biopsy

  1. E

    I have read the sticky note but I still need your help

    Hello everyone, I want to give a warm tight hug to all of you suffering from this disease. Just give you a long hug with love and love... just love and silence. I cannot find my words... -------------------------------------------- I need your help and will try to be short... this summer...
  2. A

    What is a relevant symptom and what is not?

    I am a 59 year old, caucasian woman. I am awaiting an appointment with an ALS specialist. Thinking back, I had weakness in my left arm as early as Jan. 2014. In May 2014, I had an event that included dizziness (felt like I was banking to the right all the time) and, after a week, tingling in...
  3. Nuts

    Celiac Disease

    I've hesitated about posting this just yet because I'm not sure that I know what to do with the thoughts and emotions that it's caused me. At our last clinic appt, D r Bedlack told us that because of a recent ALS Untangled review on Celiac Disease, he is now testing everyone for it when they...
  4. Rhonda J

    So many mixed emotions....I am a horrible person

    My husband has had this horrible disease for 6 years. He is 57 and I am 50. We have been married 11 years. He is a 25 year Retired Veteran of the Air Force. It came on fast, it took his voice and his walking first...then gradually he has declined to the point of being in a wheelchair 12-14...
  5. R

    Was on here a year ago and need your further advice

    Dear All, I had written on the forum around a year ago regarding some symptoms that i had developed, in a nut shell it started off as weakness in my arm and leg and then progressed into twitching all over my body, flash forward almost a year ahead and i can't really say if its gotten much worse...
  6. T

    It's not always ALS

    So I've been at this process trying to get a diagnosis for three years now. It's been a hard road. I am still in the Army and have been for 17 years. My disease process and diagnosis has literally been all over the place! I'm no faker or malingerer, quite the opposite. I was used to running five...
  7. D

    Someone recognizes my story? Serious muscle problems since 8 years.

    Hey guys, I follow this forum for about a year now and didn't know if I should post my story in this topic, but I am a little concerned. Good thing to know: I do not think I do have ALS, but clinical research shows high neuron problems, they thought it was suspicious. Clinical research is...
  8. Nikki J

    Precision medicine still enrolling

    They are not yet fully enrolled Precision Medicine Program | ALS Therapy Development Institute You have to travel in Boston and they do not pay for the trip or lodging. It is just a few hours visit. Medical history blood draw and skin biopsy. Every month you fill out the functional rating...
  9. Nikki J

    Update on the skin biopsy study

    That KCAE linked in the retigabine thread. The listing was old but now updated ALS Clinical Trials | ALS Clinical Research | The Northeast ALS Consortium (NEALS) Anyone in the Boston area or visiting should look into it. If you are on blood thinners, have a history of keloid formation or are...
  10. karla r

    opinions from people who know.. kinda scared

    Hi, just wanting to know if my doctor is on the right track, or if I should maybe look for a new doctor. I guess cause I am a little scared. Here is what happened. I noticed numbness and problems with my leg, first the right. Originally, they said after tests. I had had a minor stroke. September...
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