Tracheobronchial AL Amyloidosis

This topic contains 2 replies, has 2 voices, and was last updated by  duncan 10 years, 8 months ago.

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  • Author
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  • #113790

    duncan
    Participant

    Hi all,

    I know we are few in number, either newly diagnosed or veteran, always nice to and willing to share info and experiences.

    If your new and searching i know there is not much information around, its not all  doom and gloom ,try to stay positive

    I wil get an email if anyone posts, i will get back to you so do not worry if this is an old dated post .

     

     

    #113810

    blessthischick
    Participant

    Hello Duncan

    Just wondering if you have heard of Amyloidosis Awareness on Facebook? It’s a great site with links to other ones. I am being checked regularly for Al Amy after the found some Amy tissue in my skin. Take care.

    🙂 x

    #113881

    duncan
    Participant

    Hi,

    Thanks for the post , no i hadn’t , i go to the royal free every  6 months and a cardio thoracic surgeon lasers my out in plymouth on a regular basis.

     

    Thanks for the info on Amyloidosis Awareness on  face book i will check it out.

    Bye for now

     

    Duncan

     

     

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