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Be Your Own Advocate

    It’s Here: The Chronic Illness Revolution
    Chronic IllnessMightier TogetherThe Undefeated

    It’s Here: The Chronic Illness Revolution

    by Ariela Paulsen January 27, 2022February 28, 2022
    written by Ariela Paulsen

    As 2022 races out of the gate, I am feeling hopeful.  For many reasons – some of them purposefully self-fabricated as I described on New Year’s – but one reason looms large in my mind: it’s here, the chronic illness revolution.  I feel like my entire life has been building to this moment.  As a child, my mom (a physician) waffled between suggesting that my symptoms were psychosomatic and asserting that what I had was real (and likely genetic), but some disease that had yet to be discovered.

    She was onto something.  In 2017 – the year I was finally diagnosed in my mid-twenties – experts reexamined what they had learned in the past decade about Ehlers-Danlos Syndrome and rewrote the book.  It was no longer considered rare, but rarely diagnosed, and the diagnostic criteria were revamped and broadcast to the medical world.  In the past five years, the number of people I personally know who have finally found answers thanks to newly educated doctors is staggering.  Also around this time was the discovery of Mast Cell Activation Syndrome and its subsequent research efforts, as well as the foundation of Dysautonomia International and the crucial research and awareness we owe this wonderful foundation.  Today, in my thirties, I finally have the answers I needed for so many years.

    Not only are conditions like the trifecta I live with becoming more understood and treated for what they are — rather than dismissed as “just anxiety” — but tick-borne illnesses and other highly stigmatized conditions like Myalgic Encephalomyelitis are getting attention.  Social media has given a platform for those of us too sick to be visible.  Disability and illness movements have risen to the front of society’s collective awareness thanks to activists and artists (shoutout to the impact of films like Jennifer Brea’s Unrest and her MEAction movement!).  Organizers are working with legislators to include better care for people with Lyme and diabetes.  On an individual level, patients like me no longer have to feel alone!  We see one another on social media, hear each other’s stories reported in the news.  As the world becomes more virtual-friendly, we can meet one another (and those pipe-dream medical specialists!) without having to travel.

    The final push, it seems, for this momentum-building movement was long Covid.  Millions of people have developed the same symptoms that many of us have been suffering with for years – profound fatigue, malaise, and brain fog.  Some also experience tachycardia, shortness of breath, and other symptoms thought to be caused by POTS, a common (yet typically overlooked and gaslighted) type of dysautonomia.  People with long Covid may have similar experiences to those of us who were already fighting with chronic illness, but they have one distinct difference – they all got sick, millions of them, at the same time, in the same way.  It’s one thing for a rigid medical system to write off the story of someone who developed these symptoms after, say, a difficult divorce.  That could conceivably be a body’s response to too much stress.  But millions of people developing the same specific long-term symptoms immediately after contracting a highly researched virus?  That is too clear to ignore!  The reality of chronic illness triggered by infections, viruses, and traumas is now being looked at more seriously.

    Sure, there are still plenty of skeptics in the medical world who claim long Covid isn’t real, is psychosomatic, or is a form of depression, often using the same logic around antibody testing that complicates the lives of Lyme patients.  But, finally, the research is beginning.  Technology is being created to help those with long Covid (and the rest of us) navigate their symptoms to try to find healing.  It is now becoming widely understood that even young people can be chronically ill, that it’s not their fault, and that exercise isn’t always the answer; in fact, trying to push through can make things far worse, as those of us with post-exertional malaise have been trying to convince the world for years.  And when experts like Dr. Anthony Fauci publicly address this new form of chronic illness – validating its legitimacy and pointing out links to other conditions like POTS and ME – it shifts the nation’s zeitgeist to be more open to our stories.

    This became abundantly clear to me when I began hearing stories of chronic illness in the news.  Big media, like NPR, the NY Times, Washington Post, CNN… were finally telling stories that sounded like mine.

