How many have had the Big 3 cure, then relapsed?

Posted by healthybon @healthybon, Jul 19, 2023

Hi everyone,
I would like to know how many people took the big three THERAPY, then their tests showed that Mac was gone, and then it returned.

I would appreciate any input on this. Thanks Bon

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@sue22

Hi Tina
Very sorry that you are having more coughing. Are you monitored by a local doctor or NJH during this period? How often do you have sputum cultures . I hope to finish treatment soon for MAC and wondered what the protocol for follow up may be. Thank you if you want to share.
Susan

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I've known for a year or so that my MAC came back. I went to NJH in April and they confirmed but said my CT scan had improved. I am now going to my local pulmonologist that NJ said was excellent. He diagnosed me with everything but had been pressuring me to go back on the meds. I wanted NJ opinion. I was supposed to go back next month but have cancelled. They also diagnosed with me CF so I'm off to a CF clinic one of these days. I'm really just overwhelmed. My sputum cultures breeding as I type. My local doctor insists on frequent cultures.

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@tinaesims

I try to stay active. I still golf and go to exercise class. I did golf in a big outing yesterday and today I'm resting. I used to be able to go, go, go!

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I played golf on Wednesday, fishing on boat on Thursday, today I am resting at work i my office chair. I was diagnosed 5 years ago with MAC/cavitary , currently I am treated for fungal infection that sat in a year ago.

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@rstel7272

I played golf on Wednesday, fishing on boat on Thursday, today I am resting at work i my office chair. I was diagnosed 5 years ago with MAC/cavitary , currently I am treated for fungal infection that sat in a year ago.

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Rick..what do they do for the cavity, if anything? What are the symptoms? Bon

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@sueinmn

Oh, Tina, I'm sorry to hear that - what are you doing to try to get healthy? Every year around this time I get a little anxious and hyper-alert to every cough and wheeze as I await a followup CT and whether I need a culture. I am 43 months out from stopping the antibiotics while still positive, but my lungs have been stable🤞🤞Sue

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Hi Sue,
I guess I’m not as brave as a lot of our fellow bloggers. I know I have written to you many times. You seem knowledgeable and strong.
I’m struggling Sue, really badly. Mentally. Since I saw Dr Swenson the other day. He said he’s concerned…..

Maybe you can share with me how you deal with all of this.. I just got Diagnosis this past year. Dr Swenson wants to start me on Azithromycin and ethambutol, slowly because I’m so sensitive. I guess he feels the MAC needs to be treated so it doesn’t turn into cavities etc. I am so terrified….I can hardly function. My reaction to antibiotics is not good…I get so sick. The thought of being on them for such a long time freaks me out. It’s like I’m boxed in a corner.
My entire rib cage hurts and he feels the infection and inflammation is exacerbating my costochondritis. When I wake up in the morning and open my eyes, I am immobilized with fear at the prospect of taking that medicine for such a long time….., and/or what will happen to me if I don’t. I pray……
As soon as he speaks to my Opthomologist he wants me to start first with the azithromycin three times a week, then add the ethambutol. He wants my eyes checked every three months.

He said if it makes you too sick you will stop. So then I could develop cavities and not be able to breathe. I’m so discouraged and very scared Sue..

Sue, how did the meds affect YOU.
Any suggestions? Bon

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@healthybon

Rick..what do they do for the cavity, if anything? What are the symptoms? Bon

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While treating the other diseases with the big 3, etc, the cavity may close by itself. I am not so lucky, I have scar tissue in and around the lung. Surgery is an option to remove the bleb, lobe or entire lung.

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@healthybon

Hi Sue,
I guess I’m not as brave as a lot of our fellow bloggers. I know I have written to you many times. You seem knowledgeable and strong.
I’m struggling Sue, really badly. Mentally. Since I saw Dr Swenson the other day. He said he’s concerned…..

