seen from United States
seen from Canada
seen from United Kingdom
seen from China
seen from Russia
seen from France
seen from China
seen from Slovakia
seen from Türkiye
seen from United States
seen from Canada
seen from Malaysia
seen from Malaysia
seen from China
seen from China
seen from United States
seen from United States
seen from United States
seen from Sweden
seen from India
sona vs owner
It'd be nice if I'd actually took a photo of myself and my guitar, but I couldn't predict the feature at the time I was home to do that, now I am far away from home to treat my ms*-ass
* multiple sclerosis
Are we look alike?
The last art credit: @elliereina
It's funny how I've started to hate "good" days.
I felt brilliant yesterday so I was out and about for 5 hours. How stupid of me to think I could actually be a normal human for a day and go out shopping for Christmas and baby stuff. I'm paying for it now of course. I hate good days because they give me a false kind of security that punishes me for my trust the next day.
Ever wonder what other people living with MS go through? Meet Jen O., MS LifeLines’ first video blogger. She’s sharing the good, the bad, and the everything in between of her life with MS. Watch the first episode of “LIFE WITH MS: Jen’s Story” now. More episodes coming soon! MS LifeLines Ambassadors like Jen are sponsored by EMD Serono, Inc.
17th April 2017
I met up with my TC last Monday at the pub for a drink. It was odd. I forgot how much we clicked and how easy it is to talk to him, that we have this same sense of humour so all we did was laugh. And yet, I felt nothing. No butterflies, no sweaty palms, no fidgeting, nothing. I realised P ain't shit, sure he's a great guy but I put him on a pedestal and I'm finally over it. I did it, guys. I did what I thought was impossible. I'm over him.
Whining a little bit more, because I hate it all.
So I was finally diagnosed with MS. The only thing left is to start my DMT. My neurologist was supposed to do just one thing: give me a prescription for the medicine so I can buy it (I don't actually pay for it, bc fortunately I'm living in the country with free healthcare, so that's why it's very important for me. The medicine for MS is very expensive). They kinda did it, but they did it wrong — they wrote the medicine name under “recommendations”. And now I’m very nervous about it.
Thank you for all the good luck! IT WORKED! I finally got my diagnosis lol. (I mean, yelling “Yay, I officially have MS” is a bit weird, but now they’re starting me on disease‑modifying treatment for MS, so that’s something!) I’m so happy 🥰 At least there’s some clarity in my life now.
Having a ms it is argue with your family members that I NEED to call an ambulance
Ever just exhaust yourself getting dressed and then remember there was no need?
I wish I had known I would end up with MS so I could have learnt to drive years ago or not chosen to live a half hour walk from the town. Another day stuck in the damn house 😐
