Do you regularly use any of these "Asthma" meds?

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crickit715

New member
Do you regularly use any of these

quoting from above: ((I do not think being African American, white, blue , whatever has anything to do with CF, either you have it or you don't, right))

FYI: actually some mutations are specific to certain nationalites. when they performed my daughters dna test they did specific testing for mutations known to populate the hispanic/latino cf individuals because her father is from central america. there are specific mutations they check for in the african american population as well. <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
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crickit715

New member
Do you regularly use any of these

quoting from above: ((I do not think being African American, white, blue , whatever has anything to do with CF, either you have it or you don't, right))
<br />
<br />FYI: actually some mutations are specific to certain nationalites. when they performed my daughters dna test they did specific testing for mutations known to populate the hispanic/latino cf individuals because her father is from central america. there are specific mutations they check for in the african american population as well. <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
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crickit715

New member
Do you regularly use any of these

hhmmm... im pretty sure they dont..because some of them dont start with D...they start with G or R. but i could be wrong!
 
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crickit715

New member
Do you regularly use any of these

hhmmm... im pretty sure they dont..because some of them dont start with D...they start with G or R. but i could be wrong!
 
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crickit715

New member
Do you regularly use any of these

hhmmm... im pretty sure they dont..because some of them dont start with D...they start with G or R. but i could be wrong!
 
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MaksNana

New member
Do you regularly use any of these

Yes Ricki,
I am fully aware of different nationalities and mutations.
I think Bink can answer questions about Herself.
I asked what were her gene mutations, which it's obvious she does not know. I didn't feel the need to write a book about CF genes, to ask someone if they would share their mutations.Very simple!

Bink it is good that you cough out the mucous. Are you PI or PS?
I would love to know more about you from you.
Thank you, karla<img src="i/expressions/face-icon-small-wink.gif" border="0">
 
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MaksNana

New member
Do you regularly use any of these

Yes Ricki,
I am fully aware of different nationalities and mutations.
I think Bink can answer questions about Herself.
I asked what were her gene mutations, which it's obvious she does not know. I didn't feel the need to write a book about CF genes, to ask someone if they would share their mutations.Very simple!

Bink it is good that you cough out the mucous. Are you PI or PS?
I would love to know more about you from you.
Thank you, karla<img src="i/expressions/face-icon-small-wink.gif" border="0">
 
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MaksNana

New member
Do you regularly use any of these

Yes Ricki,
<br />I am fully aware of different nationalities and mutations.
<br />I think Bink can answer questions about Herself.
<br />I asked what were her gene mutations, which it's obvious she does not know. I didn't feel the need to write a book about CF genes, to ask someone if they would share their mutations.Very simple!
<br />
<br />Bink it is good that you cough out the mucous. Are you PI or PS?
<br />I would love to know more about you from you.
<br />Thank you, karla<img src="i/expressions/face-icon-small-wink.gif" border="0">
 
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cmorgan

New member
Do you regularly use any of these

uhm. 1st off. I am a he. Also, I was aware that crikit715 and myself were BOTH correct about the correlation between ethnicity and CF. There does seem to be a connection of some sort. The question was not the connection but rather asking what the nature of that connection is and what that may do(if anything) to help the ACTUAL CF researchers create a solution that benefits us all. Furthermore, being rude or short with people is completely unnecessary in a conversation about CF. Let's be real..you are not going to personally make any significant findings or revelations about CF from merely learning my mutation or anyone elses.
 
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cmorgan

New member
Do you regularly use any of these

uhm. 1st off. I am a he. Also, I was aware that crikit715 and myself were BOTH correct about the correlation between ethnicity and CF. There does seem to be a connection of some sort. The question was not the connection but rather asking what the nature of that connection is and what that may do(if anything) to help the ACTUAL CF researchers create a solution that benefits us all. Furthermore, being rude or short with people is completely unnecessary in a conversation about CF. Let's be real..you are not going to personally make any significant findings or revelations about CF from merely learning my mutation or anyone elses.
 
