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Mighty Well

  • Shop
    • Shop All
    • PICC Line Protectors
    • Fluid Motion Backpack
    • Self Care Case
    • FSA/HSA Eligible
    • Mighty Merch
    • Wholesale
    • Sale
  • Learn
    • Explore by Treatment Type
      • PICCs
      • Implanted Ports
      • Feeding Tubes
      • TPN
    • Explore by Condition
      • General Chronic Illness
      • Cancer
    • AVA Partnership
      • Ultimate Guide to PICCs
      • Clinician Resources
  • Join Us
    • Be a Friend in the Fight™
    • Brand Ambassador Program
  • Who We Are
    • Contact Us
    • FAQ
    • Our Mission
    • Team
    • Partnerships
    • Media
    • Reviews and Testimonials
    • Where to Find Us
Author

Katie Lustig

Katie Lustig

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    Friends in the FightLyme Disease

    How The Spoonie Community Taught Me to Love My Life, Myself & My Flaws

    by Katie Lustig June 15, 2017July 11, 2018
    written by Katie Lustig

    Katie shares how the spoonie community has not only given her love and support, but also the courage to open up about her battle with Chronic Neurological Lyme Disease. She encourages all chronic illness fighters to overcome the fear of judgment and reveal their journeys to others. Read her blog below: 

    Continue Reading
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  • I Lost My “Creative”

    by Katie Lustig March 20, 2017July 23, 2018

    When I was diagnosed with chronic neurological Lyme last may, I lost a part of my identity– my creative drive…

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  • Beautiful Disguise

    by Katie Lustig March 15, 2017July 23, 2018

    Those of us with chronic mental or physical illness are constantly living in a world of pretend, well at least…

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About Us

Hi, We're Mighty Well.

At Mighty Well, we understand what it means to live with a disability, chronic condition, and illness. Like our community of Friends in the Fight, we are patients and caregivers -and it is the daily challenges we face together that drive us to create products that solve problems and make life easier, safer, more confident, and dignified. We provide outstanding customer support, peer-to-peer feedback, and on-demand digital learning to ensure our customers can access the best-in-class products, support, and community we wish we’d had.

Be a Friend in the Fight!

Recent Posts

  • IgNS Virtual Patient 360 Meeting: Empowering Patients, Caregivers, and Healthcare Professionals 
  • 10 Tips for Organizing Feeding Tube Supplies At Home
  • Multiple Sclerosis Awareness Month: 5 Facts You Should Know
  • A Helpful Guide to Enteral Feeding Pumps for Tube Feeding
  • TPN vs. PPN: Navigating Parenteral Nutrition  

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Popular Posts

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    7 Things Not To Do With a PICC Line

    October 12, 2017
  • 2

    PICC Line Complications: Preventing Common Issues

    June 22, 2018
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    PICC Line vs. Port: Making The Best Choice For You

    July 20, 2017

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Recent Posts

  • IgNS Virtual Patient 360 Meeting: Empowering Patients, Caregivers, and Healthcare Professionals 

    May 11, 2023
  • 10 Tips for Organizing Feeding Tube Supplies At Home

    March 15, 2023
  • Multiple Sclerosis Awareness Month: 5 Facts You Should Know

    March 9, 2023

Disclaimer

The information in this platform is not medical advice and should not be treated as such. You must not rely on the information in this platform as an alternative to medical advice from your doctor or other professional healthcare provider. If you have any specific questions about any medical matter, you should consult your doctor or other professional healthcare provider. If you think you may be suffering from any medical condition, you should seek immediate medical attention. You should never delay seeking medical advice, disregard medical advice or discontinue medical treatment because of information in this platform.

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