • Post published:September 26, 2022
  • Post category:Sickle Cell Disease

  Did you know that September is National Sickle Cell Awareness Month? During this month, various stakeholders come together to share the stories of those affected by sickle cell disease,…

Continue Reading More Diverse Blood Donors are Needed to Support Patients with Sickle Cell Disease

Featured


Picture of Family


Metastatic Breast Cancer: Navigating Grief


Picture of Ralph Family walking


Rethinking What It Means to Live With Acromegaly


Illustration of mentor program members


The Let’s Chat CAR T One-on-One Mentor Program: Speaking with Someone Who Understands What You Are Going Through

SHARE YOUR STORY!
We believe rare disease patients are people, not a diagnosis. Through education, awareness and some humor, we help patients, caregivers and support persons by providing relevant and often inspirational news and stories.
Our goals are to share stories, cultivate strong community, provide the latest medical findings, connect people and pioneer production of patient worthy information. Help us attain these goals by telling us a little bit about yourself!

Let’s Work Together!

Partner With Us
Submit a Story

Keep Up to Date

Subscribe to Our Newsletter
Check Out Rare Events
Get Inspired By Our Memes

Learn More

About Us
Rare Diseases and Conditions
Terms of Use
Privacy Notice
Privacy Policy for CA Residents
EU/UK Privacy Notice
Data Privacy Framework: Consumer Privacy Policy
Consumer Health Data Privacy Policy
Cookie Notice

Facebook-f Twitter Instagram Podcast Youtube Tiktok Linkedin-in Pinterest Envelope

© Copyright 2024 Patient Worthy

Sign Up With a Patient Worthy Account and Share Your Rare Story

- OR -

Sign Up For Our Patient Panel

Make a difference, share your experiences and get paid. Opt-in and join Patient Worthy's panel for paid opportunities such as surveys, market research, patient advisory panels and more.

More Info

We're Happy You're Here!

What best describes you when it comes to rare disease? (check all that apply)

What rare disease(s)/conditions are most important to you?

Visit Home Page or

Thank you for signing up for a Patient Worthy Account!

Have a rare disease story to share? Let us know

Share Story

- OR -

Sign Up For Our Patient Panel

Make a difference, share your experiences and get paid. Opt-in and join Patient Worthy's panel for paid opportunities such as surveys, market research, patient advisory panels and more.

More Info