    A few months ago, several people texted me on the same day saying “have you heard this story???”  It was from the Ezra Klein Show but hosted by reporter Ross Douthat and his guest Meghan O’Rourke.  These two well-respected reporters shared their own stories of suffering from tick-borne illnesses.  They talked about what it’s like to fight for a decade to get the medical establishment to take your illness seriously.  They shared their grief at having lost a huge portion of their lives to illness.  And they discussed the implications of long Covid on the chronic illness community.  I laughed, cried, and then promptly listened again just to relive the sensation of feeling so heard.  My abled, healthy friends were hearing this.  Maybe, finally, they were getting it.

    Some of the details and nuances discussed in the story hit home because they could only be told by someone who has truly been there.  Details like what it’s like to wake up each day not knowing what face your illness will wear.  In her book, Meghan uses the analogy that if she, say, had a leg amputated, at least she’d know every day that she had to adjust her day for just one leg.  She could gain resources, tools, and workarounds for all that comes with having one leg.  But with some chronic illness, it can change so drastically that you have to constantly rewrite the book.  This not only requires coming up with new solutions but also asking those around you to understand and accept each new form the beast has taken.  

    They discussed the blind spots in our medical system and why it is such a challenge to find care when your illness doesn’t follow the simplistic order of operations taught in medical school.  I know too well the trauma of gaslighting and skepticism from doctors.  Even the wonderful, well-intentioned doctors I’ve met struggle to diagnose and care for those of us with these complex under-researched illnesses. I loved Meghan and Ross’s approach to addressing doctors.  They do not place blame or resentment on doctors, but rather analyze where in the systems we’ve gone wrong.  We have no protocols in place for diseases that look so totally different person-to-person or day-to-day.  We don’t know how to treat when each patient’s version of chronic Lyme or ME responds wildly differently to each treatment.  We don’t have a system set up for the individualized care needed to move forward.

    So, what do we do?  With these stories, the research, and the awareness that has come in the last year, I am more hopeful than ever that we will figure this out.  We must, if not for those of us lost in shadows for decades, then for the millions of new long-haulers out there who are teetering on the brink.

    I hope you’ll join us, this year, in supporting research efforts, sharing one another’s stories, starting conversations, and sending Mighty Well wishes out there into the universe to get this ball rolling!

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  • Emily’s Care Team Tips

    by Ariela Paulsen November 24, 2021November 24, 2021

    As we explored building up a care team last month, we chatted with Co-Founder Emily Levy.  She has recently made…

    1 FacebookTwitterPinterestEmail
  • 5 Tips for Building Your Care Team

    by Ariela Paulsen October 20, 2021April 25, 2022

    Learning to thrive with a chronic illness is a team effort. It’s not something you can simply do through your…

    1 FacebookTwitterPinterestEmail
  • Preparing for the Unexpected

    by Ariela Paulsen October 6, 2021October 6, 2021

    Getting organized for daily life can be a challenge.  Being prepared for potential unexpected detours — like a trip to…

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  • 4 Tips for Advocating to Employers Post-COVID

    by Ariela Paulsen September 20, 2021September 20, 2021

    The struggle to find work that accommodates chronic illness and disability is not new.  Many of us exist in a…

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  • Sick at School

    by Ariela Paulsen September 2, 2021February 23, 2022

    Most kids stay home from school when they feel sick.  It’s comforting to not have to be around others, to…

    1 FacebookTwitterPinterestEmail
  • Lessons Learned on the Road to Acceptance

    by Emmy MacMannis August 3, 2017August 3, 2018

    My name is Emmy, and I’m an 18 year old battling Systemic Arthritis, along with other autoimmune diseases, Mast Cell…

    1 FacebookTwitterPinterestEmail
  • Finding Purpose Through Pain

    by Diana Donnarumma July 27, 2017September 12, 2018

    Founder of Chronically Fit Backpacks, Diana Donnarumma, began creating customized medical backpacks in 2016, inspired by her own personal battle…

    1 FacebookTwitterPinterestEmail
  • President Trump’s 2018 Budget: What’s Getting Cut in the Health Department?

    by Jess Filippone June 13, 2017July 11, 2018

    On May 23, the Trump administration released his full 2018 budget proposal, which details many of the changes that may…

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  • Being Ill in Any Way Is Better When You Are Not Alone

    by Jess Filippone June 8, 2017August 3, 2018

    Jess shares how her “face-to-face” battle with mental illness has made her a stronger person. A few years ago, Jess…

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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.

