User Tag List

Likes Likes:  0
Page 1 of 2 12 LastLast
Results 1 to 10 of 38

Thread: Wegener's Granulomatosis Studies

Hybrid View

Previous Post Previous Post   Next Post Next Post
  1. #1
    Join Date
    Mar 2009
    Location
    Swift Current, Saskatchewan, Canada
    Posts
    6,076
    Post Thanks / Like
    Mentioned
    21 Post(s)
    Tagged
    0 Thread(s)

    Default Wegener's Granulomatosis Studies

    Phil Berggren, dx 2003

  2. #2
    Join Date
    Feb 2013
    Location
    Israel
    Posts
    4,160
    Post Thanks / Like
    Mentioned
    36 Post(s)
    Tagged
    0 Thread(s)

    Default

    Hi Phil,
    thanks for sharing
    poor families
    it is scary to think that our children are in risk of developing WG
    I think that in my case there can be some genetic basis because my parents are relatives....
    Alysia
    dx 2008


    Here, in this forum, I have found my sweet eternal love, my beautiful Phil.. :
    https://www.wegeners-granulomatosis.com/forum/threads/4238-pberggren-memorial-thread
    "You are my sunshine", he used to sing to me... "you make me happy, when skies are grey" I still answer him.
    Rest in Peace, my brave Batman and take care of your weggies from heaven, until we meet again.

  3. #3
    Join Date
    Mar 2009
    Location
    Swift Current, Saskatchewan, Canada
    Posts
    6,076
    Post Thanks / Like
    Mentioned
    21 Post(s)
    Tagged
    0 Thread(s)

    Default

    Alysia, your parents are relatives? In what way?
    Phil Berggren, dx 2003

  4. #4
    Join Date
    Feb 2013
    Location
    Israel
    Posts
    4,160
    Post Thanks / Like
    Mentioned
    36 Post(s)
    Tagged
    0 Thread(s)

    Default

    Quote Originally Posted by pberggren1 View Post
    Alysia, your parents are relatives? In what way?
    they have same grandfather 5 generations back.
    Alysia
    dx 2008


    Here, in this forum, I have found my sweet eternal love, my beautiful Phil.. :
    https://www.wegeners-granulomatosis.com/forum/threads/4238-pberggren-memorial-thread
    "You are my sunshine", he used to sing to me... "you make me happy, when skies are grey" I still answer him.
    Rest in Peace, my brave Batman and take care of your weggies from heaven, until we meet again.

  5. #5
    Join Date
    Mar 2009
    Location
    Swift Current, Saskatchewan, Canada
    Posts
    6,076
    Post Thanks / Like
    Mentioned
    21 Post(s)
    Tagged
    0 Thread(s)

    Default

    That makes them 4th cousins. That is fine.
    Phil Berggren, dx 2003

  6. #6
    Join Date
    Feb 2013
    Location
    Israel
    Posts
    4,160
    Post Thanks / Like
    Mentioned
    36 Post(s)
    Tagged
    0 Thread(s)

    Default

    my syster has Icthyosis which is genetic skin disorder.
    Alysia
    dx 2008


    Here, in this forum, I have found my sweet eternal love, my beautiful Phil.. :
    https://www.wegeners-granulomatosis.com/forum/threads/4238-pberggren-memorial-thread
    "You are my sunshine", he used to sing to me... "you make me happy, when skies are grey" I still answer him.
    Rest in Peace, my brave Batman and take care of your weggies from heaven, until we meet again.

  7. #7
    Join Date
    Mar 2013
    Location
    Almerķa, Spain
    Posts
    299
    Post Thanks / Like
    Mentioned
    1 Post(s)
    Tagged
    0 Thread(s)

    Default

    Good researching Phil, keep it up and we my resolve the mystery to WG
    My blog: Animo

  8. #8
    Join Date
    Jul 2013
    Posts
    14
    Post Thanks / Like
    Mentioned
    0 Post(s)
    Tagged
    0 Thread(s)

    Default

    Is Wegner's as rare as what the medical profession and the researchers say it is or is it becoming a little too common? The specialist that treated my son also told me that more than likely it was genetic but could not tell me exactely

  9. #9
    Join Date
    Oct 2011
    Location
    near Phx, AZ
    Posts
    1,809
    Post Thanks / Like
    Mentioned
    7 Post(s)
    Tagged
    0 Thread(s)

    Default

    WG is rare in comparison to cancers, etc. I've heard all kinds of stats, but most seem to be around 1 in 30,000. Unless, of course, you live near Phil...he attracts Weggies! The amount of 'newcomers' on here indicates a rise in awareness for sure, maybe in actual illness too. But, awareness, due to some on here and some national exposure, of AIs in general and WG specifically, has gone up, but it's nowhere near the heights of financial and research support of many other more common diseases. Genetics are brandished around cuz no one really has an exact idea of where WG comes from...so blame it on the family!!! LOL!
    Knowing how to think empowers you far beyond those who only know what to think. -NdT


  10. #10
    Join Date
    Jun 2013
    Location
    Newcastle upon Tyne, England
    Posts
    39
    Post Thanks / Like
    Mentioned
    0 Post(s)
    Tagged
    0 Thread(s)

    Default

    According to the National Health Service website around 500 people each year are diagnosed with Wegener’s in the UK. It is estimated to affect 3 out of every 100,000 people globally. According to my rusty maths that means over 200,000 people are suffering with Wegener’s right now.

Page 1 of 2 12 LastLast

Bookmarks

Posting Permissions

  • You may not post new threads
  • You may not post replies
  • You may not post attachments
  • You may not edit your posts
  •