Hello folks!
Just wanted to do a restart from three years ago. The last 3 to 4 years are very blurry. I’m much better now.
Other than my Ig infusion twice a month and I am super challenged when attempting to walk…all is well in my camp. I’d love to interact with some of you. I hope to hear from you.
But God is sufficient.
Happy that you’re back, robster1 ! I find that time gets away from the best of us! I look forward to seeing more of your posts! 
Thank you dear friend!
🤗
It’s good to hear from you. I’m sorry that you have had a difficult time. It’s definitely part of the disease. Welcome back, we missed you!
Tell me about IG infusion -no steroids? Glad you are doing well
I had a terrible time with ulcerative colitis and three bouts with C-dif. It about killed me! Messed my immune system up. I was doing the Ig infusion once a week for over two years. Then my neurologist cut me back to two infusions on one week every month.
The actual name is Immunoglobulin replacement therapy. Look it up. Let me know your thoughts. Thank you!
This might be a post for another day, robster1 . There are many in this forum that would benefit from your experience, and it would bring a spotlight on this. Stay on the road to your recovery.
Thank you friend.
Glad you are back!!
Thank you!
Welcome back!
I certainly hope that after the blurry years you are in a better place now! Sometimes it seems that when we go through hard times and come out the other end, things are much better.
Glad you are back!!
Welcome back, roster! I stumbled upon this wonderful group in early 2021. Guess I missed you. I agree - God is sufficient!
Welcome back glad all is well
Happy 4th MSers.
I have PPMS.
new treatment 
MS Community
Better day today
