Absolutely irritated šš
I absolutely hate living with an invisible disease!!
With an invisible disease, people don't your ill (disabled), because they can't always see symptoms unless symptoms are present.
Like the other day a lady gets on the bus and says "if people have nothing wrong with them they should give up their seat and I'm just like wow, because I knew who they were referring to. I said you shouldn't judge a book by it's cover and pulled out my medical alert card for my MS. I use an electric mobility scooter too sometimes and I've also heard, it's funny how some people will use a mobility device when they can walk and again I'm like wow!! This disease sucks, but the world sucks more.
DONT JUDGE WHAT YOU DON'T UNDERSTAND šÆ
Living with an invisible disease comes with pain everyday, weather we show it or not. š
It sucks ya but canāt let them get to you and bring you down more. Itās obvious for myself as I canāt walk without a full frame but can only inmagin the thoughts going through minds seeing someone in there 30s with a walker. In the end tho weāre just living our lives. People=shit
@BriannaBurham92ā¦.please conserve yourself and try to minimize your stress you put your body through. Please pay attention to the words you use - āliving with an invisible diseaseā. So, it appears you let others decide how you feel based on their poor comments that donāt recognize your struggles. I am selfish and I wonāt gift to anyone my internal peace because they donāt know my battles I am going through daily. I am, though, not rejecting this āflavorā of the condition, but I am trying my best to cope with it. I actually flipped it on its head and used it as a way to be more grateful for my people and situations I experience. I never knew what MS was before I got dxd, but I also never asked or searched for a sexier or more debilitating illness to show to others that I am sick. I had to swallow that bitter pill like a stoic and made the decision to do my best with what I got. I used to be a professional athlete and after I learned what MS is and how it manifests, I was crushed mentally and it took a long time to make peace with myself. My number 1 question is still āWhy?ā after 20 years of struggle. I will never ask for anyone elseās validation or pity for my condition. Good luck in your struggle and please be a bit more resilient and donāt allow other peopleās comments get to you.