I’m Setting New Year’s Goals, Not Making Resolutions
How do you feel at the start of a new year? I love it, because I enjoy defining my intentions…
Jessie is the host of the DISabled to ENabled podcast and author of the "ENabled Warriors Symptom Tracker" book. She's also an illustrator working with MS charities and magazines worldwide. She’s interviewed paralympians, radio DJs, chronic illness bloggers, marathon runners, and more. Jessie, based in the U.K., was diagnosed with MS at 22 years old and was told by a doctor to "go home and Google it" to find out what MS was for herself. Her own experience of being newly diagnosed so young was negative and scary, so she fills the internet with positivity for other anxious MS Googlers to stumble upon.
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How do you feel at the start of a new year? I love it, because I enjoy defining my intentions…
“She smelled amazing!” I commented to my oblivious husband as we walked our muddy dog back home after…
What would happen if you switched off all of your devices for a day? Phones,…
For many of us, odd symptoms and strange feelings may fill our lives for years before we are…
“I’m too hot!” My brain was turning to mush as my body…
A pet is the most loyal companion a person can have. I’m currently…
The end of the year is incredibly difficult. We already have to put up with more than…
Annually, I’m frustrated by the changing of our clocks due to the end of daylight saving time.
Did you know that there are various types of fatigue, and each makes us feel…
It doesn’t take much for us to feel uncertain. It could be the result of a new symptom or…
Finding an understanding community makes such a difference to people diagnosed with multiple sclerosis (MS). Our…
When I was first diagnosed with MS, I didn’t have a choice about…
A multiple sclerosis diagnosis is hard to process. Our body that we once knew…
“I’m just lazy,” I told myself. “Why can’t I do the things I need to do? I’m so…
Multiple sclerosis is an unpredictable disease that can fluctuate at any time. It’s difficult to predict…
Many people with multiple sclerosis (MS) struggle with intestinal issues. There is…
People outside the U.K. might not understand this column, but that’s OK. Not long ago, we had an entire…
After I received my diagnosis of multiple sclerosis, my nurse handed me…
Your alarm sounds at 7 a.m. You grunt, smash the snooze button, and turn over.
“What was the date of your last relapse?” the neurologist asked while peering over her glasses at me. …
After you get a new diagnosis and are coming to terms with a new way of life, the next…
Rose petal confetti — made from the roses my dad had given me a few days before — rained…
“You look OK to me.” He stood, towering over me, his big belly billowing from his shirt as…
I saw this question asked in a group somewhere not long ago and it got me thinking. …
Note: This column was updated July 23, 2020, to remove erroneous information about red blood cells. We regret the error. …
I’m a fraud. Or at least I feel like one. When writing for a…
Last updated April 25, 2023 In June, the U.K. marks Carers Week, which got me thinking about how…
Who wants to go on holiday?! I know, I know, we can’t physically go anywhere right now, but…
You’re chronically ill, super anxious, crazy shy, unconfident, and have no interviewing skills.
There’s something we need to address, right here, right now. Not all of you will like it or…
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