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…
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When Doctors Ignore Your Symptoms
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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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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Because I Missed Friday Feelings
Today, as I was searching through degree maps and generally planning out the next couple of semesters, a thought struck me that hasn’t in a while. Who am I? Not in that spooky existential way – that I don’t have time or brain capacity to discuss in ten lifetimes. Life…
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5 Tips for Dealing with Grief
Recently, I was re-acquainted with a very old friend – grief. He is far from a stranger to me; I’ve lost many people in my short 27 years. Enough that I’ve developed some excellent coping mechanisms. That being said, losing someone never really gets easier. The initial shock doesn’t hit…
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A Kinda Fab Friday
It’s been a really great week around here, despite getting the news about my dumb heart tests + monitor. I get that the tests aren’t necessarily stupid, ok, I just detest having to sport a monitor and carry a phone for a month, not to mention spending my Monday at…
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A Little Bit More
I’m Bri, and I’m thriving with RRMS. Stumble Pup is my way of trying to find my way in the new community I find myself a part of, and to provide a little soft space to land for those struggling with MS or mental health issues. Basics first; I was…