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  1. S

    Wait and see approach

    Hi Everyone, It's been a while since I've last posted and not a lot has changed since (diagnosis wise). I really don't want to bother you with a huge list of symptoms, nor do I want to come across like a huge worry wort, when my concerns are many of your realities. So I'll try and keep it as...
  2. M

    Dental Care

    My PALS has exceeded his life expectancy, for which I am grateful. He is on hospice care at home. He has not had oral care in about a year and I am concerned about tartar buildup and also the fact that occasionally he grinds his teeth after yawning. He has bulbar onset. He is unable to hold...
  3. mydecember1985

    Old thread was closed. 6 months of twitching, cramping, etc.

    Sorry I hadn't logged in for some time. Original thread here: https://www.alsforums.com/forum/do-i-have-als-als/38134-my-story-after-6-months-twitching-cramps-maybe-some-foot-drop-suggestions.html Mods please combine it back if possible.:mrgreen: <Sorry. See my post below. --mod> My...
  4. A

    Any Ideas??

    I'm trying to figure out who to turn to if none of my symptoms appear to be ALS. Please check my history below. If you have a recommendation or another forum, please share. I do see my neuro again on August 10. We will be discussing meds. March 2011 -Electric Nerve pain in feet and hands...
  5. J

    Old thread closed. Slight update Jay654

    Hello again guys, Haven't posted for a while as I wanted to kind of ignore all symptoms and things that possibly pointed towards ALS/MND & give my mind a rest. Have now seen both Professors, they aren't finding any upper motor neuron signs but have noted the constant twitching mostly localised...
  6. A

    i don't know if i have ALS or not, panic attacks because of that.

    i'm 21 years old. (I learned english by my own, so i apologize for any mistake) 2 months ago i had an Arrhythmia for like 4 days. After that, i had a problem in my neck, it was hard stand my head with my neck, and that came with Dizziness (it stoped after a week) Now, i've had fasciculation...
  7. S

    Still here, waiting in limbo land..

    Hi everyone, I posted a little while ago (March, I think). I was waiting for my EMG, which I had on the 1st April. Since my last appointment with my neurologist my symptoms progressed some more, more weakness and atrophy in left foot and hand and a cluster of pyramidal signs. Due to the...
  8. H

    Familial Versus Sporadic

    Hello, Thank you for allowing me in your group. My sister was diagnosed in 12-12-13, she passed 5-4-15. There are 7 children total, a brother died at 22 months unrelated to ALS, all in relatively good health. My mother is adopted. Both parents 86, still living and in relatively good health. My...
  9. T

    Symptoms that are hard to ignore

    Thank you for having a place to ask these questions. I have a deep sympathy for people that are suffering. Now I think I might be one. I'm not sure where to start, but ask that you please be patient with me. I have researched over and over again the symptoms I am experiencing and it leaves me...
  10. J

    This is ruining my life.

    Als as a 23 y/o female? I really need someone who has personal experience to calm me down a bit. The worry is starting to ruin my life. Let me first say a few things. 1. I totally understand that many of you are struggling on a level that I can't possibly understand. Trust me when I say I'm...
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