Forum Replies Created

  • Sharon

    Member
    September 14, 2023 at 5:03 pm in reply to: O2 and Essential Oils

    I am going on 2 years with mild PF. My acupuncturist who also has a Master’s in Chinese medicine recommended Green Mandarin spread over your collarbones. I go to him for my back, but when I told him about my PF, he put needles in the collarbone area, the lung nexus. And told me of a friend with another type of lung impairment, who used Green Mandarin, took a hike into a higher elevation & did better than her friends. I tried it for a while, but didn’t notice any difference. (I am also on Symbicort, but can’t tell if it’s doing anything, either.) He also recommended Natura 25 mg food-grown zinc & TRU Niagen Pro 500 for cellular energy & repair. I am seeing a new pulmonologist at the end of this month. My former one goes through the motions–6 months after prescribing Symbicort, he asked if I rinsed my mouth afterward… Luckily I had read the directions. His assistant gives me a breathing test & he says I’m still in the normal range. That’s it. I don’t notice any breathing impairment except if lifting something heavy or walking uphill. Scary, but not terrible exacerbations both times. I don’t do those things anymore.

  • Sharon

    Member
    July 10, 2022 at 1:17 am in reply to: Zinc in the Role of Lung Fibrosis

    After reading about zinc & PF, I asked my acupuncturist about it.  He did some research & recommended Natura 25 mg Food-Grown zinc, plus TRU Niagin Pro 500, which supports mitochondrial health.  He has Master degrees in acupuncture & Chinese herbal medicine, but does not disparage Western medicine.

    I had started to go to him for back pain & fatigue.  He has helped with both.  My shortness of breath upon exertion has also improved since I told him about PF, but that could also be due to  the pulmonologist prescribed Symbicort 80/4.5 with an extruder.  I have noticed that I sleep better, although I was never diagnosed with sleep apnea.

    I was diagnosed with mild stable IPF in the last 6 mos.  I won’t know if any of this has helped until I am tested again.  The problem was first spotted when I had a Medicare CT scan because I had been a heavy smoker.  A follow-up CT scan indicated possible PF.  A high resolution scan confirmed it.  I’m not eager to subject my body to more radiation, so it may be a year or so before I can report any test results.