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Recent Posts

  • 3 Tactics For Managing Anxiety Attacks
  • Top 3 Digital Medication Organizers
  • 7 Things I Wish I’d Known About Motherhood With Chronic Illness
  • Self Care Case: What do you carry?
  • 5 Tips for Navigating Chronic Illness With Executive Function Challenges

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  • Lindy B. on 3 Tips for Coping With Cognitive Dysfunction
  • Ariela Paulsen on 5 Things About COVID Anxiety That Patients Wish Friends, Family, and Colleagues Understood
  • A Glenn JOHNSON on 5 Things About COVID Anxiety That Patients Wish Friends, Family, and Colleagues Understood
  • Ariela Paulsen on It’s Here: The Chronic Illness Revolution

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One positive that came out of the pandemic was tha One positive that came out of the pandemic was that many of us were able to have flexible working arrangements. As more states lift restrictions, heading back to work after months of working from home can be a huge adjustment for so many of us. Allowing time in our schedules for commuting, brushing up on our social skills, and making sure to have access to our medical supplies are just a few things we need to prepare for.

📸 Mighty Well ambassador @ameliablackwater headed back to the classroom last week and is working on finding a happy balance of working, socializing, and finding time for herself. 

If you've returned to work, what was the hardest part about making the transition back? 
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#MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #KeepFighting  #SupportSystem #PICC #PICCLine #Port #Autism #WFH #RemoteWork #Telecommute #MightyWellMask #Pandemic
Before you move forward always be sure to check th Before you move forward always be sure to check the price tag 💵
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#MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #KeepFighting  #SupportSystem #PICC #PICCLine #Port #MentalHealth #MentalHealthAwareness #Anxiety #Depression #PTSD
Life is full of uncertainties. But there will alwa Life is full of uncertainties. But there will always be a sunrise after every sunset 🌅

"The only certainty in life is uncertainty. I challenge you to embrace it. Even if it's just for a bit" ~@kali_rarerootedwarrior ☺️

Featuring: The Mighty Pack & Undefeated Hat
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 #MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #KeepFighting  #SupportSystem #PICC #PICCLine #Port #Gastroparesis #EDS #MastCellDisease
We really love this message from @lizandmollie. In We really love this message from @lizandmollie. In fact, we couldn't have said it better ourselves 🤗 Chronic illness is filled with ups and downs and everyday will look a little different. Know that you're doing your best even on the days that you are flaring, in pain or fatigued. Remember that we are here to support you on the good days, the bad days and all the ones in between 💚 
. 
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#MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #KeepFighting  #SupportSystem #PICC #PICCLine #Port #ChronicFatigue #MultipleSclerosis #Lupus #SickleCellAnemia #Endometriosis #POTS
Going into a medical procedure is always a little Going into a medical procedure is always a little scary. The best way to minimize fear and anxiety is to go in as prepared as you can! If you are feeling nervous for an upcoming PICC line placement procedure, head to our latest blog (link in bio) for some confidence boosting tips so you can feel ready to go! 

📷 Friend in the Fight @zebrajemma loves her PICCPerfect PICC Line Cover. It keeps her PICC line in place without adhesives and is so comfortable 🤗
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 #MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #KeepFighting  #SupportSystem #PICC #PICCLine #Port #IVIG
You can hardly wait to tell everyone what happened You can hardly wait to tell everyone what happened and  suddenly start talking and realize you don't know where the story is going...has this happened to anyone else lately 🙋‍♂️We've been there! Brain fog, perhaps the most universal aspect of illness, is exhausting. Cognitive disorders can be frustrating but take solace in knowing that you are not alone. We've all experienced that foggy feeling 🌫 and although it's not permanent, it can arrive quickly and definitely overstay its welcome. 

