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415 total results
Comments (359)
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
Hi @alwhite and welcome to Mayo Clinic Connect, an online network of patients. You'll notice that...
https://connect.mayoclinic.org/comment/248644/
burning-mouth-syndrome-very-severe/
Al ... What are you symptoms like?
Hello, Happy to share. The condition is mildly painful but more often than not just very...
https://connect.mayoclinic.org/comment/231014/
You test to rule out MS, ALS, PD, small ... but given time and persistence in symptoms ... Google pointing people to think ALS) ... people posting the huge list of EXACT symptoms ... majority of people noticed the onset of symptoms
On the bright side, I’m a long COVID 2020 victim who is finding help from Dr....
https://connect.mayoclinic.org/comment/1249548/
Jordan Vaughn in Birmingham,AL. ... very significant improvement in my symptoms
I have had 2 experiences with rehab. Each was disappointing. Both were before I had my...
https://connect.mayoclinic.org/comment/1305877/
In fairness, I had no classic PD symptoms ... and overall evaluation by a physi al
Thank you everyone for your support, the ALS is diagnosed at the Mayo Clinic and our...
https://connect.mayoclinic.org/comment/1260919/
you everyone for your support, the ALS ... our cousin is showing more and more symptoms
Hi, I want to share my journey with CLIPPERS, as it is again different from what...
https://connect.mayoclinic.org/comment/857399/
My only symptom was the diplopia, so ... been described in 2010 by Pittock et al
@lydiamay1 I'm so sorry you are so young and caring for a child through such worry...
https://connect.mayoclinic.org/comment/275576/
and joint pains and other strange symptoms ... look the same in both some of the symptoms ... believe MS is Lyme undiagnosed and even ALS ... Disease, as I guess it can have MS like symptoms
First off, best of luck to you keep in mind how nice it will be to...
https://connect.mayoclinic.org/comment/125595/
from 150 a few weeks ago - so far symptoms ... Best of luck to you al and hang in there
Hi, Damien, welcome to Mayo Clinic Connect. It must have been a relief to hear from...
https://connect.mayoclinic.org/comment/263574/
neuromuscular disease - that the diagnosis of ALS ... You list your dad's current symptoms ... your father keep a journal of the symptoms ... seems to cause or correlate with the symptom
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