ivig

  1. BlsdMama

    PLS and atrophy

    Mayo found a glycine receptor antibody so I'm starting IVIG to see if I respond. However. Frankly? One of my calves (on the weak leg) has atrophy. It's flat and slack. (My neuro has seen this and gave me an EMG. It was clean.) My foot is my biggest weakness -drop foot. But the inside curve...
  2. BlsdMama

    Glycine Receptor Antibody?

    Has anyone else been tested for this? I was dx'd by the U of Iowa Neurology around April/May-ish officially with PLS, moved to ALS Clinic. Asked for a second opinion in June. Was seen by Mayo in Rochester in July. The PLS diagnosis was affirmed. I was tested for Stiff Person Syndrome (GAD...
  3. C

    update

    Hi, I just want to post. Yesterday I come back after check up with emg specialist. So sumarry: - 2,5 years with symptoms. -Brisk reflex overall -stiffnes in libs( after I take prednisone it`s gone, after stoping the steroids it`s back) -symmetrical muscle atrophy in hads and wrst -summetrical...
  4. E

    EMG Posting

    I am sorry for the delay in responding here. It has a been a hectic few weeks to say the least. Per my previous thread my wife has been diagnosed with "Probable ALS". Here are the EMG results: This was the initial one done by our local neurologist...
  5. M

    MMN or ALS... Waiting game

    Anyone on here have MMN? I'm experiencing muscle fasciculations, atrophy in hands, arms, legs, feet and probably other places I haven't discovered yet. Lately my lips began twitching. Everything twitches all time but the anxiety of the whole thing is the worst. I would love to hear from someone...
  6. C

    I'm Not really sure what to do next??

    Hello to all again... My first post was quite some time ago. 02-15-2014... At that time I was headed to University of Michigan Neurological Dept. for my 1st visit to the ALS Clinic. At U of M I went through a barrage of test, over an 8 month period. I went from possibly ALS, to Possibly...
  7. S

    Fast progressing?

    Hello, Until 3 weeks ago my brother was having IVIG and hoping for a change of diagnosis to MMN as he seemed to be responding to it. However he then developed leg symptoms for the first time (previously it was all finger and arm) - weakness and shaking, difficulty walking. He had a first episode...
  8. S

    als or mmn?

    Hi, My brother was diagnosis with ALS last July and I've been posting here since then – he's young, has a young family, and is the main caregiver/child rearer of the family – his wife works full time. His little kids adore him. Its been very tragic seeing him unable to lift up his little girl...
  9. S

    Medical marijuana

    Hi, I've been posting on here on and off since my brothers ALS diagnosis last July. He's only 40 and has a toddler and a new baby only 8 weeks old. We're all devastated and I've spent a lot of time researching treatments and therapies. His situation at the moment is that he's being given IVIG...
  10. S

    New member with IVIG question

    Hi, My brother has just been diagnosed with ALS. We the family are devastated. He is young with a young family. He has been told he can start IVIG treatment next month. I see that many ALS sufferers on this forum have had IVIG, but my understanding is that it is not appropriate for ALS, but only...
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