Ms Life
I don’t usually post personal things like this, but I need to be real for a second.
Living with MS is already a battle most people don’t see. The fatigue. The brain fog. The good days that flip into bad days without warning. The frustration of not feeling like yourself.
Recently, my marriage ended. And part of it was because this disease changed things in ways neither of us fully understood.
MS doesn’t just affect the body. It affects mood, energy, stress tolerance, confidence. It changes dynamics in ways that are hard to explain to someone who doesn’t live inside it.
I’m not posting this for sympathy. I’m posting it because if you’re struggling and feel like MS has cost you relationships, you’re not alone.
I’m still here.
Still fighting.
Still building.
Still choosing growth.
This disease may take things from us.
But it doesn’t get to take who we are.
If you’re walking through loss while fighting MS, I see you.

I’m sorry to hear your marriage ended. That’s never easy for anyone. MS is tough. I hate having to live with it and your right, it’s not just the body it effects, it has knock on effects in so many other aspects of life, even identity.
So what you want to post something about how your life is terrible and falling apart at the same time that all of ours are too man. It's pretty selfish and ignorant