Mighty Well
  • Shop
  • Home
  • Friends in the Fight
    • Friends in the Fight

      We Are Mighty Well

      January 22, 2021January 22, 2021

      Friends in the Fight

      Making the Invisible Visible

      December 16, 2020December 16, 2020

      Friends in the Fight

      Holiday Wishlist

      December 4, 2020December 4, 2020

      Friends in the Fight

      3 Ways to Recognize When Someone Needs Support

      December 1, 2020December 1, 2020

      Friends in the Fight

      5 Ways to Give Support to Someone You…

      November 23, 2020November 23, 2020

  • Chronic Illness
    • Chronic Illness

      We Are Mighty Well

      January 22, 2021January 22, 2021

      Chronic Illness

      When Feeling Better Doesn’t Feel Good

      January 13, 2021January 13, 2021

      Chronic Illness

      POTS and ME Awareness: A Surprising COVID-19 Outcome

      January 6, 2021January 6, 2021

      Chronic Illness

      Decorating Your Mighty Pack

      December 23, 2020December 23, 2020

      Chronic Illness

      Making the Invisible Visible

      December 16, 2020December 16, 2020

  • General Wellness
    • General Wellness

      Looking Towards the New Year With Hope and…

      December 30, 2020December 30, 2020

      General Wellness

      Holiday Recipes

      December 9, 2020December 9, 2020

      General Wellness

      3 Ways to Recognize When Someone Needs Support

      December 1, 2020December 1, 2020

      General Wellness

      How to Safely Celebrate the Holidays

      November 21, 2020

      General Wellness

      Introducing: Limited Edition Mighty Well Masks

      November 18, 2020November 19, 2020

  • Shop
  • Home
  • Friends in the Fight
    • Friends in the Fight

      We Are Mighty Well

      January 22, 2021January 22, 2021

      Friends in the Fight

      Making the Invisible Visible

      December 16, 2020December 16, 2020

      Friends in the Fight

      Holiday Wishlist

      December 4, 2020December 4, 2020

      Friends in the Fight

      3 Ways to Recognize When Someone Needs Support

      December 1, 2020December 1, 2020

      Friends in the Fight

      5 Ways to Give Support to Someone You…

      November 23, 2020November 23, 2020

  • Chronic Illness
    • Chronic Illness

      We Are Mighty Well

      January 22, 2021January 22, 2021

      Chronic Illness

      When Feeling Better Doesn’t Feel Good

      January 13, 2021January 13, 2021

      Chronic Illness

      POTS and ME Awareness: A Surprising COVID-19 Outcome

      January 6, 2021January 6, 2021

      Chronic Illness

      Decorating Your Mighty Pack

      December 23, 2020December 23, 2020

      Chronic Illness

      Making the Invisible Visible

      December 16, 2020December 16, 2020

  • General Wellness
    • General Wellness

      Looking Towards the New Year With Hope and…

      December 30, 2020December 30, 2020

      General Wellness

      Holiday Recipes

      December 9, 2020December 9, 2020

      General Wellness

      3 Ways to Recognize When Someone Needs Support

      December 1, 2020December 1, 2020

      General Wellness

      How to Safely Celebrate the Holidays

      November 21, 2020

      General Wellness

      Introducing: Limited Edition Mighty Well Masks

      November 18, 2020November 19, 2020

Mighty Well

Adaptive WearChronic IllnessFriends in the Fight

Adaptive Fashion, Entrepreneurship, and Chronic Illness: Conversations with Keisha Greaves

by Allie Cashel November 22, 2019November 25, 2019
written by Allie Cashel
Adaptive Fashion, Entrepreneurship, and Chronic Illness: Conversations with Keisha Greaves

This month as part of our Friends in the Fight interview series, Emily sat down with Keisha Graves, founder of Girls Chronically Rock.

Keisha lives with Limb-Girdle Muscular Dystrophy and, like Emily, she found her inspiration for Girls Chronically Rock while pursuing her masters degree and knows what is is like to be a young, female entrepreneur living with a chronic illness. She is also a motivational speaker and the Massachusetts State Ambassador for the Muscular Dystrophy Association (MDA).

