It's very frustrating to have so many things going wrong and no answers. I'm still there, and it looks like I will be for a long time unless my brain shows up having a lesion someday.
I have had slurred speech off and on, and mine also comes on with the tightness in the throat and under the tongue (digastric spasms). There are some intermittent word searching problems, and feeling of being tongue tied. Then there have been a few times where the first sound of the words have come out multiple times before I could finish the words.
For years, before every Christmas (I correlate this with stress) I would have problems stuttering. That was always my cue to slow down and try to relax. After the holidays, it usually went away until the next holiday season. Stress. That's my excuse for everything all along. Until now when it all hit at once.
I have intermittent slurred and or stuttery speach, i do not feel anything different so i dont have any warnings. I can be talking quite normally, which now includes intermittent loss of nouns, and out of know where a word will elongate or be strangely pronounced or be impossible for me to pronounce. It is deffinetly more likely to happen if i am dealing with fatigue but other wise there is no warnings.
Have you been assessed for epilepsy or one of the types of migraine?
I have intermittent slurred speech. Embarassing! I feel as if I have a mouth full of bubble gum & can't get the words out! At times my mind & mouth don't work together! I will say things/words backwards.
yes I have been dx with simple partial seizures because the doc. believes my brain is misfiring and getting stuck for two weeks...
I have had the slurring speech come on out of nowhere before but it was like 16 years ago and i called it my lazy tongue. I was reading out loud to my consumers at work and my words started to come out all slurred and i sounded drunk. Back then it was short lived, maybe a day.I never looked into it,,, never said anything to my GP either, I was young and I thought it was normal . Who Knew>???
Do your facial muscles start to tighten up when you slur, and how long does it last
I've never had slurring, but I have had an almost lisping problem, a bit of a whistle.
That was pointed out to me by a doctor, not a neuro, who knew me well. It was years before my MS diagnosis. I was having numbness and tingling in my mouth on the left side, along with several neck problems.
Fortunately, it went away after a few weeks, and ultimately the other neck stuff resolved. These haven't returned, knock on wood.
I am going crazy over this whole slurred speech thing . It has been my recurring symptom over the years
.During each of these times I experience something new througout the year. And it lasts longer each time
First time I had slurred speech,, I had two "dead" legs while lying in bed during that year, can't remeber how long after it happened, but that lasted throughout the night.( not on the same day though)
Second time, I had it, I also had a stiff neck come on outta nowhere while I was in a stressful meeting at work. I started to get pain in my neck and whamo, STIFF neck and cant move it for a month.
Third time, I had just got done having Radio Active Iodine treatment for my thyroid and I Became very very sick, I felt like I was dying .. i was told I could have slipped into a coma. It was bad and the slurred speech lasted for a week. I was extremely fatigued, muscle weakness in arms and legs. Pain in wrist that became very stiff and I couldn't move it for a week.
Fourth time: 4 months after surgery, I was very stressed about losing my job, and health insurance, disability checks from work were ending and my optic nerve specialist would not release me to go back to work, not that i could anyway but I was absolutely devastated,
This tiime I slurred for a week and a half. EACH EPISODE GETTING LONGER. Symptoms started up big time this year during this same year and another surgery, I had Lightheadedness, poor memory, word searching , ground sinking in when walking, very off balance, double vision getting worse, optic nerve damage appeared worse, dx, with nystagmus, bulge disc in c5/6, depression, noise intolerance and found out I was vit. d deficient
5th time: Waiting on lawyer about SSD and he was very mean to me!!! and Again 4 months after my surgery slurred speech for TWO WEEKS. Along with more odd symptoms to follow throughout the year. Twitching, cramping, buzzing, itching, some numbing but not bad, eye twitching (nystagmus) always when trying to focus or tired. Facial pain, foot pain, stabbing random pains all throughout body. and my list can go on and on;;;; how could these dr.s not see the obvious. OMG
I am soo sorry everyone for my rant, I guess I needed to get that out!!!!!
i am feeling very "out of it " today, and I dont know why
I haven't had any show on my brain either. I had an mri on my cervical area but was not looking for ms it was to look for a bulging disc,, I don't know if it can be seen without looking for it. After my reflexes showed they were hyper, the nuero ordered an mri of the lumbar spine and still nothing showed.. My last step is most likely a spinal tap.
i get slurred speech, almost every episode over if i over do it. it is embarrassing. face tingles, twitches and tongue and lips feel heavy or numb. then blotchy vision off balance and then i walk funny. scary stuff. my brain has periods where it doesn't think right my episodes were shorter and symptoms were less strong now after 1 and half yrs the symptoms are way more severe and scarier by the minute. i feel for you and you are not alone!
I sounded as though I was drunk. My tongue felt thick. I could tell that I was beginning a relapse, but that was a new symptom. Frome time to tim, my face goes numb or my trigeminal nerve goes crazy. This was mostlly un-related. I drives me crazy too.
I know the neuros always pin point speech slurring on TIA's or seizures, however, I have a problem with the whole two week long episode,, I believe they think they passify the patient with a dx just to shut them up for a while until the lesions show up.
I have read about the medicine for seizures can also help control or keep the flare from progressing , also, I have read that when a dx cannot be made, a doc. will say its a ministroke because the treatment is an aspirin or (AGGRENOX) that's what I was on.
Fibromayalgia is another one that gets thrown out there along with Chronic Fatigue Syndrome. They are an easy dx, instead of doing the research and find out the underlying cause for the pain, twitching , slurring and fatigue.
I am certanily not a dr. but I have brought this up to some of my 13 drs. and my physchologist and they kinda smirked and had to agree with me.
I believe what I was feeling was the beginning of a relapse and not an aura to a seizure.
This is sooooooo crazy.
I had it and could tell mostly when it was going to happen so I would pause if I was speaking, or stop altogether. During those same pre-slur/slowed sensations (i'm clueless as to what to call them) I lost my ability to write as well.
If I remember correctly, the ability to understand but not speak of write it specifically "expressive aphasia." It is considered a major cognitive finding in Neuro Trauma patients and is pretty common in coup contrecoup brain injuries. This is very specific to a lesion or lack of blood flow in Broca's area of the brain. I seem to remember that many stroke victims have expressive aphasia and one of the "work arounds" was to sing what you are trying to say. Singing uses a different area of the brain to form that expressive thought (left brain - right brain issue.) This was a big area of research in functional MRI. Maybe a search under expressive aphasia will yield some more ideas. As people of the forum write stuff, the weirdest stuff comes back to me.