Tweet Teratas untuk #cpprobs
I may look like I'm reclining at my desk, but I'm really just trying to relieve my hip and back muscles from my circumstances of perpetual sitting. #CPprobs
Stop tagging me on twitter if you want me to write.... #CPprobs
Highlight from today
After mani/pedi
@TiffanyLeaElmer: your nails look like the planet
Me: the one? Just the one planet?
Her: I meant EARTH
In conclusion, Tiffany is a flat earther
Walking a big dog can be problematic at the best of times, and I’m a dog person #CPprobs #CerebralPalsy
For the first time in a long time, maybe ever, I’m prioritizing my long term health instead of working through pain. It’s not necessarily a great feeling, but I’ve realized it’s a priority. #CPprobs #CerebralPalsy
Lifting heavy things has always been an issue, however I’ve perfected the kick or drag the box across the room strategy 😂 #CPprobs #CerebralPalsy
It can be a struggle to find people to talk to who understand the issues and challenges you are facing. Family and friends are great and in my case have been extremely supportive, but there is a difference between sympathy and empathy #CPprobs #CerebralPalsy
Support for young adults w/permanent disabilities, whether they are labeled “high functioning” or not, is so important and it’s not talked about enough. On top of normal stress and issues, they are dealing with a new awareness of their disability. #CPprobs #CerebralPalsy
Someone told me that CP is thought of as a children’s disease, and I realized there’s a lot of truth to that. There are a lot of heartwarming stories about kids, but just because they grow up doesn’t mean their issues go away. If anything they get worse #CPprobs #CerebralPalsy
You become so used to pushing yourself further and harder that when a breaking point comes, whether it be from running too much or working in adverse conditions, it’s hard to force yourself to stop and live to fight another day #CPprobs #CerebralPalsy
Working a labor intensive job #CPprobs
Various questions: “How did you get CP?” “Will it get worse?” “How do you deal with it?”
CP isn’t a disease to fight or something that can be overcome. I was born with it, and it’s the only life I’ve known. I wouldn’t trade my experience for anything. #CPprobs
Anything requiring remotely good balance usually ends poorly for me, like putting boxes on high shelves at work #CPprobs
Understanding there are things I can’t do or would take me a lot longer than the average person, and understanding that asking for help isn’t the same thing as giving up #CPprobs
Some kind of pain. Whether it be ankle, knee, back, or wrist, there is always at least mild pain due to muscle tightness or fatigue (on my affected side) or over exertion (my strong side)
There are ways to treat it, but it never really goes away and that’s my normal
#CPprobs
Me and fireworks are not friends...🙈🙄 Remember to keep your pets and CP’s safe and inside tonight!😂 #BonfireNight #Cpprobs
It's been three months since I left Disney and I'm still struggling to figure out how to take a good selfie with no Mickey Ears 😭 #CPProbs
I walked today for the first time in like years.... damn it felt good. And I hate to admit it but it was even better in my braces. #CpProbs
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