Unfortunately I need to go see my neurologist. I have noticed over the last few weeks that my symptoms are flaring up much more than usual. This usually means a new lesion is causing an exacerbation. When this occurs my limbs experience more pain than normal, which is incredibly uncomfortable.
Right now I am experiencing lightning flash pains in my legs that take my breathe away at times. Also, I have been losing feeling in my left hand, which is a brand new symptom for me. I’ve had hand pain in the past, but I’ve never experienced numbness. The most annoying symptom is the return of the headaches. I don’t want to go back on meds, but I also don’t want to burden Evelina with my constant complaining about the pain.
I never have a Christmas wish list. There’s not really anything I want. I already have everything. All of the meaningful things in life. Two beautiful kids, a loving man, and the best sister. Parents that love me, friends, and a roof over my head. That’s all I need.
Gifts have never been on my priority list. Material things are just things. So when asked what I want for Christmas I usually say nothing or I don’t know. What could I possibly want?
A new leg, a new eye, not to walk like a drunk. Just kidding!
A couple nights ago and like most nights I was unable to sleep. Thanks again MS…lol. I don’t want to keep anyone up with lights or the TV so just like every other night I have nothing better to do but entertain myself with thought. A traffic jam in my brain. Yes I…
Originally posted on MSnubutterflies: When I saw that Jen from Tripping Through Treacle had tagged me in her post about Rocking Motherhood I was a little surprised to be honest. Maybe even wondering what I could add to such a wonderful tag.…
Last night was a rough night. I was in tremendous pain. Getting comfortable at night these days is almost impossible. The pain and stiffness in my legs have made finding a position to sleep almost zero. When I do finally fall asleep I toss and turn. Between the pain and tossing and turning I only get an average of two to three hours of sleep a night. I’m up usually by 1 am unable to go back to sleep.
That’s not what this post is about though. I’ve become kind of used to this nightly process.
This morning I thought to myself poor Greg! It doesn’t only affect me. It affects his sleep and his day as well.
I toss and turn not only moving the entire bed but most of the time I am unable to turn myself. This means I have to grab him and even wake him…
I started taking Ampyra (the walking pill) the middle of August. Today I read an article in Multiple Sclerosis News Today discussing the merits, advantages, and the efficacy of Ampyra. As with any medication, it works for some and not others. A friend was in the clinical trials for the drug, but it didn’t work for him. I have been very pleased with the results I am seeing. Here are a couple of entries from my blog that discussed the immediate results.
9.7.16 I told you three weeks ago how the new medication, Ampyra, was working for me. I continue to see good improvement. As living with MS goes, I have good days and bad days, but I definitely see great strides.
However, it’s like learning how to walk all over again. You know how you walk with your heel hitting the ground first and then you roll…