How has it already been five years? I remember half walking, half dragging the numb side of my body into the hospital in 2018. The day before my husband’s 30th birthday, incidentally. After a month of dealing with steadily worsening numbness, fatigue, and pain, amongst many other troubling symptoms. I knew what was going on,… Continue reading 5 Years with Multiple Sclerosis
The last month has really flown by for me – how is it already October?! Where did the time go? Oh yeah, it all went to recovering from pneumonia, getting through school, and starting back at work. I’m not complaining; I’m just exhausted. I posted a couple weeks ago about Managing Chronic Illness and College,… Continue reading Medical PTSD
So in my last post in this series, I went over what exactly MS is. In this installment, I’ll be going over some of the different types of MS. MS has four generally recognized courses. There are a few rarer types I’m not covering here in depth. I may be able to cover those later… Continue reading The Different Types of MS
The past couple of weeks have flown by around here. We attended a class called Relationship Matters, put on by the National MS Society. Its focus is on serious relationships with ms as a third wheel, and we definitely fall into that category. The facilitators of the class were excellent, and I can really say… Continue reading Feelings Check In
This month marks one full year that I’ve been on Plegridy. It’s an Interferon beta-1a used to treat Relapse Remitting Multiple Sclerosis. I inject it subcutaneously every 14 days. The last year has gone by quickly, but I’ll never forget it. When I first started Plegridy, I was just chomping at the bit to get… Continue reading One Year on Plegridy
Full disclosure – this is a revamped version of my very first post. I took it down for a while, for various reasons. I was unsure of the purpose, I was freshly diagnosed and confused, and mostly I was very self-conscious. I’ve edited a few parts with more clarity now that I have another year… Continue reading Diagnosis Time – Revisited
Hey everyone! I’m Bri I started Stumble Pup when I was freshly diagnosed with Relapsing Remitting Multiple Sclerosis. I’d been struggling with mysterious symptoms for years, and had several different misdiagnosis. Once I finally heard those words, I made a promise to myself – I promised I was going to take my life back, and… Continue reading Hello ❤
The 2019 Indianapolis Walk MS Event was huge. I don’t mean just space wise, although they took up quite a bit of White River Park. I mean the mood was huge. I woke up feeling flarey – I know, bummer, after feeling so good the past couple of days – but got on the road… Continue reading Walk MS Indianapolis 2019
“Nothing in the world is worth having or worth doing unless it means effort, pain, difficulty… I have never in my life envied a human being who led an easy life. I have envied a great many people who led difficult lives and led them well.” Theodore Roosevelt April 8th, 2018, was one hell of… Continue reading Rebirth
If you follow me on Instagram, you know I’ve had a lot going on, but didn’t want this week to pass before I brought up a couple of things. First up are the ignorant comments from Dr. Phil. He had the audacity to say 100 out of 100 care giving relationships fail. Really. I’ll only… Continue reading All These Feelings
