Is no one interested in Mucolyxir, A powerful new treatment? How many are using it?

P

PeterC

New member
I am very excited about the possibilities of this new easy to use aide in combating lung congestion.

If it proves to be as effective as some have stated here and on other sites it could be a major step forward in dealing with lung congestion and preventing infections.

For those that are using it, what are your experiences?

Sincerely:

PeterC 58/cf
 
P

PeterC

New member
I am very excited about the possibilities of this new easy to use aide in combating lung congestion.

If it proves to be as effective as some have stated here and on other sites it could be a major step forward in dealing with lung congestion and preventing infections.

For those that are using it, what are your experiences?

Sincerely:

PeterC 58/cf
 
P

PeterC

New member
I am very excited about the possibilities of this new easy to use aide in combating lung congestion.

If it proves to be as effective as some have stated here and on other sites it could be a major step forward in dealing with lung congestion and preventing infections.

For those that are using it, what are your experiences?

Sincerely:

PeterC 58/cf
 
P

PeterC

New member
So where are all you folks using this stuff?

Is there no interest in it and if not why not?

PeterC 58/cf
 
P

PeterC

New member
So where are all you folks using this stuff?

Is there no interest in it and if not why not?

PeterC 58/cf
 
P

PeterC

New member
So where are all you folks using this stuff?

Is there no interest in it and if not why not?

PeterC 58/cf
 
P

princessjdc

New member
Im not using it Peter mainly cause I dont know about it and I havent looked into either but if you have some good useful info to share with me Ill be glad to look it over and maybe give it a shot if doc approves of course, are you currently on it? Im guessing not but thought I would ask. Do you know if its nebbed or if its an inhaler or a pill, cause if its another neb then Im not sure if I want to miss with getting it, also does it raise PFTS, cause if thats a YES then I will diffanatley look into it and most likely tell my doc. Sorry no one on here has posted about it yet, hopefully they will though.
 
P

princessjdc

New member
Im not using it Peter mainly cause I dont know about it and I havent looked into either but if you have some good useful info to share with me Ill be glad to look it over and maybe give it a shot if doc approves of course, are you currently on it? Im guessing not but thought I would ask. Do you know if its nebbed or if its an inhaler or a pill, cause if its another neb then Im not sure if I want to miss with getting it, also does it raise PFTS, cause if thats a YES then I will diffanatley look into it and most likely tell my doc. Sorry no one on here has posted about it yet, hopefully they will though.
 
P

princessjdc

New member
Im not using it Peter mainly cause I dont know about it and I havent looked into either but if you have some good useful info to share with me Ill be glad to look it over and maybe give it a shot if doc approves of course, are you currently on it? Im guessing not but thought I would ask. Do you know if its nebbed or if its an inhaler or a pill, cause if its another neb then Im not sure if I want to miss with getting it, also does it raise PFTS, cause if thats a YES then I will diffanatley look into it and most likely tell my doc. Sorry no one on here has posted about it yet, hopefully they will though.
 
K

KrazyKat

New member
I'm interested but i suspect it may be too soon for those using it to notice any real results, hence they're not posting. I would imagine, like any other therapy it might take up to three months to show any real results and what i want to see before i try it myself is an increase in FEV1, which will mean whoever is currently testing it, needs to have a clinic appointment before the results will be clear.
It isn't nebbed, from memory it is drops under the tongue, much like oregano oil was to start with.
 
K

KrazyKat

New member
I'm interested but i suspect it may be too soon for those using it to notice any real results, hence they're not posting. I would imagine, like any other therapy it might take up to three months to show any real results and what i want to see before i try it myself is an increase in FEV1, which will mean whoever is currently testing it, needs to have a clinic appointment before the results will be clear.
It isn't nebbed, from memory it is drops under the tongue, much like oregano oil was to start with.
 
K

KrazyKat

New member
I'm interested but i suspect it may be too soon for those using it to notice any real results, hence they're not posting. I would imagine, like any other therapy it might take up to three months to show any real results and what i want to see before i try it myself is an increase in FEV1, which will mean whoever is currently testing it, needs to have a clinic appointment before the results will be clear.
It isn't nebbed, from memory it is drops under the tongue, much like oregano oil was to start with.
 
M

moxie1

Guest
Peter,

I guess you didn't see my other post.

I was disappointed at my check-up, because although I've been feeling great, my pfts weren't much better. My FEV1 was up 1% and the small airways (FEV25-75%) were up 4%.

