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  1. J

    Could this be ALS

    I also get the hiccups every time I eat or just out of the blue. I don’t know why
  2. J

    Could this be ALS

    Some of you may remember me. I’m sorry for my prior posts I got frantic. I am still having twitching in my upper arms. It’s hard to use my arms and my right shoulder is bone it’s hard to sleep and use my arms. Does anyone know if an arm EMG reads the shoulder? Or just the arms. Thank you in...
  3. J

    Looking for opinions

    Al, it looks like you are correct. The abnormal brain lesions seems to point to MS. I’m getting a spinal tap and more blood work. Thank you all for putting up with all of my messages. Your the most courages people I have ever come across. Im not looking for responses. Go’s bless you all. And...
  4. J

    Looking for opinions

    I did not mean to offend anyone at all, apologizes. Your right I’m scared because I can’t control what’s happening. I just posted to vent I did not mean any harm. I didn’t think anyone would reply or pay attention. I’m angry because of what’s happening and didn’t know where to go to vent...
  5. J

    Looking for opinions

    My classic ALS symptoms go on and on, my body is rotting and I’m so angry,,,,, so I’ll be back when I get official diagnosis so I can hopefully then get some support
  6. J

    Looking for opinions

    Hi, so my vitamin B12 was 307, all other 11 viles of blood work fine. My right shoulder is now bone. I cannot use arms above elbows. Have to use heating pad around shoulders and back. My tongue besides being horrific looking is swollen it burns and is hard for me to talk. Shoulders lock, very...
  7. J

    Looking for opinions

    If their is anyone that believes me, comments are welcomed but if it’s against the rules (which I believe it is) I understand completely. Thank you for reading
  8. J

    Looking for opinions

    Things are not looking good. I can’t lift my arms up that high, the pain from my neck all the way down to my fingers on the right. It feels like lobsters are squeezing my muscles, I often use my left hand to hold my right arm up because it’s so heavy. The Atrophy on my right shoulder is worse...
  9. J

    Looking for opinions

    Laurie, I’m so sorry that my post offended you. I have not been cleared of anything yet. My neurologist set me up with an appointment to see an ALS nueromuscler doctor due to my shoulder hand Atrophy and tongue appearance , I didn’t post about my ongoing symptoms, was just an innocent question...
  10. J

    Looking for opinions

    I’ve been trying to search for (going through diagnosis) support group. I thought it would be healthy to join a formum for people with similar symptoms still in the diagnosis process like me. Does anyone have any idea if there is such a forum? I’m not able to find one, was wondering if anyone...
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