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453 total results
Comments (390)
You have really weathered a helluva neuro storm—and still are. To a lesser extent, so am...
https://connect.mayoclinic.org/comment/1076436/
checked—and correct me if I’m wrong—ALS ... which means it doesn’t cause sensory symptoms
Welcome @mimi4968, I moved your question about new treatments for AL amyloidosis to this existing discussion:...
https://connect.mayoclinic.org/comment/1067446/
question about new treatments for AL ... discussion:
~ Recently diagnosed with AL ... /connect.mayoclinic.org/discussion/al-amyloidosis ... search=Amyloidosis
AL (primary) amyloidosis ... reduce amyloid production and control symptoms
With my Sister, her diagnosis of ALS, began to appear as something similar to a stroke:...
https://connect.mayoclinic.org/comment/1052307/
With my Sister, her diagnosis of ALS ... After her first symptoms, it developed ... If you were told that you have ALS after ... over two years of symptoms, I would
Hello!I have had muscle twitching all over for about 6 months now.I have been ill for...
https://connect.mayoclinic.org/comment/1035306/
My symptoms came on after an iron infusion ... /possibly covid.My other symptoms are ... any virus or infection.Some of my symptoms ... with is Covid.Do you have any other symptoms ... in are ALS,Myasthenia Gravis and LEMS.Maybe
Hi Alecia!Were the Doctors able to give you treatment for your issue?I have alot of twitching...
https://connect.mayoclinic.org/comment/1034711/
weakness.The neurologist told me it is not ALS ... still not sure.I wonder if part of my symptoms
Hi @par4rosy et al. When I first saw this post, I thought the question was asking...
https://connect.mayoclinic.org/comment/1030884/
Hi @par4rosy et al. ... almost right away, and all of her symptoms
P.S.S. Here is the gallbladder link. I sent the ALS link previously in error. You can...
https://connect.mayoclinic.org/comment/1027602/
I sent the ALS link previously in error ... You can read that, too, and your symptoms ... don’t line up with ALS to me. ... www.mayoclinic.org/diseases-conditions/gallstones/symptoms-causes
I do think it would be good to get nerve conduction testing and EMGs to test...
https://connect.mayoclinic.org/comment/1027547/
and try to get root cause of your symptoms ... Try not to worry about ALS until you
Hi @modified82 It’s disappointing to hear you weren’t eligible for an appointment. The criteria for appointments...
https://connect.mayoclinic.org/comment/1009673/
in the forum with a member who has symptoms ... BFS or ALS? ... connect.mayoclinic.org/discussion/bfs-or-als ... another post where a member requested ALS ... said they’re not sure now if it is ALS
Ladydi48, mine started in September too! We have a lot of similar symptoms. I hope your...
https://connect.mayoclinic.org/comment/1003694/
We have a lot of similar symptoms. ... The fear of ALS and PD was real.
@soccer1477 Well the good news here is that it states there is no evidence for ALS...
https://connect.mayoclinic.org/comment/983360/
it states there is no evidence for ALS ... There isn't a specific predictable symptom ... was a bit unusual because all of my symptoms
@monkeytime777 i have this but was diagnosed with hereditary spastic paraplegia complex type. it was found...
https://connect.mayoclinic.org/comment/960922/
channelopathy can also give these symptoms ... a lot of thing it could be besides ALS
I am indeed going to therapy (I've been a therapy regular since I was a teenager)...
https://connect.mayoclinic.org/comment/927030/
into the typical demographics for ALS ... , a clear EMG would make ALS extra unlikely ... anxiety/stress/insomnia/depression symptoms ... It is great to hear that your symptoms ... apparently, it is pretty unusual for ALS
Yes, i am suffering with BFS. Mine started a year ago with twitching in my lower...
https://connect.mayoclinic.org/comment/904729/
My symptoms were getting worse and i ... was concerned about ALS.Saw a neurologist
Hi again Betty. My doctor doesn't know the cause. We ruled out ALS and MS, ruled...
https://connect.mayoclinic.org/comment/903964/
We ruled out ALS and MS, ruled out autoimmune ... it before I stop and just focus on symptoms
@cadabra Hi there! I'm so sorry to hear of all your struggles and worries ... unfortunately,...
https://connect.mayoclinic.org/comment/900562/
but one of the diseases I have is ALS ... -4 (juvenile als - rare type). ... #34;textbook" and have different symptoms ... answers or can better manage your symptoms
As an update, it’s now past one year since my symptoms started. I have been tested...
https://connect.mayoclinic.org/comment/838693/
update, it’s now past one year since my symptoms ... so many different things including ALS
I was recently diagnosed with PN and experience twitching in calves, thighs, and arms (triceps primarily)...
https://connect.mayoclinic.org/comment/828815/
conduction study and was told it was not ALS ... PN can cause the symptoms we’re having
Me! 9x12 mm. Anterior falx…. Under a web of veins of course. Said if did surgery...
https://connect.mayoclinic.org/comment/1284100/
(radio-surgery like gamma knife et al ... it’s calcified & not growing/no symptoms
I would not assume that it is ALS. It seems like that would be an unusually...
https://connect.mayoclinic.org/comment/1302264/
I would not assume that it is ALS. ... However, the symptoms are concerning
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