Tell one person about MG

dedicated to raising awareness of Myasthenia Gravis.

My wish is that, at least once in this month, each one of us will tell someone else about, introduce them to:

Myasthenia Gravis
a rare, chronic, autoimmune
neuromuscular disorder for which there is no cure

Today, learn one more thing…how to pronounce the words:
my-us-THEE-nee-uh GRAV-is, (GRAY-vis)
myasthenia gravis.

Become part of the ‘ripples of hope’

When you skip a pebble across still waters, you create ripples. The molecules begin to come alive. They begin to nudge one another, begin to affect one another, and pretty soon they are dancing together in waves, splashing across the waterways.

Awareness is like that. When we tell someone about myasthenia gravis, one person tells one person who tells one person and pretty soon many people have felt ‘the ripple’ through conversation. MG will no longer be a secret; people will become aware.

Tell one person, start a ripple. Your words will expand and an awakening will begin…those ripples will become waves of knowledge and an ‘aha’ moment for someone.

That’s what awareness can do!

I DID IT!

Let’s celebrate the advancing ripples together! Now, that you have learned the name, how to pronounce it and what it is, basically, and have told one person…please, go to the bottom of the page and write, ” I DID IT! I told one person.”

Easy, peezy

  1. Learn something about myasthenia gravis.
  2. See What is Myasthenia Gravis? to add to your understanding.
  3. See Resources for MG if you yearn to learn for more.
  4. Tell another person about myasthenia gravis.
  5. After that, go to the bottom of the INSPIRATION page on this site and make some excitement….write:
    “I DID IT” in the comments.
  6. You rock! You are awesome!!
    You can make a difference. Thank you!!!

Next post, June 7 “What is Myasthenia Gravis?” by Rebekah Dorr from Myasthenia Gravis Unmasked group on Facebook.

Watch our right side bar during June Awareness Month as throughout the month we add posts about many aspects of Myasthenia Gravis.

Thank you…you’ve made my heart sing!

Please, SHARE THIS SITE ...
others can learn by reading what you have discovered… a site solely for awareness of Myasthenia Gravis.


Art credit, iris garden: Nicolai Mitrushov on etsy
Iris = Wisdom and HOPE

Twenty-seven days to tell one person (c) 2021 Judith Allen Shone

Thirty days to raise awareness

dedicated to raising awareness of Myasthenia Gravis.

My wish is that, at least once in this month, each one of us will tell someone else about Myasthenia Gravis,

… a rare, chronic, autoimmune
neuromuscular disorder for which there is no cure.

Become part of their hope

Let’s find time to reassure those seeking a diagnosis that we want to be part of their hopeour encouragement takes only as much time as to read this site, while we drink one coffee together!

Our effort to learn so we can introduce MG to someone who never has heard of it, like the ripples in a stream, will begin to reach those who are searching, and will make a huge difference in untold lives.

Watch our right side bar during June Awareness Month as throughout the month we add posts about many aspects of Myasthenia Gravis.

Easy, peezy

  1. Learn something about myasthenia gravis.
  2. See What is Myasthenia Gravis? to add to your understanding.
  3. See Resources for MG if you yearn to learn for more.
  4. Tell another person about myasthenia gravis.
  5. After that, go to the bottom of the INSPIRATION page on this site and make some excitement….write:
    “I DID IT” in the comments.
  6. You rock! You are awesome!!
    You can make a difference. Thank you!!!

Thank you…you’ve made my heart sing!

Please, SHARE THIS SITE ...
others can learn by reading what you have discovered… a site solely for awareness of Myasthenia Gravis.


Art credit, iris garden: Tatiana Mitrushova on etsy
Iris = Wisdom and HOPE

Thirty days to raise awareness (c) 2021 Judith Allen Shone