Yesterday, I posted this on my Instagram. It’s a snip of a post I found on Pinterest. I suffered with weird symptoms for YEARS, and I also happen to suffer from two different autoimmune disorders, so this resonated with me. I have used this technique, years ago, with a provider…
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MS + Marriage
The First Year of Marriage With MS Two days ago was my three year wedding anniversary – so why am I calling this The First Year? Because I got diagnosed with Relapse Remitting Multiple Sclerosis a little over a year ago, so I feel like this is our first full year…
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Almost There
This week did not get off to a pleasant start. Without going into too much detail, let’s just say I was the conductor of the hot mess express and my best friend is the craziest passenger of all. (this week) Every time I get stressed out, I get sick. This…
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We Deserve Better
This time two years ago, disability advocacy would have never crossed my mind. I’ve always been the type to go out of my way to be polite and courteous to others; holding doors open, making sure the lady in the wheelchair can get through, walking delicately around the blind guy…
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Hello ❤
Hey there, 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…
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Giving In
I’ve tried writing this a couple times, but admitting when I’m not living up to my own standards is hard. Right now I’m pondering the decision I’ve made to give up the ccma program I’ve been invested in since February. To be honest, the first couple of weeks should have…
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Rebirth
“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,…
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All These Feelings
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…
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Dealing With an Invisible Illness… When You Aren’t Invisible
The disabled population is the world’s largest minority of which anyone can become a part of at any time. For all of us who woke up one day and discovered we’d switched ships during the night, how true is this? Friday marked the beginning of March, and with it, the…
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Feeling Fulfilled
This week has been a fulfilling, exciting blur. Dr appointments, new job stuff, old job stuff, college classes, vocational program classes, and all the extra stuff life with MS brings filled my week up very quickly. I’m loving the new productivity I’m experiencing. It just feels good to get stuff…