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

432 Search Results Found

You searched for: "parkinson's"
  1. Home>
  2. Search results for “parkinson's”>
  3. Page 44
30 Million Euros Allocated to Fund Precision Medicine Research Projects for Neurodegenerative Diseases

30 Million Euros Allocated to Fund Precision Medicine Research Projects for Neurodegenerative Diseases

Precision mNedicine is the latest craze in rare disease research. Thankfully for patients, it is completely, 100% centered on improving the quality of their care. Unlike most typical healthcare practices,…

Continue Reading 30 Million Euros Allocated to Fund Precision Medicine Research Projects for Neurodegenerative Diseases
National Geographic Features Innovative Research That Will Advance Precision Medicine

National Geographic Features Innovative Research That Will Advance Precision Medicine

Perhaps the most difficult thing about rare disease research is that not only do the conditions affect only a small portion of the population, but like every diagnosis, they affect…

Continue Reading National Geographic Features Innovative Research That Will Advance Precision Medicine
Patient Centricity Helps Facilitate The Introduction of New Therapies for Rare Diseases

Patient Centricity Helps Facilitate The Introduction of New Therapies for Rare Diseases

According to a story from Pharmaphorum, there are a number of new treatments that have been introduced or have seen major strides in development over the last year. More patient…

Continue Reading Patient Centricity Helps Facilitate The Introduction of New Therapies for Rare Diseases
CZI has Committed 64 Million Dollars to the Research of Neurodegenerative Disorders

CZI has Committed 64 Million Dollars to the Research of Neurodegenerative Disorders

Neurodegenerative disorders affect millions of people across the world. They include Amyotrophic Lateral Sclerosis, Parkinson's disease, Huntington's disease, and Alzheimer's disease, among others. For most neurodegenerative diagnoses, there are no effective treatments, no…

Continue Reading CZI has Committed 64 Million Dollars to the Research of Neurodegenerative Disorders
Motor Neuron Disease Research Drive Underway with £50,000 Donation

Motor Neuron Disease Research Drive Underway with £50,000 Donation

According to an article from The Herald, Scottish Rugby legend Doddie Weir's My Name'5 Doddie Foundation has contributed £50,000 towards pre-clinical development of a drug to treat motor neuron disease.…

Continue Reading Motor Neuron Disease Research Drive Underway with £50,000 Donation
Remembering President George Bush and His Links to the Rare Disease Community 

Remembering President George Bush and His Links to the Rare Disease Community 

President Herbert Walker Bush passed away on Friday, November 30th at the age of 94. News coverage of his life has reminded us all of the great legacy he leaves…

Continue Reading Remembering President George Bush and His Links to the Rare Disease Community 
Paris Parents Start “Kisses for Leo” Campaign for son With Rare Infantile Neuroaxonal Dystrophy

Paris Parents Start “Kisses for Leo” Campaign for son With Rare Infantile Neuroaxonal Dystrophy

  When Deborah, a New Yorker, flew over to Paris to do an internship for an architecture office, she never knew she would be flying across the world and meeting…

Continue Reading Paris Parents Start “Kisses for Leo” Campaign for son With Rare Infantile Neuroaxonal Dystrophy
Vote to Help Family Win 50,000 Dollars for Mitochondrial Disease Research!

Vote to Help Family Win 50,000 Dollars for Mitochondrial Disease Research!

There are only 11 people in the world diagnosed with Mitochondrial Complex 1 Deficiency. Katherine Faughn, a 7-year-old living in Kentucky is one of these 11. The disease wasn't even…

Continue Reading Vote to Help Family Win 50,000 Dollars for Mitochondrial Disease Research!
  • Go to the previous page
  • 1
  • …
  • 41
  • 42
  • 43
  • 44
  • 45
  • 46
  • 47
  • …
  • 54
  • Go to the next page

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

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