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cmorgan

New member
Do you regularly use any of these

uhm. 1st off. I am a he. Also, I was aware that crikit715 and myself were BOTH correct about the correlation between ethnicity and CF. There does seem to be a connection of some sort. The question was not the connection but rather asking what the nature of that connection is and what that may do(if anything) to help the ACTUAL CF researchers create a solution that benefits us all. Furthermore, being rude or short with people is completely unnecessary in a conversation about CF. Let's be real..you are not going to personally make any significant findings or revelations about CF from merely learning my mutation or anyone elses.
 
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MaksNana

New member
WOW,,, Mr. He,
No one was getting short. My questions were not to get you in a hissy,,,,,, gezzzzzzzzzzzz. If you go back and read what I wrote to YOU, not ricky, than maybe you will understand.
I am very iterested in everyone's mutations, rather you feel that they will make any significant findings or not.

Some of the new trials are for only certain CF mutations, so ,I think they might make some difference.

Plus I was interested in the Advair question , wondering if you had problems with it, Mak is on it , and she is still to young to know if one of her million meds may be effecting her wrong.


There are certainly more important and significant things going on in people's lives right now than to argue with someone over something so petty, and obviosly I am sure why this is going on. So I would appreciate no more answers if you are going to get upset if asked. All you had to say is, 'I don't know',but , wow!

I honestly wish you the best,,,,,,and sorry if I affended you, very sorry......... Karla <img src="i/expressions/wine.gif" border="0">
 
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MaksNana

New member
WOW,,, Mr. He,
No one was getting short. My questions were not to get you in a hissy,,,,,, gezzzzzzzzzzzz. If you go back and read what I wrote to YOU, not ricky, than maybe you will understand.
I am very iterested in everyone's mutations, rather you feel that they will make any significant findings or not.

Some of the new trials are for only certain CF mutations, so ,I think they might make some difference.

Plus I was interested in the Advair question , wondering if you had problems with it, Mak is on it , and she is still to young to know if one of her million meds may be effecting her wrong.


There are certainly more important and significant things going on in people's lives right now than to argue with someone over something so petty, and obviosly I am sure why this is going on. So I would appreciate no more answers if you are going to get upset if asked. All you had to say is, 'I don't know',but , wow!

I honestly wish you the best,,,,,,and sorry if I affended you, very sorry......... Karla <img src="i/expressions/wine.gif" border="0">
 
M

MaksNana

New member
WOW,,, Mr. He,
<br />No one was getting short. My questions were not to get you in a hissy,,,,,, gezzzzzzzzzzzz. If you go back and read what I wrote to YOU, not ricky, than maybe you will understand.
<br />I am very iterested in everyone's mutations, rather you feel that they will make any significant findings or not.
<br />
<br />Some of the new trials are for only certain CF mutations, so ,I think they might make some difference.
<br />
<br />Plus I was interested in the Advair question , wondering if you had problems with it, Mak is on it , and she is still to young to know if one of her million meds may be effecting her wrong.
<br />
<br />
<br />There are certainly more important and significant things going on in people's lives right now than to argue with someone over something so petty, and obviosly I am sure why this is going on. So I would appreciate no more answers if you are going to get upset if asked. All you had to say is, 'I don't know',but , wow!
<br />
<br />I honestly wish you the best,,,,,,and sorry if I affended you, very sorry......... Karla <img src="i/expressions/wine.gif" border="0">
 
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beleache

New member
I have been using Advai 250/50 for a few years now.. We tried taking me off but I ended up in the hosp for a week on IV Steroids..

<img src="i/expressions/heart.gif" border="0"> joni
 
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beleache

New member
I have been using Advai 250/50 for a few years now.. We tried taking me off but I ended up in the hosp for a week on IV Steroids..

<img src="i/expressions/heart.gif" border="0"> joni
 
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beleache

New member
I have been using Advai 250/50 for a few years now.. We tried taking me off but I ended up in the hosp for a week on IV Steroids..
<br />
<br /><img src="i/expressions/heart.gif" border="0"> joni
 
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