kayleesgrandma
New member
I need some help finding SeanDavis's post aboout the oregano oil, and it's uses. Also, where can I get it--health food stores? Thanks.
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SeanDavis and Oregano oil
- Thread starter kayleesgrandma
- Start date
Terri, Here's a few of the older ones. There are a ton more too. I did an advanced search on oregano oil. I wish SD was here to tell you himself- he was a wealth of info on supplemements.
<a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=23&threadid=6036&highlight_key=y&keyword1=oregano%20oil
">http://forums.cysticfibrosis.c...1=oregano%20oil
</a>
<a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=5&threadid=8370&highlight_key=y&keyword1=oregano%20oil
">http://forums.cysticfibrosis.c...1=oregano%20oil
</a>
<a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=5&threadid=7735&highlight_key=y&keyword1=oregano%20oil">http://forums.cysticfibrosis.c...keyword1=oregano%20oil</a>
<a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=23&threadid=6036&highlight_key=y&keyword1=oregano%20oil
">http://forums.cysticfibrosis.c...1=oregano%20oil
</a>
<a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=5&threadid=8370&highlight_key=y&keyword1=oregano%20oil
">http://forums.cysticfibrosis.c...1=oregano%20oil
</a>
<a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=5&threadid=7735&highlight_key=y&keyword1=oregano%20oil">http://forums.cysticfibrosis.c...keyword1=oregano%20oil</a>
kayleesgrandma
New member
Thanks Jane, I made copies of this stuff so can read later. I appreciate it.
kayleesgrandma
New member
Well, DUH--dum dum me figured out to go to search topic and I struck pay dirt! Went all the way back to 2004. I used tons of paper from here at work copying so I could read at home. Now my question is--where is the SeanDavis of the oregano oil? Not the one we have seen here recently, but the kind, witty, serious, and oh so informative gentleman of the posts. That's the SeanDavis that I first met when I came here. I want him back--<i>that</i> SeanDavis! I think we're all eternally grateful for your contribution about it use and benefit to all of us. Thanks SD.
teknogeek1300
New member
Long story short, Sean is no longer with us....
<a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=17&threadid=9113&enterthread=y">http://forums.cysticfibrosis.c...did=9113&enterthread=y</a>
<a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=17&threadid=9113&enterthread=y">http://forums.cysticfibrosis.c...did=9113&enterthread=y</a>
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>teknogeek1300</b></i>
Long story short, Sean is no longer with us....
</end quote></div>
As in isnt/cant/wont log on anymore.....I dont know if ANYONE has actually spoken with him to find out the truth of his absence!
Long story short, Sean is no longer with us....
</end quote></div>
As in isnt/cant/wont log on anymore.....I dont know if ANYONE has actually spoken with him to find out the truth of his absence!
C
Cutecurlz
Guest
I know you can buy Oil of Oregano at any health food store...that's where I got mine. FYI, it's exspensive. The higher the price the better it works. I payed $60 buckx for a 6 ounce bottle I think that's the right size.
Davidkramer
New member
Hello,<br>
First, I must know if we are talking about Sean Davis who, the last
time I saw him lived in Bradonton Florida? Sean formerly of Akron
Ohio, born in Sao paulo Brazil?<br>
If so this is my cousin and I would like very much to contact
him.<br>
My grand son was recently diagnosed with Immotile Cilia Syndrome A
cousin to CF.<br>
If anyone can help contact Sean, Please Do.<br>
dkramer13@tampabay.rr.com<br>
<br>
Thanks,<br>
David Kramer<br>
Homosassa, Fl.
First, I must know if we are talking about Sean Davis who, the last
time I saw him lived in Bradonton Florida? Sean formerly of Akron
Ohio, born in Sao paulo Brazil?<br>
If so this is my cousin and I would like very much to contact
him.<br>
My grand son was recently diagnosed with Immotile Cilia Syndrome A
cousin to CF.<br>
If anyone can help contact Sean, Please Do.<br>
dkramer13@tampabay.rr.com<br>
<br>
Thanks,<br>
David Kramer<br>
Homosassa, Fl.