I think it is too soon to say. This weekend I hadn't been feeling as good. I felt like I had stuff down there that wasn't coming up. Everytime I coughed, though, it was super thin.

Today was better--got alot up during my vest.

Bottom line--my phlegm is so much thinner and I will keep on the mucolyxir for another few months at least. I want to give it a chance to improve my pfts if it is going to.
 
M

moxie1

Guest
Peter,

I guess you didn't see my other post.

I was disappointed at my check-up, because although I've been feeling great, my pfts weren't much better. My FEV1 was up 1% and the small airways (FEV25-75%) were up 4%.

I think it is too soon to say. This weekend I hadn't been feeling as good. I felt like I had stuff down there that wasn't coming up. Everytime I coughed, though, it was super thin.

Today was better--got alot up during my vest.

Bottom line--my phlegm is so much thinner and I will keep on the mucolyxir for another few months at least. I want to give it a chance to improve my pfts if it is going to.
 
M

moxie1

Guest
Peter,

I guess you didn't see my other post.

I was disappointed at my check-up, because although I've been feeling great, my pfts weren't much better. My FEV1 was up 1% and the small airways (FEV25-75%) were up 4%.

I think it is too soon to say. This weekend I hadn't been feeling as good. I felt like I had stuff down there that wasn't coming up. Everytime I coughed, though, it was super thin.

Today was better--got alot up during my vest.

Bottom line--my phlegm is so much thinner and I will keep on the mucolyxir for another few months at least. I want to give it a chance to improve my pfts if it is going to.
 
C

cf4life

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>PeterC</b></i>

So where are all you folks using this stuff?



Is there no interest in it and if not why not?

PeterC 58/cf</end quote></div>


Have you tried it? Why not?
 
C

cf4life

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>PeterC</b></i>

So where are all you folks using this stuff?



Is there no interest in it and if not why not?

PeterC 58/cf</end quote></div>


Have you tried it? Why not?
 
C

cf4life

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>PeterC</b></i>

So where are all you folks using this stuff?



Is there no interest in it and if not why not?

PeterC 58/cf</end quote></div>


Have you tried it? Why not?
 
D

dasjsmum

New member
I think you should give it a go too Peter. It's not very expensive, and the protocol is one drop every 15 mins for first hour, and one drop every hour for the first day. After that it is one drop four times daily I think.

We have some, and I have my older son trying it...he's been on it only since Saturday, but thinks his sputum is thinner and easier to cough up. It is pretty hard to know whether it's placebo effect though. He did go to the clinic yesterday, but I forgot to ask him how it went...he had just done a course of nebbed a/bs, so probably doesnt show much evidence.

One of the studies I was reading on it was done over three months, so I think we'll have to give it a bit longer. Here's a link to it (hope it works), and the other is where myself and others gotten mucolixer from.


<a target=_blank class=ftalternatingbarlinklarge href="http://www.ana-jana.org/members/journals/JANAVol_91.pdf
">http://www.ana-jana.org/member...urnals/JANAVol_91.pdf
</a>
<a target=_blank class=ftalternatingbarlinklarge href="http://www.springboard4health.com/store/more_arg_mucolyxir.html">http://www.springboard4health....ore_arg_mucolyxir.html</a>
 
D

dasjsmum

New member
I think you should give it a go too Peter. It's not very expensive, and the protocol is one drop every 15 mins for first hour, and one drop every hour for the first day. After that it is one drop four times daily I think.

We have some, and I have my older son trying it...he's been on it only since Saturday, but thinks his sputum is thinner and easier to cough up. It is pretty hard to know whether it's placebo effect though. He did go to the clinic yesterday, but I forgot to ask him how it went...he had just done a course of nebbed a/bs, so probably doesnt show much evidence.

One of the studies I was reading on it was done over three months, so I think we'll have to give it a bit longer. Here's a link to it (hope it works), and the other is where myself and others gotten mucolixer from.


<a target=_blank class=ftalternatingbarlinklarge href="http://www.ana-jana.org/members/journals/JANAVol_91.pdf
">http://www.ana-jana.org/member...urnals/JANAVol_91.pdf
</a>
<a target=_blank class=ftalternatingbarlinklarge href="http://www.springboard4health.com/store/more_arg_mucolyxir.html">http://www.springboard4health....ore_arg_mucolyxir.html</a>
 
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