After a few days in the hospital on a daily Solumedrol infusion, I was able to go home. My vision is better but it’s not back to where it was before. Every day I wake up is a blessing, but it’s also a struggle. I’m always in pain, my hands or legs are always tingling. I get sharp pains out of no where, they come and go. My pain levels go from 0-10 all day. It seems the more I learn about this disease, the more questions I have, but I can never really get a real answer. It’s really hard to explain what I go through every day to someone who doesn’t have MS, so I keep it in. I found out it’s better to talk about it, which is why I decided to do that here.
