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405 total results
Comments (350)
Hello Brandon (and others). First of all, I am so sorry to hear about your symptoms....
https://connect.mayoclinic.org/comment/830752/
, I am so sorry to hear about your symptoms ... I share a lot of your symptoms, but ... I am not worried about ALS at all because ... very much, which tends to rule out ALS ... ALS is far more rare though.
I would ask the doctor about electrolyte levels, too (PCP or neurologist). Sometimes fasciculations "just happen"...
https://connect.mayoclinic.org/comment/826653/
not have reduced the fasciculation symptoms ... big, well known things (particularly ALS
If your CO2 is at 51 or higher, the Trilogy 100 (or equivalent) VENT- is better...
https://connect.mayoclinic.org/comment/800661/
have specialists at UAB Birmingham, AL ... don't understand my complicated symptoms
Thanks Teresa for answering. Yes I think a second opinion is a good idea but my...
https://connect.mayoclinic.org/comment/790245/
they feel its confusing how these symptoms ... they are going to treat it like it is ALS
Hi @kathy115 I’m so sorry for the delay in responding to you! I was on the...
https://connect.mayoclinic.org/comment/764843/
diseases-conditions/myelodysplastic-syndrome/symptoms-causes ... information with a little video from Dr Al-Kali
Have had fasciculations in my tongue and calves mostly. Also trouble with slurred speech and swallowing...
https://connect.mayoclinic.org/comment/752445/
Obviously ALS on my mind but no weakness ... just wondering if anyone had these symptoms ... Really worried about ALS with these ... symptoms.
@westcom I am a spine surgery patient for cervical stenosis. I wanted to share some information...
https://connect.mayoclinic.org/comment/739960/
with your lumbar spinal stenosis and symptoms ... mimics a spine problem adding more symptoms ... 46-year-old female who experienced symptoms ... ilioinguinal nerve. – Doubleday et al
Hello. I am new to the forum and like most very scared and concerned. I am...
https://connect.mayoclinic.org/comment/738775/
researching google and found something about Als ... This started me reading about symptoms ... emg and have other signs if you have Als ... physical and on emg studies regarding als
Update: I stopped taking Lyrica after switching to Tegretol, a seizure medicine I had taken previously...
https://connect.mayoclinic.org/comment/733653/
Dysautonomia Clinic in Birmingham, Al ... for all these frustrating autonomic symptoms
Hi @amfb, Welcome to Connect. My PMR is in remission now but the two times it...
https://connect.mayoclinic.org/comment/725225/
I als found a study that discussed the ... You might want to keep a daily pain/symptoms
I gave info on the fact that testing is interpreted differently by different doctors. Number of...
https://connect.mayoclinic.org/comment/695830/
Lyme (LLMD's, ILADS, Igenex et al ... negative, but they treat anyway based on symptoms ... In the end, I accept my chronic symptoms
Hello @patzmar, Welcome to Connect. My Mayo Clinic rheumatologist who diagnosed my PMR started me at...
https://connect.mayoclinic.org/comment/686805/
been noted anecdotally to bring good symptom ... On the other hand, Kremers et al,32
@ecann32 Hello and welcome to Connect. I am a spine surgery patient and you said several...
https://connect.mayoclinic.org/comment/670683/
things that caught my attention as symptoms ... My first symptoms of cervical stenosis ... He had ALS, and I could see muscles ... I had worried about ALS too, but what
I'm glad I found this thread. It was beginning to feel like I was the first...
https://connect.mayoclinic.org/comment/653428/
world to have this combination of symptoms ... My symptoms were only numbness in my ... I thought for sure I have ALS and I
@amybeau, hello. I got my Pfizers in Dec/Jan. I quickly (within a week) began having burning...
https://connect.mayoclinic.org/comment/636827/
experiencing localized pain to these other symptoms ... Al my life I’ve been pretty fit and
Hello @johnsmith1980, Welcome to Connect, an online community where patients and caregivers share their experiences, find...
https://connect.mayoclinic.org/comment/613755/
with BFS fear that it can turn into ALS ... Anyone who is uncertain of their symptoms ... -- Amyotrophic Lateral Sclerosis (ALS ... /connect.mayoclinic.org/discussion/als ... genes as someone in the family with ALS
Yes, he has had PN diagnosis for 15 years or more...vague symptoms at first. No Family...
https://connect.mayoclinic.org/comment/610138/
diagnosis for 15 years or more...vague symptoms ... Was also misdiagnosed with ALS in 1995
Hi Helen, Not knowing is not being stupid. In my case, I am very toxic with...
https://connect.mayoclinic.org/comment/606147/
My first symptom was, since 2013, unending ... Sclerosis, or Lou Gherig disease (ALS.org
I don't post very often but have been following al the posts re: neuropathy worsening. And...
https://connect.mayoclinic.org/comment/335467/
very often but have been following al ... are not doctors but sounds like more symptoms
@ellenn I've coughed up about 2-3 TBS blood twice over the past 3 years (a combination...
https://connect.mayoclinic.org/comment/330703/
mornings, but don’t really have any other symptoms ... MAC lung disease" by Gochi et al
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