pulmonary function test

[Eva Holloway]

Had the best pulmonary function test yet. My doctor asked me to write down what medication and supplements I take because he has a few patients with interstitial pulmonary fibrosis and they are not doing as well as I have. He wants to check the AP out to see if he can help others with this health issue. He wants me to do a pulmonary function test for a little while longer to make sure I am staying the course.
Eva 😀 😀 😀 😀

Eva Holloway

[maz.aust]

HI EVA,

WHAT FANTASTIC NEWS, you couldn’t have asked for a better result !!! WHOO HOO !!!!!!!!

& just great that your doctor is open to looking at AP,

🙂 🙂 🙂 🙂 🙂 🙂 🙂 🙂 🙂

Dec07: Diagnosed PRA, (CTD; Fibromyalgia; suspected Lyme):
Mar08: Diet to heal gut/bolster immune system (no gluten, dairy, sulphites or sugar)

Jan 2018: ABX Mon/Wed/Fri (started AP 2008)
1/2 x 150mg Roxithromycin(Biasig), 1/2 x 150mg Clarithromycin (Klacid),
1/2 x Fungillin, 1 x 250mg Cephalexin (Keflex)

All off days Probiotics

[lynnie_sydney]

Had the best pulmonary function test yet.

EVAAAAAAAAAA! Your post has made my day…..wow the news just keeps getting better and better. So happy for you, you’ve worked so hard for this. I’m just sorry we dont have the ‘dude’ icon over here. 😀 😀 😀 😀 😀 😀 😀 Lynnie

Be well! Lynnie

Palindromic RA 30 yrs (Chronic Lyme?)
Mino 2003-2008 100mg MWF - can no longer tolerate any tetracyclines
rotating abx protocol now. From Sep 2018 MWF - a.m. Augmentin Duo 440mg + 150mg Biaxsig (roxithromycin). p.m. Cefaclor (375mg) + Klacid 125mg + LDN 3mg + Annual Clindy IV's
Diet: no gluten, dairy, sulphites, low salicylates
Supps: 600mg N-AC BID, 1000mg Vit C, P5P 40mg, zinc picolinate 60mg, Lithium orotate 20mg, Magnesium Oil, Bio-identical hormones (DHEA + Prog + Estrog)

[Eva Holloway]

Lynnie and Maz.aust
I think I am finally getting the pulmonary on the right page, he was asking all kinds of questions, I did give him the book the new arthritis breakthrough, but I don’t think he has read all of it yet, LOL 😆
I am so glad at least my lungs are good now, I think the rest will slowly follow. I keep thinking just another year maybe but I wish I would be lots better by middle of September since our choir is going for two weeks to Germany. I can walk better too.
Thank you for your encouragement at all times.
Eva 🙂

Eva Holloway

[Parisa]

Eva,

That’s great news. You’ve not only helped yourself but hopefully your doctor will change some of his protocols to help more of his patients.

[Krys]

Eva, what lovely news!!!! And more people will be getting better thanks to you! Wow!!! Go, Eva, GO!!!!

[Maz]

Eva, I am just so thrilled for you…you just keep going from strength to strength and you continue to be an inspiration to all here. Thank you for sharing your uplifting updates. You made my day, too! 😀 Hey…and if we can have one more physician convert, all the better!

[hopefulmama]

Eva,

I am more thrilled than I can say by your news. Congratulations!!! It’s so wonderful that you’ve made so much improvement thanks to your hard work, faith and dedication… you are a real inspiration and I hope other RBF members who suffer from pulmonary problems will find your post and realize that there is HOPE and they can truly recover their lung function. Just reading about your results brought tears to my eyes… happy, joyful tears!

Take care and keep getting better every day 🙂

Warmly,
Andrea

[nspiker]

Yippee Eva…..

What wonderful news. 😀 😀 😀 😀 😀 😀 😀 😀 😀 😀 😀 😀 😀 You really are an inspiration and an example for all of us that attitude and effort prevail!

How refreshing that your doctor actually gives credit to YOU and your treatment, and is willing to learn about AP to help other patients.
nancy

[Trudi]

@Eva Holloway wrote:

Had the best pulmonary function test yet. My doctor asked me to write down what medication and supplements I take because he has a few patients with interstitial pulmonary fibrosis and they are not doing as well as I have. He wants to check the AP out to see if he can help others with this health issue.

Eva–
Your results and your doctor’s response is AMAZING!! What an uplifting post. Keep up this wonderful route to recovery!!

Take care,
Trudi

Lyme/RA; AP 4/2008 off and on to 3/2010; past use of quinolones may be the cause of my current problems, (including wheelchair use); all supplements (which can aggravate the condition) were discontinued on 10/14/2012. Am now treating for the homozygous MTHFR 1298 mutation. Off of all pain meds since Spring '14 (was on them for years--doctor is amazed--me too). Back on pain med 1/2017. Reinfected? Frozen shoulder?

[dianne-sunshinecoast]

hi eva, i have only just met you, but from the start i have been inspired and encouraged by your posts 🙂 .i am so very very happy for you and your good news, continued good healthto you always 🙂 🙂 🙂 ….kind regards ..di. 🙂

[Valsmum]

Congrats Eva !!
I’m so very happy for you and it’s so nice to hear about a Dr. that acknowledges your treatment and might help others with this information. Thanks for sharing.
Take care,
Sheri

[Lynne G.SD]

Eva,I am so happy for you.Did you save the article that was posted here about Zith and lung fibrosis?Printing that for your doc. might help him.If you don’t have it I think that I do somewhere in some file.
Lynne

[Eva Holloway]

Lynne G.
would you please forward the info for me. He is still interested in the Minocin and Biaxin combo with the supplements I use. He is specially interested in NAC. He read up on it, so hopefully it will be part of what he will give to his patients if they have a n issue.
I made blueberry jam today and will make strawberry jam tomorrow. I have been very busy, but I still will take rests when I need it.
Eva 🙂

Eva Holloway

[Lynne G.SD]

Hi Eva; We have already proved that Zith works for humans since we are the Guinea pigs and know it helps. hehehe

http://www.ncbi.nlm.nih.gov/pubmed/20874225

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