I have MAC Does anyone else? and is it really bad to have??

D

Daisylane

New member
Hi Guys, I am brand new to this site. I just joined today, and very happy that I did. I love all the information from others and support. I Have just recently been diagnosed with MAC. I already have CF, MRSA and CFRD. I have no clue what MAC is and is it super dangerous to have? What do you guys notice who also have it that's different with your day to day routine if any?

I am a female 26 w/ CF / MRSA / CFRD /MAC...have a BF and living life to the fullest <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
D

Daisylane

New member
Hi Guys, I am brand new to this site. I just joined today, and very happy that I did. I love all the information from others and support. I Have just recently been diagnosed with MAC. I already have CF, MRSA and CFRD. I have no clue what MAC is and is it super dangerous to have? What do you guys notice who also have it that's different with your day to day routine if any?

I am a female 26 w/ CF / MRSA / CFRD /MAC...have a BF and living life to the fullest <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
D

Daisylane

New member
Hi Guys, I am brand new to this site. I just joined today, and very happy that I did. I love all the information from others and support. I Have just recently been diagnosed with MAC. I already have CF, MRSA and CFRD. I have no clue what MAC is and is it super dangerous to have? What do you guys notice who also have it that's different with your day to day routine if any?
<br />
<br />I am a female 26 w/ CF / MRSA / CFRD /MAC...have a BF and living life to the fullest <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
P

Printer

Active member
Hi:
<br />
<br />MAC stands for Mycobacterium Avium Complex. For more info you can Google it.
<br />
<br />Bill
 
H

hmw

New member
Hi and welcome. <img src="i/expressions/face-icon-small-smile.gif" border="0"> If you post again in the Adults forum and ask about it, you will find there are multiple others that deal with this and I am sure they will be happy to share their experiences (treatments, how it has affected the course of their cf, etc.) I don't have any personal experience with it (it's my daughter with CF) but wanted to let you know that there are many who are knowledgeable here about this that will be able to help. <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
H

hmw

New member
Hi and welcome. <img src="i/expressions/face-icon-small-smile.gif" border="0"> If you post again in the Adults forum and ask about it, you will find there are multiple others that deal with this and I am sure they will be happy to share their experiences (treatments, how it has affected the course of their cf, etc.) I don't have any personal experience with it (it's my daughter with CF) but wanted to let you know that there are many who are knowledgeable here about this that will be able to help. <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
H

hmw

New member
Hi and welcome. <img src="i/expressions/face-icon-small-smile.gif" border="0"> If you post again in the Adults forum and ask about it, you will find there are multiple others that deal with this and I am sure they will be happy to share their experiences (treatments, how it has affected the course of their cf, etc.) I don't have any personal experience with it (it's my daughter with CF) but wanted to let you know that there are many who are knowledgeable here about this that will be able to help. <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
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