New era for ME/CFS research as top cytokine study attracts media headlines
The immune systems of patients who have recently developed ME/CFS look markedly different from those who have been ill for much longer, according to a major new study from Drs. Ian Lipkin and Mady Hornig at Columbia University. This shift in immune function hadn’t been seen before.
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Asthma, who else has it?

Discussion in 'Autonomic, Cardiovascular, and Respiratory' started by xks201, Oct 18, 2012.

  1. xks201

    xks201 Senior Member

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    Just curious.
     
  2. justy

    justy Senior Member

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    Diagnosed with exercise induced Asthma at 6. Never had attacks though - but have had bronchitis and lung infections regularly between that age and now (43) Now dealing with pulmonary fibrosis and my consultant thinks i dont have asthma after all - he offered to test for this with an exercise stress test - which i am not well enough, M.E wise to perform.

    (What a surprise, nothing straightforward here!)
    All the best, Justy.
     
  3. silicon

    silicon Senior Member

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    I do, since childhood, well before ME/CFS. It was brought on by allergies and sometimes aerobic exercise/sports. I do regret being on anti-asthma stimulants for many years, back in the day.
     
    justy likes this.
  4. nanonug

    nanonug Senior Member

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    If ME/CFS is indeed what I think it is (MCAS), then asthma/shortness of breath almost follows logically.
     
  5. beaverfury

    beaverfury beaverfury

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    West Australia
    I was an asthmatic as a child. Up until my teens.

    Started taking deprenyl and got a reccurence of asthma which i havent had in ages. Maybe a temporary issue, but have ceased taking it anyway.
     
  6. beaverfury

    beaverfury beaverfury

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    Nah, i'm back on it. Asthma symptoms have resolved. Yip
     
  7. Stretched

    Stretched

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    Yes, shortly after definitively having 'something' causing chest pain and congestion, i.e. before CFS identified,
    I used spray Ventolin, some preventative powder spray(?), and Theophyillin for ~ 2 years. I took these along with a lot of Entrex (guaifenasin) under the theory (by Endocrinologist) this would break up the mucosal congestion and the sprays would dialate the Aveoli so I'd get back to 'normal' and be without chest pain, sic around the rib cage.

    'Normal' didn't come and my CFS paralleled press reports, and I had been to Incline Village. So I dropped the Asthma protocol (to keep rx's at a reduced level) and used Medrol packs (prednisone) ~ 3-4 times a year along with
    other meds for symptoms.

    FWIW, the pred treatment helped the most in my not worrying about Asthma. This was 25 years ago and I'm considering revisiting this protocol even if it's only palliative. For me chest pains around the rib cage and back have returned as one of the most identifying 'flare' features of my ME, which waxes and wanes; and I mean the pain can really be limiting.

    I hope this bit of shared history helps along the lines you were exploring.
     

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