So I’ve had this odd habit of popping my hip in and out since I was a kid…anytime I was standing still, I could feel this little bone popping in and out of place when I moved just right. Little did I know, this quirky subluxation would end up helping my doctors finally diagnose my… Continue reading What is EDS?
I wish I had some upbeat, informational post to share with you today. I wanted to do a post on EDS, ableism in the chronic illness community, and others this month…I still hope to get another one out, but, we’ll see. So why am I here? Just to say – I see you. You, with… Continue reading Hang In There
I wasn’t expecting health issues other than MS to take a front seat so soon, but here we are. Today, I’m going over all my best tips + tricks for dealing a back injury and the pain that accompanies it. In my case, a slipped disc is the culprit. It started about three weeks ago,… Continue reading Dealing With a Back Injury
The summer is absolutely flying by, like the rest of the year has. Since March, I’ve found myself in a lot of different places I never expected to be. I definitely never thought I’d be living through a pandemic, or potentially the biggest civil rights movement America has ever seen. Yet, here we are. For… Continue reading Silence is Complicity – Resources for White Allies
Another year has come and gone – but this one looks a lot different than last, does it not? This post is a little late, as this anniversary came + went last month. Of course, more time just gives us more perspective. (that’s my excuse and I’m sticking with it.) Like I expect most who… Continue reading 2 Years with MS & 11 Months on Rebif – A Quick Update
This will be the first of a few posts this month. I’ve finally finished up a hectic semester amidst new, distracting circumstances. I wasn’t planning on doing a post dedicated entirely to the COVID-19 pandemic; I think you probably see quite enough of it in your news feed as it already is. However, as time… Continue reading A Calm Quarantine – COVID 19 Isolation Ideas
Like a lot of the rest of the world right now, I’m practicing social distancing. Being stuck in the house is nothing new for me, or a lot of the chronic illness community. Feeling well and isolating is new for me, though. As such, I’m finding new things to keep me occupied, and decided one… Continue reading Creating a Medical Binder
If you don’t have MS, or are newly diagnosed, you may be thinking – what in the world is a disease modifying drug? They’re also known as DMT’s, or disease modifying therapies. In the past, these drugs were used only for RRMS to help modify disease activity. Specifically, DMD’s have been found to – Reduce… Continue reading Disease Modifying Drugs and MS
As I’m a little yeah I won’t pretend, I’m completely obsessed with my pets – I thought I’d spruce up another post from the past. Life with fur babies when you’re disabled is half hot mess and half unconditional love. Everyone who knows me knows I’m in love with my little zoo, and are definitely… Continue reading Life As A Disabled Fur Baby Mama
Since I started the Fall semester last year, you may have noticed a decline in the amount I’m posting here on StumblePup – you would have noticed correctly if so. I’m not going to even try to front; I have been absolutely, positively slammed since I started school started up last August. Not to mention,… Continue reading Midwinter Update