Maybe you can share with me how you deal with all of this.. I just got Diagnosis this past year. Dr Swenson wants to start me on Azithromycin and ethambutol, slowly because I’m so sensitive. I guess he feels the MAC needs to be treated so it doesn’t turn into cavities etc. I am so terrified….I can hardly function. My reaction to antibiotics is not good…I get so sick. The thought of being on them for such a long time freaks me out. It’s like I’m boxed in a corner.
My entire rib cage hurts and he feels the infection and inflammation is exacerbating my costochondritis. When I wake up in the morning and open my eyes, I am immobilized with fear at the prospect of taking that medicine for such a long time….., and/or what will happen to me if I don’t. I pray……
As soon as he speaks to my Opthomologist he wants me to start first with the azithromycin three times a week, then add the ethambutol. He wants my eyes checked every three months.

He said if it makes you too sick you will stop. So then I could develop cavities and not be able to breathe. I’m so discouraged and very scared Sue..

Sue, how did the meds affect YOU.
Any suggestions? Bon

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Bon,
I am going to recommend something I TRULY wish I had done - ask to be referred to a counselor with whom you can share your fears. I was a mess for the first 6-9 months of my treatment - didn't feel like I was getting the best care, scared, very sick (from MAC and Pseudomonas at the same time.) I tried to be strong for my family, my daughter was in a difficult pregnancy... I just became a couch potato unless my 2yo grandson was with me.

By nature and upbringing, I was taught to be strong for everyone else, whether I was or not. I should have stopped saying "I'm okay" to my PCP and asked for help. Talking things out, getting some coping skills, maybe even temporary meds, would have been the best thing.

As for the rest of your questions, the antibiotics aren't pleasant, but not all of them cause reactions in every person. Your doc has your back!

I recommend two things for you to do now:
1) Ask Dr Swenson to have his nurse or assistant available to coach you through the first few weeks. I needed help from my doc's nurse to figure out when to take (bedtime worked for me but everyone is different), how to take (together and with a little starchy food worked best for me) and that certain foods didn't taste good to me while I was on the meds.
2) Ask your primary to refer you to someone you can talk to about your fears.

Can you try these?
Sue

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@sueinmn

Bon,
I am going to recommend something I TRULY wish I had done - ask to be referred to a counselor with whom you can share your fears. I was a mess for the first 6-9 months of my treatment - didn't feel like I was getting the best care, scared, very sick (from MAC and Pseudomonas at the same time.) I tried to be strong for my family, my daughter was in a difficult pregnancy... I just became a couch potato unless my 2yo grandson was with me.

By nature and upbringing, I was taught to be strong for everyone else, whether I was or not. I should have stopped saying "I'm okay" to my PCP and asked for help. Talking things out, getting some coping skills, maybe even temporary meds, would have been the best thing.

As for the rest of your questions, the antibiotics aren't pleasant, but not all of them cause reactions in every person. Your doc has your back!

I recommend two things for you to do now:
1) Ask Dr Swenson to have his nurse or assistant available to coach you through the first few weeks. I needed help from my doc's nurse to figure out when to take (bedtime worked for me but everyone is different), how to take (together and with a little starchy food worked best for me) and that certain foods didn't taste good to me while I was on the meds.
2) Ask your primary to refer you to someone you can talk to about your fears.

Can you try these?
Sue

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Thank u sue for your honesty. And suggestions ❤️

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@rstel7272

While treating the other diseases with the big 3, etc, the cavity may close by itself. I am not so lucky, I have scar tissue in and around the lung. Surgery is an option to remove the bleb, lobe or entire lung.

Jump to this post

I wish you healing and the very best🙏🙏🙏🙏

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@sue22

Hi Tina
Very sorry that you are having more coughing. Are you monitored by a local doctor or NJH during this period? How often do you have sputum cultures . I hope to finish treatment soon for MAC and wondered what the protocol for follow up may be. Thank you if you want to share.
Susan

Jump to this post

Hi Tina,
I cought a lot also. And, I know this is a bandaid but I find a cup of lemon/ginger tea with a big dollop of manuka honey really helps. Or, at night, before bed, I may have a 1/2 teaspoon straight and chase it with a few sips of water.

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