Courage is moving forward even when the path isn’t clear: take that step. 🚶‍♀️ #ChronicIllnessWarrior

Planning ahead reduces stress on busy days. What’s your best planning tip? #InvisibleIllness

Recognizing MG eye symptoms early can guide timely care and improve quality of life: https://bit.ly/4lX4ggJ #MyastheniaGravis

Leave a 💤 in the comments if your new motto is “nap now, adult later.” #Spoonie

Spending time with loved ones nourishes your soul. Who do you lean on for comfort? #RareDisease

Self-care is not selfish: it is necessary for your healing. 🛀 #ChronicIllness

Discover Devi Rose’s story: https://bit.ly/46WO3nl At just 13, she began experiencing the symptoms of myasthenia gravis. By 17, she was bedridden and struggling to breathe. #MyastheniaGravis #MGWarrior #MGStrong #MyastheniaGravisNews #Bionews

Overview of MG infusion centers—what to expect and how they support treatment delivery: https://bit.ly/4lVoesi #MyastheniaGravis

Recognizing emotional triggers helps with management. What triggers do you watch for? #DisabilityAwareness

Leave a 🔄 in the comments if your body needs rebooting… please wait. #ChronicIllnessWarrior

There is beauty in your story: even in the chapters written with pain. 🌸 #InvisibleIllness

Don’t miss this event: https://bit.ly/48vbSny On Oct. 23 at 6 pm EST, we’re hosting our live webinar: Pushing Back at MG: From Getting Informed to Taking Action. #MyastheniaGravis #MGStrong #LifeWithMG #MyastheniaGravisNews #MGWebinar #Bionews

When symptoms change, reevaluate your MG treatment with your healthcare team for better outcomes: https://bit.ly/4mOHCZ9 #MyastheniaGravis

Living with chronic illness isn’t a life half-lived; it’s an opportunity to redefine what it means to be truly alive, resilient, and whole. #Spoonie

Advocating for yourself with healthcare providers is empowering. How do you prepare for medical appointments? #RareDisease

Leave a 🙌 in the comments if flare-ups keep you humble. #ChronicIllness

Chart your course to better health with this MG navigator—manage relapses and personalize your care plan: https://bit.ly/4oWGgwU #MyastheniaGravis

If you are broken, you do not have to stay broken. #DisabilityAwareness

Finding ways to adapt daily tasks can improve comfort and productivity. What’s one helpful adaptation you use? #ChronicIllnessWarrior

If you stumble, make it part of the dance. #InvisibleIllness

Know your workplace rights: https://bit.ly/3W2CzIN Should you share your MG diagnosis at work? This decision can feel complicated, but knowing your rights and options can make the choice clearer. #MyastheniaGravis #ChronicIllnessCommunity #InvisibleIllness #MyastheniaGravisNews #Bionews

Energy management in MG explained with the dinner plate theory to help daily planning: https://bit.ly/4nqTO2n #MyastheniaGravis

Leave a 🎬 in the comments if you’re Oscar-worthy at hiding pain. #Spoonie

Your resilience shines brightest in moments others might overlook: keep shining. ✨ #RareDisease

Leave a 😩 in the comments if your exhaustion is so deep, even your tired is tired. #ChronicIllness

Practical travel tips for those living with Myasthenia Gravis to stay safe and comfortable: https://bit.ly/4oWRzVJ #MyastheniaGravis

Sharing progress, not perfection, leads to lasting growth. What small win are you celebrating right now? #DisabilityAwareness

Compassion and patience for yourself are acts of true bravery: be kind to yourself. 💕 #ChronicIllnessWarrior

Leave a 😵‍💫 in the comments if you can’t keep calm because your symptoms have other plans. #InvisibleIllness

An open letter reflecting on life lessons learned with Myasthenia Gravis diagnosis: https://bit.ly/4oXDUhh #MyastheniaGravis

Advocating for accessibility improves quality of life. What accessibility need is most important to you? #Spoonie

Find moments of peace amidst the chaos: they are essential. 🧘‍♀️ #RareDisease

Leave a 🛌 in the comments if the chronic illness club membership includes surprise naps. #ChronicIllness

Current treatment options and advances for Myasthenia Gravis to improve quality of life: https://bit.ly/46cYdjs #MyastheniaGravis

Restoring balance between mind and body takes time. What practice helps you feel centered? #DisabilityAwareness

Connecting through art, writing, or creativity can be healing. What creative outlet do you enjoy? #ChronicIllnessWarrior

Leave a 😂😭 in the comments if medical humor is the only option sometimes. #InvisibleIllness

The Love You Deserve: https://bit.ly/4mneS8U Living with myasthenia gravis reshapes the way we love, from intimacy and dating to the relationship we have with ourselves. #MyastheniaGravis #ChronicIllnessCommunity #AutoimmuneWarrior #MyastheniaGravisNews #Bionews

Mindfulness and hope: navigating the challenges of living with Myasthenia Gravis: https://bit.ly/3JJyuGx #MyastheniaGravis

Remaining flexible allows you to adapt to changing health. What’s one adjustment you’ve made recently? #Spoonie

Your story is one of hope, courage, and perseverance: keep writing. 🖋 #RareDisease

Leave a 🛌 in the comments if your hiding place is beneath multiple blankets. #ChronicIllness

Preventing caregiver burnout when supporting loved ones with Myasthenia Gravis: https://bit.ly/4mxX77C #MyastheniaGravis

Sharing tips and tricks helps the community. What advice would you give to someone newly diagnosed? #DisabilityAwareness

Using mindfulness techniques supports emotional balance. Have you practiced mindfulness recently? #ChronicIllnessWarrior

Leave a ☕️ in the comments if your symptoms change like moods before coffee. #InvisibleIllness

Explore comprehensive information and support about Myasthenia Gravis on the main website: https://bit.ly/4mZD5Tk #MyastheniaGravis

Educating others helps reduce stigma. What’s one thing you wish more people understood? #Spoonie

Your journey with chronic illness isn’t a burden to bear alone; it’s a canvas to paint your resilience and triumphs upon. #RareDisease

Listening to your body is crucial. What signals do you watch for? #ChronicIllness