Facebook-f Twitter Instagram Podcast Youtube Tiktok Linkedin-in Pinterest Envelope Share
MASH Rec CARD (13)
CLICK HERE TO 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

Usher syndrome type 1F

  1. Home>
  2. Usher syndrome type 1F
Researchers are Trying to Develop Gene Therapy for Usher Syndrome type 1F
qimono / Pixabay

Researchers are Trying to Develop Gene Therapy for Usher Syndrome type 1F

  • Post author:Jessica Lynn
  • Post published:May 9, 2023
  • Post category:usher syndrome/Usher syndrome- type 1F

Usher syndrome is a rare genetic disorder that is characterized by deafness and often paired with retinitis pigmentosa (RP), an inherited disease which causes retinal degeneration and vision loss. There…

Continue Reading Researchers are Trying to Develop Gene Therapy for Usher Syndrome type 1F
Rare Disease Week 2022: Liz’s Story – Usher Syndrome 1F in Brazil
source: pixabay.com

Rare Disease Week 2022: Liz’s Story – Usher Syndrome 1F in Brazil

  • Post author:Patient Worthy Contributor
  • Post published:February 23, 2022
  • Post category:usher syndrome/Usher syndrome- type 1F

Rare Disease Week 2022 Rare Disease Week is the week that leads up to Rare Disease Day, which is recognized on the last day of February. This year, we are…

Continue Reading Rare Disease Week 2022: Liz’s Story – Usher Syndrome 1F in Brazil
Study of the Week: A Possible Treatment for Usher Syndrome Type 1F
source: pixabay.com

Study of the Week: A Possible Treatment for Usher Syndrome Type 1F

  • Post author:James Moore
  • Post published:January 31, 2022
  • Post category:usher syndrome/Usher syndrome- type 1F

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: A Possible Treatment for Usher Syndrome Type 1F
Family Takes Action After Facing Usher Syndrome
Free-Photos / Pixabay

Family Takes Action After Facing Usher Syndrome

  • Post author:James Moore
  • Post published:October 1, 2019
  • Post category:Rare Disease/usher syndrome/Usher syndrome- type 1F

According to a story from newton.wickedlocal.com, the first time that mother Melissa Chaikof realized that something was wrong with her oldest doctor was many years ago. When a nearby door…

Continue Reading Family Takes Action After Facing Usher Syndrome
You Are Not Alone: Empowering the Advanced Kidney Cancer Community
Finding Light Through Story-The Power of Ambassadorship in the Endometrial Cancer Community
*cancer that cannot be removed with surgery or has spread to other parts of the body. GEJ= gastroesophageal junction (where the esophagus joins the stomach)
Read Full Story Here
CLICK HERE TO 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