Tag: #mswarrior
MS effecting my speech…
βAnother referral due to my MS!
Its crazy how much of ‘you’ MS affects!
My voice hasn’t sounded the same for around 4 years!
Nothing major, I just constantly sound as though I have a cold!
The most annoying thing now is the amount of times I get asked to repeat myself!
I can’t tell what volume I should be using so can occasionally speak very loud!
The worst is when my voice becomes a whisper and I slurr my words!
All because MS has affected my swallow!
When I used to get asked if my swallow was okay at routine check ups, I always thought the consultant meant ‘do I choke often’
Answer: “occasionally”
I never linked the question to the problems I have with my voice! And yet it makes total sense!
Doh!!! π π
Making a down day happier…
βHaving a pretty shitty day today tbh, so fatigued its unreal! Every day lately seems like I have to push myself harder, just to move my body and that’s without actually thinking about what I want my body to do! That takes even more effort! Long gone are those days that I can do things without thinking!
Right now, MS sucks but guess what, I was looking through my pictures on my phone, to find something that reflects my current mood…
That’s when I saw this photo and everything changed!
This photo was taken last Sunday when I yes me, drove the furthest I have ever driven (90 miles to South Yorkshire) to see my MS sister & the rest of our faaaamily! Of course I had my DebbieRahRah as SatDeb & navigator. What makes me feel more proud, was that I drove without feeling nervous!
This beautiful lady is my Kindred Spirit, she has helped me through my MS more than she’ll take credit for! I only need to see her smiley face and my mood lifts!
Thank you Sarah Hickman for making my day cheerier!
(And I know exactly what she’s saying when she reads this… Either “oh behave” or “stoppppp”)
πππππ


