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
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
If you’ve been reading Stumble Pup for awhile, you know I’m very passionate about mental health awareness. I’ve previously talked about how depression is associated with MS, and covered how I personally deal with it here. I’ve also talked about how therapy helps with my anxiety and dealing with trauma. So why am I bringing… Continue reading Chronic Illness and Therapy
I last checked in when I’d been on Rebif for 9 weeks; it’s been 5 months now. That’s 63 injections, if anyone is counting – oh no, just me? (If I had time to grab my phone to add an eyeroll emoji here, I would.) I’m mostly joking; overall, Rebif is treating me much better… Continue reading 5 Months on Rebif
In my last post, I went over some of the best tips I’ve found for surviving the holiday season when you have a chronic illness. In this post, I’ve come up with something much more fun – a list of the coolest presents I’ve found this year. I also included what my family has started doing… Continue reading 9 Unique Gifts For The Chronically Ill
Now that Halloween has passed, and we’re well into November – I’m beginning to notice around me everything holidays. The store shelves have been wiped of all things spooky; replaced with shimmery tinsel, shiny ornaments, and a couple of tree toppers for good measure. All the trees have changed colors, and they’re beginning to drop… Continue reading Chronic Illness and the Holidays
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
I’m currently in my second year at college, pursuing a degree in Social Work, and eventually hope to get my Masters, too. I’m also a year and a half deep into a Multiple Sclerosis diagnosis. Learning to manage the many hats that come along with those two titles has been a real struggle for me.… Continue reading Managing Chronic Illness and College
