When Numbness Became My Wake-Up Call: My Journey to a CIDP Diagnosis

What started as tingling in my hands slowly turned into a life-changing diagnosis: CIDP. This is my story of pain, patience, and the grace I found along the way — proof that even in the hardest moments, there’s still light in the growing.

The Search for Answers

It started as something small — something I brushed off. A tingle here, a little numbness there. My hands felt like they’d fallen asleep and just hadn’t quite woken up yet. I figured maybe I’d slept funny, or perhaps I’d overdone it the day before. I’m used to pushing through discomfort. Most of us are.

At first, I thought it might be something simple. Vitamin deficiency? Maybe nerve compression? And then one day, I fell and couldn’t get up. An ambulance came and took me to the hospital, and I was admitted. And so began the long, confusing carousel of tests — bloodwork, nerve studies, pokes, prods, and more waiting than I ever thought possible.

Each test felt like a tiny chapter of hope — until another “We’re not sure yet” pushed me back into uncertainty.

If you’ve ever lived in that waiting space, you know how loud it can get inside your head. Every tingle becomes a question. Every unanswered call from the nurse’s office feels like a cliffhanger in a story you didn’t ask to star in.

The Day I Heard “CIDP”

I was initially diagnosed with GBS (Guillian-Barré Syndrome), but soon after, my neurologist finally sat me down and said, “We think it’s CIDP — Chronic Inflammatory Demyelinating Polyneuropathy.” I remember nodding like I understood, but truthfully, I didn’t. It sounded clinical, foreign — too big to fit into the small, quiet life I knew.

Part of me felt relief that it wasn’t “all in my head.” Another part of me grieved the simplicity I’d lost — the days when walking across the room didn’t require courage or calculation.

Learning to Live with It

CIDP changed my life. There’s no sugarcoating that. But it also slowed me down in ways that revealed unexpected grace. I began to notice the small mercies: my husband’s patience when I needed help standing, the way prayer and meditation became less routine and more lifeline.

Most days, I hurt — physically and emotionally. Some mornings, my body feels like it’s made of static. The truth is, living with CIDP means living in the in-between — between pain and peace, frustration and faith, exhaustion and endurance.

Finding Grace in the Growing

If there’s one thing this journey has taught me, it’s that growth rarely comes wrapped in comfort. But even when my nerves misfire and my muscles tremble, grace shows up — sometimes quietly, sometimes through tears, sometimes in the form of a hand I didn’t have to ask for.

I don’t have all the answers, but I have a story. And if my story helps someone else feel seen — even for a moment — then maybe that’s what all this is for.

Today Has Been An Okay Day

Today has been an okay day. I’m taking a course to help build my blog so that has kept me busy.

Today has been an okay day. I’m still in quite a bit of pain. Typing this is hard because my hands and fingers are numb.

I’ve been taking a Skillshare class on organizing tasks for launching a course, but I’m applying it to my blog. I’m learning a lot and am looking forward to applying what I’ve learned. I really want to make this something that will share my health experience, but also I hope to help other people experiencing the same thing. I know I’ve already written about that.

I have been pretty unproductive today, except for researching blog stuff. I slept late, as usual. This disease is so baffling. I try to move about my day, but I am not that successful. John is doing everything to run our life — laundry, dishes, cats, etc. I am very thankful for him, but struggle with feeling so guilty that he is doing everything. Truth be told, I can’t really do much of anything. I can barely get myself to the bathroom and back. It is incredibly frustrating for me, but I try to give myself grace. I’m hopeful that this will not last forever, and I can get back to my life and routines.