Looking for the perfect gift for your chronically ill or disabled loved one? The gift of comfort is always the answer! Here are some suggestions that I’ve put together that I think you’ll love giving that I know they’ll love getting! NUMBER ONE: A READING PILLOW FOR THEIR BED Chronic pain and illness can mean…

When I first got sick, it was just all so vague. I hurt. Everywhere. All the time. My primary doc’s answers for years? Stress. Depression. Being a mom. You know….the usual BS. After years of that, neurological symptoms started, so he finally perked up and listened a little and I had hope! But, then came…

Living with small fiber neuropathy is more than just dealing with burning, tingling, or electric-shock sensations in your feet and hands. It can also bring fatigue, sleep disruption, and challenges in finding physical comfort throughout the day. While there’s no one-size-fits-all solution, sometimes the right products can bring blissful relief.I have put together some things…

If you live with Raynaud’s syndrome, you know how painful and frustrating it can be when your hands, feet, or nose suddenly lose circulation. Cold weather, stress, or even holding a cold drink can trigger an episode, leaving your extremities numb, white, and icy cold. The good news? There are plenty of Raynaud’s-friendly products designed…

Halloween is the perfect time to embrace cozy crafts at home. But if you live with chronic illness, chronic pain, limited mobility, or you’re recovering post-op, traditional holiday activities can sometimes feel overwhelming. That’s where low-energy, sit-down crafts come in—creative projects you can do in your pajamas, propped up with pillows, surrounded by warm blankets,…

🧩 My Cozy hEDS-Friendly Jigsaw Puzzle DaysLiving with hypermobility Ehlers-Danlos Syndrome means my joints are never quite as reliable as I’d like. Add in some of the common co-morbidities — chronic pain, fatigue, mast cell activation, and the occasional POTS flare — and my body often has the final say in how my day will…

Painting by Numbers with POTS: My Cozy Creative Escape Some days, my body just doesn’t cooperate. If you live with dysautonomia or POTS, you probably know what I mean—your brain has a list of things it wants to do, but your body throws up a big “Nope” sign. On those low-energy days, I’ve learned to…

Before I had my cervical fusion surgery, I worried about how to best prepare myself and my home to make recovery as smooth and easy as possible. I wanted to share a list of what I needed and used the most so maybe y’all can find some peace and comfort after your surgery. With a…