It appears you have not yet Signed Up with our community. To Sign Up for free, please click here....



Lung & Respiratory Disorders / COPD Message Board

  • Scleroderma

  • Post New Thread   Closed Thread
    Thread Tools Search this Thread
    Old 11-10-2013, 05:23 PM   #1
    IN Resident
    Newbie
    (female)
     
    IN Resident's Avatar
     
    Join Date: Feb 2010
    Location: NW Indiana USA
    Posts: 3
    IN Resident HB User
    Scleroderma

    My husband has Scleroderma which has caused pulmonary fibrosis. He is achy all the time and has been on oxygen for 2 1/2 years. Can anyone contact me if you have suffered or know someone who has this condition so I know what we can expect?

    Please! I need more information. Doctors are not really saying. They want him to continue being a guinea pig and keep taking medication. So far no meds have worked and we already know there is no cure.

     
    Sponsors Lightbulb
       
    Closed Thread




    Thread Tools Search this Thread
    Search this Thread:

    Advanced Search

    Posting Rules
    You may not post new threads
    You may not post replies
    You may not post attachments
    You may not edit your posts

    BB code is On
    Smilies are On
    [IMG] code is Off
    HTML code is Off
    Trackbacks are Off
    Pingbacks are Off
    Refbacks are Off




    Sign Up Today!

    Ask our community of thousands of members your health questions, and learn from others experiences. Join the conversation!

    I want my free account

    All times are GMT -7. The time now is 03:18 AM.





    © 2022 MH Sub I, LLC dba Internet Brands. All rights reserved.
    Do not copy or redistribute in any form!