Looking for a little help getting the fog to lift? Our Brain Fog Fix Planner is more than just a reminder system. It includes space to track daily symptoms, hydration, thoughts and moments of gratitude amidst the daily challenges and is brought to you with input from our Friends in the Fight® Click the link in our bio to find out more. 
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 #MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #KeepFighting  #SupportSystem #PICC #PICCLine #Port #BrainFog #ChronicFatigue #CognitiveDisorder
We've got your back! Our Mighty Pack is the first We've got your back! Our Mighty Pack is the first medical backpack designed by patients, for patients. Our backpack is perfect for wheelchair users, as it has multiple strap locations to allow for flexibility. Nobody needs to know that you are carrying or wearing your essential medical devices and supplies. As patients ourselves, this is a product that we wish we’d had! 💪💚 Best of all this can be purchased with most FSAs (Flexible Spending Accounts) and HSAs (Health Savings Accounts) Click on the photo to take a look inside the Mighty Pack. 

📹 We are all smiles over this video of Mighty Well ambassador @rebellious_story & her dog Sherlock 😍
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 #MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #Community #Health #Wellness #ButYouDontLookSick #InvisibleIllness #ChronicPain #ChronicIllness #ChronicIllnessWarrior #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #LivingwithChronicIllness #Crohns #InfusionPump #MedicalBackpack #DiabeticLife #Gastroparesis #EnteralNutrition #Wheelchair #Tubefeeding #MedicalSupplies #TubeFed
The school year is quickly coming to a close and w The school year is quickly coming to a close and we wanted to send a Mighty shout out to all the students who worked so hard this year despite the challenges of COVID 🙌 We know that it was a challenging year with limited in-person learning, social distancing, and the requirement of face masks. We are so proud of all of you and you should be too! 💚

📸 Featuring The Mighty Well Mask
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 #MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #KeepFighting  #SupportSystem #PICC #PICCLine #Port #Pandemic #HomeSchool #Graduation #SocialDistancing
I’m proud to be trans and I’m proud to be disa I’m proud to be trans and I’m proud to be disabled — because you can’t put a boundary on being yourself ~@thedisabledhippie
 
Happy Pride Month to all of our Friends in the Fight in the LBGTQIA+ community 🏳️‍🌈
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#MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #Pride #LBGTQ #Transgender #LoveisLove #NonBinary #BiSexual #GayPride #Instalove
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    7 Things Not To Do With a PICC Line

    October 12, 2017
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    PICC Line Complications: Preventing Common Issues

    June 22, 2018
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    Making a Choice: PICC Line vs. Port

    July 20, 2017
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CHRONIC ILLNESS

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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

  • 3 Tactics For Managing Anxiety Attacks

    May 19, 2022
  • Top 3 Digital Medication Organizers

    May 13, 2022
  • 7 Things I Wish I’d Known About Motherhood With Chronic Illness

    May 5, 2022

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mightywell_

One positive that came out of the pandemic was tha One positive that came out of the pandemic was that many of us were able to have flexible working arrangements. As more states lift restrictions, heading back to work after months of working from home can be a huge adjustment for so many of us. Allowing time in our schedules for commuting, brushing up on our social skills, and making sure to have access to our medical supplies are just a few things we need to prepare for.

📸 Mighty Well ambassador @ameliablackwater headed back to the classroom last week and is working on finding a happy balance of working, socializing, and finding time for herself. 

If you've returned to work, what was the hardest part about making the transition back? 
.
.

#MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #KeepFighting  #SupportSystem #PICC #PICCLine #Port #Autism #WFH #RemoteWork #Telecommute #MightyWellMask #Pandemic
Before you move forward always be sure to check th Before you move forward always be sure to check the price tag 💵
.
.
#MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #KeepFighting  #SupportSystem #PICC #PICCLine #Port #MentalHealth #MentalHealthAwareness #Anxiety #Depression #PTSD
Life is full of uncertainties. But there will alwa Life is full of uncertainties. But there will always be a sunrise after every sunset 🌅

"The only certainty in life is uncertainty. I challenge you to embrace it. Even if it's just for a bit" ~@kali_rarerootedwarrior ☺️

