← Return to Is this ALS or not?

Discussion
scaredone9088 avatar

Is this ALS or not?

Brain & Nervous System | Last Active: Jul 31 6:57am | Replies (8)

Comment receiving replies
Profile picture for Zebra @californiazebra

That must be so scary for you. Have you seen a neurologist and had nerve testing? Result?

I thought I had ALS ten years ago at 56 when suddenly I couldn’t eat anything without aspirating, trouble chewing and controlling food in my mouth, trouble swallowing. I lost 25 pounds in a month as I became afraid to eat and was just drinking protein drinks. My heart started flipping out from rapid weight loss and lack of food. Two month wait for a neurologist. I already had a history of massive fasciculations, muscle cramps, numbness, tingling, dizziness, legs stop working on stairs, random shooting pains, RLS, pain from pressure when resting my legs on something, fingers quivering, toes started going crazy like a player piano, etc. I already knew I had a rare hereditary neuropathy with pressure palsies (HNPP) but the sudden non-stop dysphagia (occasional in the past) scared me. I didn’t have the drooling but sometimes when I’m chewing something it gets too saucy so I can’t control the food and spit it out. I had the EMG/NCS testing that’s been abnormal since I was first tested at 21 (now 66). I was also tested for MS, myasthenia gravis as my chewing muscles (and other muscles) get weak and fatigued easily. In the end two different neurologists working together ruled out ALS, MS, MG and determined it was still part of my HNPP although the dysphagia is not typical with that, it’s possible. My son has HNPP too (diagnosed w/genetic testing) with some similar and some different symptoms. He has some swallowing difficulties but different than mine.

You definitely have something neurological going on, but there are so many different neurological disorders that have bizarre symptoms that I hope this gives you hope that it may not be ALS. Are all of your neuro symptoms new or do you have a history of some?

Please see a neuromuscular neurologist if you haven’t done so already. 10 years later I still have the dysphagia ( and all the other stuff) but know which foods cause the most issues, keep my head tipped down when eating to avoid aspiration, etc. Frustrating and life altering but not deadly. Prayers for you. ❤️

Jump to this post


Replies to "That must be so scary for you. Have you seen a neurologist and had nerve testing?..."

ALS (or Motor Neurone Disease which we call it in Australia) is diagnosed by a process of elimination. There is not one test for ALS, your neurologist has to eliminate other possible
causes of your symtoms before making a diagnosis. I was diagosed two months ago, and while
initially a shock I am now exploring possible treatment options by discussing them with my neurologist.Please don't believe everything you read on the internet or support group. Some people have some very strange and useless ideas. Trust your doctor, not some weirdo who posts "cures", especially if they ask you for money.