Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
I also experience awful "twitches" in my sleep. My whole body will jerk forward and wake me completely up. I have also had those "falling" feelings only I am "ducking" from being hit by a ball in the head...it all happens in a split second, but the effects take a couple minutes to getover and get back to sleep.
You're not alone dear...I'm fighting right along side ya! HUGS
Thank-you, both of you, for your responses. You have no idea how much better I feel.
Oh, one last thing. Today I was driving downtown to pick up perscriptions and saw the large white buildings way up ahead. I don't recall ever seeing them before, but the closer I got, the more I realized (from the looks of them) that they've been there for a long, long time. Did I forget that they were always there? I couldn't have seen them for the first time as I have lived here for 20 years and driven down this street more times than I can count. Very strange. I decided I better see the eye doctor. After a very thorough exam, eyes were pronounced wonderful (which is very good), but no explanation for the 'new' old buildings! I feel like I am losing my mind. I need the kindergarden naps and story time too! Being an adult, especially one with MS, diabetes, and asthma is sometimes just too hard!
Michelle
I have also experienced a kind of dyslexia with numbers, words and trying to find my dang car. I also find myself misreading signs and billboards--some are really funny. A lot of this is just a symptom of ageing, and not neccesarily the drain bamage from MS.
Michelle
I will know exactly what I want to say when I start the sentence, but by the time I am in the middle of it I will lose ability to recall words to finish the sentence. For instance, yesterday I was trying to tell someone about kids coming to the door for a school fundraiser... in the middle of the sentence I could not remember the word "fundraiser."
Having been told I am pretty articulate throughout my life, this is a stunning blow to my self-confidence. I feel it makes me look like an idiot. Then, once I am flustered, NOTHING out of my mouth comes out right!
I am finding that I am much more distressed by my cognitive losses than my physical limitations or even the pain. It takes much longer for me to comprehend what I am reading, and that has always been one of my strongpoints too, quick reading comprehension.
It's tough to share this with some of my family and friends without thinking they wish I would stop whining. I try not to "whine," but it is troublesome. I appreciate being able to come to this forum for understanding support.
I know what you mean about the cognitive function. I've had similar issues. I teach four sections of public speaking to high school students and one block of English I. Imagine trying to teach kids to give speeches and you can't find the words! Fortunately, my students know I have MS and I've forwarned them that this (loss of word retrieval) may happen. Generally someone will supply the word for me. Humbling at first, but now I think it's kind of neat to get assistance from a student.