MS Giggle Grams

About This Club

MS doesn't come with a handbook. No two days are the same. No two people experience the same symptoms. No two bodies respond to the same medications or treatments the same way. Doctors' appointments are a constant rotation of tests, adjustments, and educated guesses. And through all of it, you are figuring it out — largely on your own, largely as you go. Some of you have been living with symptoms for years before anyone gave them a name. Some of you are still waiting for answers. Some of you cannot imagine finding anything comical inside this disease right now — and that is completely valid and completely understood. And some of you have learned, over time, to look back at certain moments and laugh. Not because it wasn't hard. Because it was, and you made it through anyway, and sometimes the other side of hard is funny. I created MS Giggle Grams for all of you. It is a monthly mini book series — real stories from my own life with MS. The moments I can laugh about now. The ones I laughed about in real time. The ones I called my person about immediately after and we laughed until we couldn't breathe. Every month I share one of those moments with you — because laughter heals the soul, and your soul deserves it. 🌸 Each month your envelope includes: ✔️ A handcrafted mini story booklet ✔️ A journal prompt ✔️ A bookmark ✔️ Stickers ✔️ A postcard ✔️ A watercolor image 🌸 Two subscription options — shipping always included: 📖 Full MS Giggle Grams Experience — $15/month 📖 Mini Book Only — $10/month And here's the part I love most: every subscriber has the opportunity to submit their own Giggle Grams story. If your story is published, that month is on me — completely free. Because this isn't just my story. It's ours.