Featuring: The Mighty Pack & Undefeated Hat
.
.
 #MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #KeepFighting  #SupportSystem #PICC #PICCLine #Port #Gastroparesis #EDS #MastCellDisease
We really love this message from @lizandmollie. In We really love this message from @lizandmollie. In fact, we couldn't have said it better ourselves 🤗 Chronic illness is filled with ups and downs and everyday will look a little different. Know that you're doing your best even on the days that you are flaring, in pain or fatigued. Remember that we are here to support you on the good days, the bad days and all the ones in between 💚 
. 
.
#MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #KeepFighting  #SupportSystem #PICC #PICCLine #Port #ChronicFatigue #MultipleSclerosis #Lupus #SickleCellAnemia #Endometriosis #POTS
Going into a medical procedure is always a little Going into a medical procedure is always a little scary. The best way to minimize fear and anxiety is to go in as prepared as you can! If you are feeling nervous for an upcoming PICC line placement procedure, head to our latest blog (link in bio) for some confidence boosting tips so you can feel ready to go! 

📷 Friend in the Fight @zebrajemma loves her PICCPerfect PICC Line Cover. It keeps her PICC line in place without adhesives and is so comfortable 🤗
.
.
 #MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #KeepFighting  #SupportSystem #PICC #PICCLine #Port #IVIG
You can hardly wait to tell everyone what happened You can hardly wait to tell everyone what happened and  suddenly start talking and realize you don't know where the story is going...has this happened to anyone else lately 🙋‍♂️We've been there! Brain fog, perhaps the most universal aspect of illness, is exhausting. Cognitive disorders can be frustrating but take solace in knowing that you are not alone. We've all experienced that foggy feeling 🌫 and although it's not permanent, it can arrive quickly and definitely overstay its welcome. 

Looking for a little help getting the fog to lift? Our Brain Fog Fix Planner is more than just a reminder system. It includes space to track daily symptoms, hydration, thoughts and moments of gratitude amidst the daily challenges and is brought to you with input from our Friends in the Fight® Click the link in our bio to find out more. 
.
.
 #MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #KeepFighting  #SupportSystem #PICC #PICCLine #Port #BrainFog #ChronicFatigue #CognitiveDisorder
We've got your back! Our Mighty Pack is the first We've got your back! Our Mighty Pack is the first medical backpack designed by patients, for patients. Our backpack is perfect for wheelchair users, as it has multiple strap locations to allow for flexibility. Nobody needs to know that you are carrying or wearing your essential medical devices and supplies. As patients ourselves, this is a product that we wish we’d had! 💪💚 Best of all this can be purchased with most FSAs (Flexible Spending Accounts) and HSAs (Health Savings Accounts) Click on the photo to take a look inside the Mighty Pack. 

📹 We are all smiles over this video of Mighty Well ambassador @rebellious_story & her dog Sherlock 😍
.
.
 #MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #Community #Health #Wellness #ButYouDontLookSick #InvisibleIllness #ChronicPain #ChronicIllness #ChronicIllnessWarrior #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #LivingwithChronicIllness #Crohns #InfusionPump #MedicalBackpack #DiabeticLife #Gastroparesis #EnteralNutrition #Wheelchair #Tubefeeding #MedicalSupplies #TubeFed
The school year is quickly coming to a close and w The school year is quickly coming to a close and we wanted to send a Mighty shout out to all the students who worked so hard this year despite the challenges of COVID 🙌 We know that it was a challenging year with limited in-person learning, social distancing, and the requirement of face masks. We are so proud of all of you and you should be too! 💚

📸 Featuring The Mighty Well Mask
.
.
 #MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #KeepFighting  #SupportSystem #PICC #PICCLine #Port #Pandemic #HomeSchool #Graduation #SocialDistancing
I’m proud to be trans and I’m proud to be disa I’m proud to be trans and I’m proud to be disabled — because you can’t put a boundary on being yourself ~@thedisabledhippie
 
Happy Pride Month to all of our Friends in the Fight in the LBGTQIA+ community 🏳️‍🌈
.
.
#MightyWell #YouAreMighty #FriendsInTheFight #LiveMightyWell #Undefeated #InvisibleIllness #AutoimmuneDisease #ChronicPain #ChronicIllness #LymeDisease #LymeWarrior #Spoonie #SpoonieLife #SpoonieCommunity #AdaptiveWear #Pride #LBGTQ #Transgender #LoveisLove #NonBinary #BiSexual #GayPride #Instalove
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