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awieleba is on a distinguished road
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awieleba awieleba is offline

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Visitor Messages

Showing Visitor Messages 1 to 10 of 124
  1. writer07
    04-04-2013 06:57 PM - permalink
    writer07
    Dear awielaba,

    I read your 2008 post and your story was very much like mine. Pain the moves around, fairly sudden onset. May I ask how you are doing? Were you ever diagnosed?

    Thanks and hope and pray you are ok
  2. mthapa
    08-29-2012 10:32 AM - permalink
    mthapa
    Hello mam, I have posted a thread yesterday, Suspecting misdiagnosis after 10 years, but haven't received any comment. I really need to know the experience of people whether I am misdiagnosed or not ? I am new to alsforums & don't know how to spread my thread to other members. please help me to get comments from experience members. Thread link: http://www.alsforums.com/forum/do-i-have-als-als/20125-suspecting-misdiagnosis-after-10-years.html
  3. hopingforcure
    10-12-2011 10:33 PM - permalink
    hopingforcure
    Checking in on you pretty lady.. Wondering how you were doing, and let you know I am thinking of you and yours.
  4. SpringOwl
    10-03-2011 12:49 PM - permalink
    SpringOwl
    Oh, BTW., the picture of your left hand looks EXACTLY like mine.
  5. SpringOwl
    10-03-2011 12:47 PM - permalink
    SpringOwl
    Please read the second post first so it will make sense! I didn't realize there was a character limit!
  6. SpringOwl
    10-03-2011 12:46 PM - permalink
    SpringOwl
    I was googling stuff about antibiotics and your post came up that you contracted c-diff from antibiotics a while back.

    I see you were undiagnosed and was wondering if you have lyme or something else. Do you see a particular Dr.?

    I am just trying to learn as much as I can. I too have young children and am hoping for some mobility back.

    Thank you for reading. I hope you are well!

    Amy
  7. SpringOwl
    10-03-2011 12:46 PM - permalink
    SpringOwl
    Hi Awieleba,

    I saw you are located in Oakland Co., MI. I am in Sterling Heights, (Macomb Co.)

    I struggled with a possible ALS diagnosis for over a year and then possible MS for 6 months. I have both upper motor neuron signs like spasticity and an abnormal babinski reflex and also lower motor neuron symptoms like weakness, fasciculations, and atrophy.

    I can no longer walk unaided and have lost the use of my left arm and hand. (I am typing this with one hand).

    I finally became my own doctor and found a Lyme Doctor in Michigan. I had my blood drawn and sent it to IGENEX.

    In June 2011, I tested positive for lyme and began oral antibiotics. I have received no results and am scheduled to receive a PICC line tomorrow. I will be receiving the antibiotic Rocephin.
  8. hopingforcure
    08-21-2011 09:54 PM - permalink
    hopingforcure
    Hi pretty girl.. Wanted to stop in and check on you.. PM me sometime and let me know how things are going.. I sure help well..
  9. olly
    07-02-2011 04:10 PM - permalink
    olly
    hey sweet lady,were have you been hiding?
    saw you dropped in on me.........but no message!
    hope you are doing ok and your beautiful family.
    dont be such a stranger...........take good care.caroline
  10. RohnboSlice
    06-07-2011 06:42 PM - permalink
    RohnboSlice
    Are you still around?

About Me

  • About awieleba
    City
    oakland twp
    State or Province
    michigan
    Country
    usa
    How has ALS/MND impacted you?
    seeing neuromuscular specialist for my issue's
    When were you diagnosed?
    00/0000
    Biography
    married to wonderful man, 3 beautiful kids. 6,4, and 7 months
    Occupation
    was a loan officer, now loving mother & wife at home
    Interests
    golf, tennis, dinner with friends, being with my family
  • Signature
    No diagnosed, still looking and hoping for the best!

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  • Last Activity: 03-02-2013 12:11 AM
  • Join Date: 04-28-2008

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