dying

  1. jethro

    Experience with L-serine

    simple, cheap, accessible non esential aminoacid (except in my country :-( ). can anybody share experience? how much do you take per day? what kind of benefit do you get? this is not a cure, this is retardant. it freezes dying of MN. thats how i got it. havent heard any side effect. what i am...
  2. J

    I never imagined it would hurt so bad....

    Hi Everyone, I lost my beautiful little brother on September 12, 2017. He was 47 years old with 2 young children. i knew I would miss his presence but never imagined this much. I knew what the outcome of ALS was yet still feel so unprepared. My mind keeps going back to those last few...
  3. L

    Scared new mommy

    Hi all, I just gave birth to my son two and a half months ago, and i have been told i have post partum depression, and i have been a little overly worried about dying lately. However, I feel that i have developed symptoms that point towards ALS and i am very scared. Here are my symptoms...
  4. E

    Can't shake the worry...

    So, I just wanted to first say thank you to anyone who comes on here and despite what you are going through tries to put the minds of what are probably many hypochondriac at ease. It's very kind of you to do that... and I hope I am just another hypochondriac. My situation is as follows...
  5. L

    New Mom Searching for Answers

    Hi everyone, This has been a hurry up and wait process and I'm searching for support. I delivered a baby girl via c section 3 months ago. She is my second baby. My first night in the hospital I noticed my forehead muscle spasming. Thinking it was due to stress, I put it off. I was having what...
  6. C

    Anger and sadness

    This is such an ugly and devastating disease. I can literally feel him winding down..beyond heartbroken...how do you come to say your dad and hero is dying?
  7. S

    Doctor assisted suicide

    My dad keeps saying he doesnt want to wake up. He hates that he cant do anytjing but is refusing almost all interventions (peg, walker, scooter, wheelchair, etc... he does have a bipap and cough assist but only uses it about 5 hours at night instead of most of the day as per dr). We keep trying...
  8. S

    First I don't think I have ALS--just need opinions and resources

    I'm 32/female. This all started when I was 15 and has slowly, very, very slowly eaten away at my body. I do not think I have ALS. This is way too slow. My problem areas are all on left side of my body, except for my toes. I haven't been able to wiggle or bend my toes on either foot for about 10...
  9. A

    The end is aproaching

    My sweetheart is actively dying, the prognosis is maybe two more days. I can't stop crying .....This is more then I could imagine, I was praying for mercy because I hate to see him suffering but I miss my soulmate so much... I don't know how I can get on with life. I wish I could go with him. I...
  10. R

    No Answers

    Hello to all. I am thankful for having a forum like this. My dad was dx with bulbar ALS nearly 3 years ago at the age of 72, and I am grateful for every day he remains with us. He is presently on a ventilator but still has control of his arms to write, so he comunicates with us very well...
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