Davidkramer
New member
What are oo treatments?<br>
I haven't seen him in something like 19 years...
I haven't seen him in something like 19 years...
Davidkramer
New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>amy</b></i> David, as you can see by
the threads, we can't get a hold of him.</end quote></div><br>
<br>
I just read his Blogs, sounds like Sean has grown to be quite the
caricature. I too hope he is well, and I hope he is as smart as
everyone says he is about CF, and I hope he is generous with his
knowledge.
the threads, we can't get a hold of him.</end quote></div><br>
<br>
I just read his Blogs, sounds like Sean has grown to be quite the
caricature. I too hope he is well, and I hope he is as smart as
everyone says he is about CF, and I hope he is generous with his
knowledge.
Davidkramer
New member
Thank You Amy.
Davidkramer
New member
My hope is that someone knows Sean on a level that would
precipitate their having his e-mail address and that they pass
along my e-mail address to him.
precipitate their having his e-mail address and that they pass
along my e-mail address to him.
kayleesgrandma
New member
Thanks everyone, just thought I'd check out his theory about OO. I think Kaylee's too young yet, but was planning for the future.
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>kayleesgrandma</b></i>
Thanks everyone, just thought I'd check out his theory about OO. I think Kaylee's too young yet, but was planning for the future.</end quote></div>
I dunno, for me it helped a lot.
From 2003-2005 my fev1 went from 77 to 65 to 55...for no paticular reason. My doctors were kinda distressed, but wasn't really sure what was going on. I too was a little worried...but at the time i didn't culture pseudo, so options of treating were limited to taking oral ABX when i got an infection, which was rare. This rational thinking drove me nuts, cause my lung function was dropping so much and the doctors seemingly didn't care
I think it was December of last year that i tried it, and within 3 months my fev1 went to 87% and my fev25 was 103. I was smiling so much. My doctors were amazed. I didn't tell them the at first, cause i wanted to have another test done before i could confirm the results
I have another clinic due soon, so i will let you guys know what happens. You know, as Sean has stated so many times before, the doctors are so focused on their methods of treatement that they really don't investigate other alternatives. Hence the amazing part of this site. Despite the disputes, this place is pretty amazing.
You know, inhaling it might not be for everyone...cause it is harsh, however, taken orally, i don't see the problems with it. You know, we are living with a terminal illness, so we have to make dicisions about our health and wiegh the negative and poitive aspects of this. If you're in perfect health, then perhaps you don't need it. If your lung function is going down, then why not give it a try, and many other of the alternative therapies around...
In the end, this is our health, our lives...and we make the decisions. Doctors are amazing for certain things, but it's still our duty to take care of ourselves..
Thanks everyone, just thought I'd check out his theory about OO. I think Kaylee's too young yet, but was planning for the future.</end quote></div>
I dunno, for me it helped a lot.
From 2003-2005 my fev1 went from 77 to 65 to 55...for no paticular reason. My doctors were kinda distressed, but wasn't really sure what was going on. I too was a little worried...but at the time i didn't culture pseudo, so options of treating were limited to taking oral ABX when i got an infection, which was rare. This rational thinking drove me nuts, cause my lung function was dropping so much and the doctors seemingly didn't care
I think it was December of last year that i tried it, and within 3 months my fev1 went to 87% and my fev25 was 103. I was smiling so much. My doctors were amazed. I didn't tell them the at first, cause i wanted to have another test done before i could confirm the results
I have another clinic due soon, so i will let you guys know what happens. You know, as Sean has stated so many times before, the doctors are so focused on their methods of treatement that they really don't investigate other alternatives. Hence the amazing part of this site. Despite the disputes, this place is pretty amazing.
You know, inhaling it might not be for everyone...cause it is harsh, however, taken orally, i don't see the problems with it. You know, we are living with a terminal illness, so we have to make dicisions about our health and wiegh the negative and poitive aspects of this. If you're in perfect health, then perhaps you don't need it. If your lung function is going down, then why not give it a try, and many other of the alternative therapies around...
In the end, this is our health, our lives...and we make the decisions. Doctors are amazing for certain things, but it's still our duty to take care of ourselves..