How I feel a lot of days
I was diagnosed with relapsing remissive multiple sclerosis when I was 26 I want to say 2016 I'm 31 now still living with it. I changed the way I eat I changed a lot of things but I still deal with fatigue I used to be a full-blown athlete I can't even run anymore I walk with a cane and I have a rollator. I don't use it all the time but I have it just in case I'm grateful that I can still walk and move on my own. Everyone who has a disability needs a page like this so we can all get it off of our chest and shoulders and let it be known what we go through yes I understand we all go through things but it's another thing behind that. Are you going to allow what you're going through is that going to make you or break you I believe in God too much to allow it to break me don't get me wrong I do feel weak at times because of this illness but I know who God is 🙌 no it's not easy but I take it a day at a time and keep praying throughout my day. And don't get me wrong I do not expect or want anyone to feel sorry for me it's just me expressing myself. I don't take anything for granted or anyone but this is something that I can't shake I have it for the rest of my life I pray that God removes it and takes it away but this is my story 💪🙌 KEEP GOD FIRST LET HIM DIRECT YOU'RE STEPS PRAY MORE & MORE BUT NOT JUST FOR YOURSELF, FOR THE LOST SOULS. WE NEED EACH OTHER♥️
I was diagnosed with primary progressive back in June of this year. I have also changed a little with what I eat. As much as I love my fastfoods it kills me lol. I still eat pizza though. I also was big on junk foods so I also changed the junk foods I eat. As it is said on Dr. Google, sugar makes fatigue worse. So I see the moment I eat something sweet instantly almost now I get sleepy. So I try to keep it at bay. Sorry about the changes to your athletic hobby/career. I used a walker for almost 2 and a half months. By the grace of God and prayers I have been walking a lot better for the past two weeks now. I agree people with disabilities should have group support like this. It's a blessing to be able to communicate with people we can relate to. MS affects each of us differently but we know there's are people who understands us. To think about it I'm not sure if I can run either. I'ma go outside one day and give it a try around the yard. . .
@Sheilra I thank you so much for your comment and I agree with just about everything that you said it's just we have to find a new way to live life with this disease. It hurts me more because I have two daughters they are six years apart but have the same exact birthday and I can't even run after them or you know be more of a father figure towards them don't get me wrong I cook for him and I play with them but I can't do the fatherly things that I want to do and the things that a man should do