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Allan Byron

Home Members Allan Byron
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@abyron888

Does anybody in the group had any experience or feed back on Wei institute mode of treatment? please share any experiences, etc you have, because i gave them a call for info, and the Soup ,A, B, etc will cost around $3,000.00. I am willing to try anything, but will appreciate any feedbacks. View
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Viewing 1 - 11 of 11 active members
  • Profile picture of Charlene Marshall
    Charlene Marshall
    Active 15 hours, 4 minutes ago
    - "I’m sharing the sad news that our amazing forum member, Chuck Harrison passed away late October. His wife Rose reached out to me to let me know, thanking all of us for supporting Chuck on this platform. May he […]"View
  • Profile picture of Steve Dragoo
    Steve Dragoo
    Active 2 days, 1 hour ago
    - "@lizmanualosteopath Hi Liz. Where did you get your Class 4 and how do you use it? Thanks, Steve"View
  • Profile picture of Nina Merendino
    Nina Merendino
    Active 4 days ago
    - "Nothing ! Seeing pulmonologist for testing next week."View
  • Profile picture of Mark Koziol
    Mark Koziol
    Active 3 weeks, 2 days ago
    - "Hello forum members, Tuesday is the day for my forum topic to be published. I’m going to go off script today and just ask one simple question: What does a good day look like for you? So many of us have e […]"View
  • Profile picture of Wendy Dirks
    Wendy Dirks
    Active 1 month ago
  • Profile picture of Dave Sabatelli
    Dave Sabatelli
    Active 1 month ago
  • Profile picture of Jojo
    Jojo
    Active 11 months, 1 week ago
    - "Can anybody advise what an exacerbation is with ipf."View
  • Profile picture of Doug Taylor
    Doug Taylor
    Active 1 year, 2 months ago
    - "I’m on OFEV (100mg/2 times/day) for IPF and Keytruda (200mg infusion every 3weeks) immunotherapy to preclude reoccurrence of melanoma. Both apparently cause shortness of breath which has gotten worse since s […]"View
  • Profile picture of Marsha
    Marsha
    Active 1 year, 10 months ago
    - "@wendyray @drandyhall @charlene-marshall Hi, Wendy! I just read your post about starting laser therapy and happily want to share my own laser therapy experience. First, please allow me to say that I […]"View
  • Profile picture of jaime L manriquez
    jaime L manriquez
    Active 1 year, 11 months ago
    - "@charlene-marshall Hello charlene , long time no post, Well my flegm ordeal has tapered down quite a bit I credited to prednisone for it , but only 5mg a day for a long time use. The bad news is that my IPF itis […]"View
  • Profile picture of Douglas k Freeman
    Douglas k Freeman
    Active 2 years, 2 months ago
    - "I was wondering about anyone that is doing or has done laser therapy for IPF? Can anyone tell me how the therapy has changed their disease for the better or no change? Also the cost as well as insurance coverage? […]"View
Viewing 1 - 11 of 11 active members
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Disclaimer

This site is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.

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