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Being an ally to disabled people requires more than good intentions. In this powerful Patient Perspectives article, a member of our chronic illness community shares what true allyship looks like, from listening and advocating to challenging ableism and improving accessibility. Learn how small actions can create a more inclusive and supportive world for people living with disabilities and chronic illness.

Chronic illness doesn't just change your body, it changes your relationships, your routines, and the future you once imagined. In this heartfelt Patient Perspectives article, one patient shares the often-unspoken grief of saying no to activities they love, watching invitations disappear, and navigating the loneliness that can come with living day-to-day. If you've ever mourned the life you thought you would live, you're not alone.

Chronic illness fatigue is more than feeling tired. This powerful patient perspective shares what it’s like to live with the constant, full-body exhaustion that comes with chronic illness, When rest never truly feels restorative and even simple daily tasks require immense effort.

Many people living with POTS are told to “just get more rest,” but for many patients, sleep itself can become part of the struggle. In this Living Radiantly: Patient Perspectives article, we explore the often-overlooked connection between POTS, fatigue, and sleep disturbances and the emotional toll of never truly feeling rested.

Living with POTS in the summer can feel less like “Hot Girl Summer” and more like survival mode. In this Patient Perspectives article, one writer shares the reality of heat intolerance, symptom flares, hydration struggles, and the small strategies that help make difficult days a little more manageable.

Living with neurodivergence and hypermobility can feel like a constant tension between what your mind expects and what your body can handle. In this patient perspective, we explore the reality of navigating daily life, managing flare-ups, and learning to listen to your body in a world that moves faster than you can.

Welcome to our new weekly blog where hear from our patients about living with an autoimmune disease.