Hi there, I hope my questions are not too silly, I am just trying to wrap my brain around some things. To be fair, and honest, we do not have a diagnosis yet so maybe I should not even be posting here, please tell me if I need to leave. Our neuro has told us he is confident my husband is facing...
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Hi folks, so happy to have found this sight after searching for info about my diagnosis of PLS in July. First off, if this is in the wrong forum please let me know.
So, before I ask any questions let me give you all some history. I'm 46, male and in all other aspects very healthy. About 2 1/2...
Hello all.
My name is Janelle and I have recently been diagnosed with PLS. I am techno challenged, I've never joined a group like this before so please accept my apologies now for future stuff ups😃😃
I have limited use of my right side and have done for about three years but was only diagnosed...
Good afternoon, all! Well, I’m now over a year in the diagnostic process and just yesterday (following gallons of blood work, MRI’s, EMG’s and NCV) I have received a “working” diagnosis of PLS from the head of an ALSA clinic He was very clear that this is a “working” diagnosis only to the...
Hi Everyone,
I read through the difficulty breathing post from July, but have a couple of additional breathing related questions.
I was given a provisional PLS diagnosis in July after presenting with bulbar symptoms with no LMN findings on two EMGs. (dysphagia, dysarthria, clinical neck...
Here’s where I am at 3 years with my PLS:
• 2009
o Started in left leg, then right (foot drag, falls)
• 2011 – June – Diagnosed
• 2012
o Started using a cane
o Hands next –weakness and fist clenching at night – wear braces for this
o Emotional lability (laughing and crying episodes)
o...
I don't know if it's normal to feel so angry and scared about my PLS diagnosis, but I am. Before my diagnosis I had "undefined symptoms", but since my PLS diagnosis in March I feel like my world, at 47, has come to a screeching halt. Gone are my career, some of my hobbies and many of my future...
Hi all,
I posted on the DIHALS board about a month ago about a possible UMN disorder. Since that time, I've received confirmation that I do have some type of UMN dysfunction, likely either HSP or PLS. The other big suspects have been ruled out at this point. My main problem is spasticity in...
Basically, what kind of neurologist do you see?
Currently the neuro I"m seeing is a migraine specialist, in the general neurology clinic. Which is ok for my cluster headaches, he's the one that was able to diagnose them and is working around with my meds to try to get them under control...
Dear All,
I hope I don't bother you with my long story, but I am looking for help! Hopefully I posted this in the right category!
I'm a woman from 21 years old and I live in The Netherlands. I am desperate and I need some help. What's my story? The problem started when I was about 15 years...
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