Patient Experiences
Caregiver Experiences
#MyositisLIFE Videos
News and Community
Sign In
Register
Donate

Myositis Empower Walk
Site FAQ’s
Our Sponsors
Writing Guidelines
COVID-19 and Myositis

sections

Dermatomyositis
Necrotizing Myopathy
Inclusion Body Myositis
Polymyositis
Exercise
Mental Health
Getting Started
Privacy
MSU Website
Terms
Get Support!

#MyositisLIFE Compose

FAQNew
Our Sponsors
MSU Website

Get Support
Upcoming Events
Donate

sections

Dermatomyositis
Polymyositis
Inclusion Body Myositis
Mental Health
Myositis Mask Memes
Necrotizing Myopathy
#MyositisLIFE News
Videos

#MyositisLIFE Compose

Donate
Myositis Empower Walk

Patient Experiences
Caregiver Experiences

Home
Travel

Travel

Recent

Most Voted
Most Viewed
Most Discussed
Recent
Featured
Random
Most Shared

The travels and tribulations of going on holiday with chronic illness

653

The travels and tribulations of going on holiday with chronic illness

by Lizzy Finn 4 years ago4 years ago

Username Password

Remember Me

Register

Check out these articles

Thriving with Dermatomyositis

by Angelic Ingram
Learning to live with the ups and downs

by Lizzy Finn
The Healing Power of Creativity

by McKenna Telke

MSU on a mission

Our mission is to improve the lives of and empower those fighting myositis through education, support, awareness, advocacy, and access to research.

Disclaimer

Author’s views and opinions in content and media shared with #MyositisLIFE do not reflect those of MSU, its board members, volunteers, or sponsors.

Recent Posts

Thriving with Dermatomyositis

7 months ago7 months ago
Learning to live with the ups and downs

1 year ago12 months ago
The Healing Power of Creativity

1 year ago1 year ago
Myositis Awareness Month Honesty

1 year ago1 year ago
Navigating ambiguity, building resilience, and celebrating wins: what I have learned after three years with a rare disease

1 year ago1 year ago

Myositis Support and Understanding, patient-centered nonprofit organization

MSU on a mission

Our mission is to improve the lives of and empower ALL impacted by myositis through education, support, awareness, advocacy, and patient-centered research.

Author’s views and opinions do not reflect those of MSU, its board members, volunteers, or sponsors. MSU does not endorse any specific provider, device, facility or treatment.

2023 Top-Rated Nonprofit

Myositis Support And Understanding Association Nonprofit Overview and Reviews on GreatNonprofits

Myositis Support and Understanding is a proud Global Genes Rare Foundation Alliance Member

Myositis Support and Understanding is member of the Community Congress

Donate
Myositis Empower Walk

© 2023 All Rights Reserved

Log in

Log in to your #MyositisLIFE account

Remember me

Forgot password?

Don't have an account?

Sign up

forgot password

No worries. Enter your username or email address, then check your email for instructions.

Back to

Log in

Sign up

Sign up for your free #MyositisLIFE account

I have read and accepted the terms of use and the privacy policy *

Back to

Log in

Choose A Format

Story

Formatted Text with Embeds and Visuals

Video

Youtube and Vimeo Embeds

Meme

Upload your own images to make custom memes

Image

Photo or GIF