Mental health is such a hot topic for people living with chronic illness. Just do a quick google search, and you will see what I mean. It’s one of the first things that came up in my neurology intake appointment after I described my physical symptoms. Because it’s something I struggled with long before my… Continue reading Mental Health and Chronic Illness
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
Traveling. Believe it or not, this was one of my biggest thoughts in the first few months after my MS diagnosis. I know, I know… there are tons of other things I could have, and probably should have, had on my priority list when I was fresh on this chronic illness journey. Being able to… Continue reading Traveling with Chronic Illness
Well hello there…long time, no talk….or type? Not sure how to phrase that, but you get the gist, I’m sure. I’ve taken a long break from this blog, for various reasons, most of which are mundane and not worth mentioning. Some, however, took my full attention, and for good reason. When I last left off… Continue reading Welcome Back
Grieving is a difficult process, no matter what you’ve lost. I’ve posted tips on dealing with grief after losing a loved one before after my grandmother passed away. Today, I’m discussing something a little different – ways to deal when you’re grieving your old life. Although it’s guided my personal perspective, this is not a… Continue reading Grieving Your Old Life
Today, I’m talking about my Disease Modifier – Rebif. An Interferon injection I give myself 3 times a week; if you’ve been here for awhile, you know I’ve been on it for two years now. If anyone’s counting, that adds up to 312 times that I’ve injected in the last couple years. The last time… Continue reading Two Years on Rebif
It has been SO long since I’ve posted anything – and with good reason. My last post dabbled into what we’ve been dealing with this last year or so, after the pandemic turned all of our lives upside down. It’s hard to know what to say when others are going through so much. But a… Continue reading 3 Years with MS
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
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
