I guess it’s better late than never. 2018… The only change for me will be that I will progress. I’m a realist, I have to be. I still hope every day. Yet, hope can become very paralyzing. As most people now, I was diagnosed in August 1997. My second opinion specialist said it began in 1986 and that I am primary progressive. In reality I’ve had this my whole life. I was genetically predisposed for it. I can look back and see issues I had from the time I was little and through my teen years into adulthood. It lay dormant for a very long time. I guess when it showed up, it needed to make itself known by literally taking away everything I held/hold dear.
But, seriously, what you gonna do? I literally can’t “do” anything by myself. I try to keep A happy face because nobody wants to hear the truth. And that’s OK, I probably wouldn’t want to hear it either. So really, what are you gonna do when you end up like this. Basically you just have to take it. I cry so much I could end the drought. 😂 No, seriously, I could. LOL You just have to find the humor.
It’s just that some days there is no humor to be found. It’s been four years and three months now that I have been confined to a bed. I get up for doctors appointments and for showers and that’s about it. The pain is so intense that if I sit for too long… I’m better off in bed.
That’s all I have right now. Happy fucking new year! I’ve just got nothing.
Peace ✌️
Wish I could take your pain away, kick it to the curb..it never makes sense, why some people have to endure the pain and others go through life dodging it..always here for you, my friend..I know pain well.
♥️♥️♥️
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Love you my friend.
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