kalevine_

kalevine_ Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from kalevine_, Digital creator, Toronto, ON.
(4)

former nurse turned patient advocate 🤍
the girl with the cane + knee scooter ♿️
beauty, real routines & disability tea ✨
as seen in People Magazine
📍Toronto 🇨🇦
https://linktr.ee/kalevine

Three brothers really had me out here pretending I like country 🤠 Jonas Brothers
08/09/2026

Three brothers really had me out here pretending I like country 🤠 Jonas Brothers

08/09/2026

Daddy’s home J O E J O N A S Jonas Brothers Boots and Hearts Music Festival

08/06/2026

Taking a chance because you never know unless you ask 🥹

Last year, Nick proposed the day before we saw the Jonas Brothers, so that concert became part of one of the most special weekends of our lives. Tomorrow, almost exactly one year later, we’re going to Boots and Hearts just to see them again.

Boots and Hearts Music Festival , could you help us complete this full-circle moment and maybe even give us the chance to say hello to the Jonas Brothers? ❤️

Tag Boots and Hearts so they see this🥹🫶

07/19/2026

A little life update: today was the day I had my DRG stimulator trial leads removed.

I haven’t shared much about the process yet because I wanted time to experience it fully and understand how I felt before talking about it online. But I filmed everything, from the procedure and recovery to the different programs, the highs, the challenges, and whether the trial actually helped my pain.

Over the next little while, I’ll be sharing the full journey and answering as many questions as I can about what a DRG stimulator trial is really like.

This has been a lot to process, but I’m ready to bring you along. 🤍

07/05/2026

Long time no post 🥲I explain more in the video, but I’ve had a lot going on behind the scenes and I finally made the decision to move forward with the DRG stimulator surgery next week.

I’m scared, hopeful, emotional, and honestly still processing it all… but I wanted to share this update with you. Thank you for being here 🤍

06/15/2026

I became a disabled nurse at 22, and these are the products that quietly make my everyday life easier.

Some help me feel more independent, some help me save energy, and some help me feel more like myself in a body that doesn’t always cooperate.

06/03/2026

I went into surgery thinking it was the answer.

I thought I’d have the neuroma removed, heal for six weeks, and finally get my life back.

But what happened after was something I didn’t even know was possible and it changed the entire direction of my life.

This is why informed consent matters. This is why patient education matters. And this is why I’ll never stop talking about what it feels like to be on the other side of healthcare.

Episode 1 of Things Never Break is out now. Link in bio 🤍

I had no idea there was even going to be a second article 😭I opened Facebook and saw that had published another piece a...
06/01/2026

I had no idea there was even going to be a second article 😭

I opened Facebook and saw that had published another piece about my story, this time about what becoming disabled taught me about medical dismissal, patient advocacy, and how vulnerable it feels to be on the other side of healthcare.

This part of the story matters so much to me because I know how many people are quietly fighting to be believed.

For every patient who has ever left an appointment feeling dismissed, unheard, or like they were falling through the cracks, this conversation is for you. 🤍

Have you ever felt dismissed by the healthcare system?

Link is in my bio🤍

05/31/2026

published my story. About CRPS. About chronic pain. About what it actually looks like to lose your health at 22 and have to rebuild everything.

For so long this condition felt invisible. Dismissed in waiting rooms, told it wasn’t that bad, fighting to be believed by the people who were supposed to help.

This is what happens when we keep talking anyway.

I’m so proud of this community. You showed up, you shared your stories, and now the conversation is bigger than any of us. People are finally recognizing what chronic pain does to a life, and that matters more than I can put into words.

Link in bio. Read it, share it, send it to someone who needs to feel seen today. 🤍

If the PEOPLE article brought you here, I’m so glad you found this page. 🤍There is so much of this story that could neve...
05/28/2026

If the PEOPLE article brought you here, I’m so glad you found this page. 🤍

There is so much of this story that could never fit into one article, one caption, or one 60-second video.

So I built a place for the rest of it.

kalevine.com is where I’m sharing my story, longer journal posts, resources I wish someone had sent me sooner, and digital tools made for people who want to feel more prepared, less dismissed, and less alone in appointments.

And Things Never Break is the podcast where I talk about the parts of chronic pain, disability, grief, medical trauma, and identity loss that people don’t always know how to say out loud.

This all started from a life I never expected to be living.

But if sharing it helps even one person feel seen, believed, or a little less alone, then it matters.

Thank you for being here. The article, website, and podcast are all linked in my bio. 🤍

Address

Toronto, ON

Website

Alerts

Be the first to know and let us send you an email when kalevine_ posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Shortcuts

Share

Category