Keisha shared her story with Emily and spoke about their shared experience as young entrepreneurs, managing both their businesses AND chronic illnesses! Check out their full conversation below.

Thank you Keisha for sharing your story!

Do you have a story to share? Join our Friends in the Fight facebook group to share your story and inspire and motivate others to turn their sickness into strength.

0
FacebookTwitterPinterestEmail
Allie Cashel

previous post
Understanding Physicians’ Perspectives
next post
Gratitude for Those Who Lift Us Up

You may also like

A Fighter’s Journey: Living With a Rare Illness

December 1, 2016

Four ways to use cover wear this summer

May 27, 2019

Cancer Gift Guide: The Best Gifts for Cancer...

April 22, 2019

Holiday Recipes

December 9, 2020

Your First PICC Line – What to Expect

January 21, 2020

Spoonie Stories: Living with Gastroparesis & Feeding Tubes

October 6, 2016

Finding Gratitude Amongst the Madness of Cystic Fibrosis

July 25, 2017

The Biggest Lessons Bipolar Disorder Has Taught Me

March 8, 2017

Gratitude for Those Who Lift Us Up

November 27, 2019

Guide to Difficult Conversations

January 29, 2020

Leave a Comment Cancel Reply

Save my name, email, and website in this browser for the next time I comment.

About Us

Hi, We're Mighty Well.

The mission of Mighty Well is to help patients and their caregivers turn sickness into strength. We are leading the global charge that changes the perception of patients from victims to fighters. We do this by improving the experience of being a patient. We create the products we wish we’d had: functional and stylish apparel and accessories that you can wear with confidence - and content that can help you get through the good times and the bad. It’s wellness you can wear.

Keep in touch

Facebook Twitter Instagram

Instagram

No images found!
Try some other hashtag or username

Recent Posts

  • We Are Mighty Well

    January 22, 2021
  • When Feeling Better Doesn’t Feel Good

    January 13, 2021
  • POTS and ME Awareness: A Surprising COVID-19 Outcome

    January 6, 2021
  • Looking Towards the New Year With Hope and Self Love

    December 30, 2020
  • Decorating Your Mighty Pack

    December 23, 2020

Categories

  • Adaptive Wear
  • Chronic Illness
  • Featured
  • Friends in the Fight
  • General Wellness
  • Healthy Work Environments
  • Lyme Disease
  • Medical Devices
  • Mightier Together
  • Mighty Models
  • PICC Line
  • Popular Posts
  • The Undefeated
  • Treatment and Care
  • Uncategorized

Tags Cloud

Active Lifestyle Adulting Best Fit for Your Lifestyle Be Your Own Advocate blm Chronic Illness coronavirus coronoavirus covid-19 Disabilities Dysautonomia Family Feeding Tubes Fibromyalgia Gastroparesis holidays invisible illnesses Living Mighty Well Living With a PICC Living with a Port LLMD lyme disease Lyme Into Lemonaid Lyme Literate Doctors mental health Mental Illness mighty mask Mighty Pack mighty well mask Misdiagnosed Mom with Lyme New Years Organization Tips PICC PICC line cover PICC Line Dressing Change PICCPerfect PICC Placement POTS Prevention Self-love Support Systems TPN trans black lives matter Working With a PICC Line

Our Story

Mighty Well - Founder - Emily Levy - Our Story

 

It all started with a cut off sock, a cute hockey player, and an 8 AM finance class. Oh, and a PICC Line. That moment inspired us to launch our first product, the PICCPerfect PICC Line Cover.

 

We know it stinks to feel defined by a diagnosis or feel like just a name on a doctor’s chart. Sounds like you? Read how our founder turned sickness into strength.

Recent Posts

  • We Are Mighty Well

    January 22, 2021
  • When Feeling Better Doesn’t Feel Good

    January 13, 2021
  • POTS and ME Awareness: A Surprising COVID-19 Outcome

    January 6, 2021

Join the Fight

Mighty Well's Facebook Page

Find Us on Instagram

No images found!
Try some other hashtag or username
  • Facebook
  • Twitter
  • Instagram

Mighty Well © 2018 All Rights Reserved


Back To Top