MAC: Anyone ever felt pain from MAC? So many questions

Posted by jr2366 (Jennifer) @jr2366, Dec 17, 2020

I was just diagnosed with Mac lung disease Just few weeks ago I would like to know if there’s any body who can give me some positive advice for me as I’m just learning about all this I’m currently on medication it’s an inhaler daily for this which I only started 2 days ago I have a year to 18 months to stay on this dr says. Medication is called Arikayce has anyone else been in this medicine ? I was wondering has anyone ever felt pain from MAC also. So many questions I’m sorry but any advice would help a lot thanks Jennifer

Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.

Any suggestions for how to lay flat and still without coughing up phlegm for an hour (MRI/MRV with and without contrast)? This test is unrelated to my Chronic Asthmatic Bronchitis. But I am scared of choking while I wait another few months for my appoint at NJH — thanks for any suggestions.

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@jamieh

Any suggestions for how to lay flat and still without coughing up phlegm for an hour (MRI/MRV with and without contrast)? This test is unrelated to my Chronic Asthmatic Bronchitis. But I am scared of choking while I wait another few months for my appoint at NJH — thanks for any suggestions.

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I can certainly relate to your problem. There are a few things that work for me. However I have Bronchiectasis and not Asthmatic Bronchitis. Not sure if what I do will work for you. Since most of my productive coughing happens in the late morning I try to schedule the MRI for early morning or afternoon if possible, and I will also do my daily postural drainage and manual chest percussion a good hour before the MRI if at all possible to get up most of the sputum. And I know you are not supposed to suppress a productive cough, but I will take a regular dose of codeine cough syrup about 30 minutes before the MRI, on an empty stomach so as to get quick absorption. You will have to talk your Dr into an Rx for that. Sue @sueinmn may be able to advise you better with this. Good luck, Bill

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Incredibly nice of you to share your prep routine. Makes me feel less weird asking. I don’t yet have the procedures you mentioned. I really need a better pulmonologist and MAC testing lab. Btw— my husband and I have had 7 standard poodles over the years. …

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@masydnor

Hi, I am new to the group. Has everyone with MAC given up dining out and groups??

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When we eat out, we are very selective. I avoid salads and choose only cooked dishes with cooked vegetables. I used to eat a lot of lettuce, uncooked spinach and herbs. But now, I avoid all of them unless cooked. I also avoid fresh strawberries and mushrooms.

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Hi Jennifer, I just joined. Been battling lung issues since January and finally diagnosed with MAC after bronchoscopy. My pulmonologist started me on the 3 antibiotic today. Started me slow, taking just the azithromycin today, I will add another antibiotic Monday and finally the third Wednesday and will be on them all moving forward. I’ll be honest, I’m scared and all I know to do is pray and let God take the wheel. I appreciate this forum and the kindness and support that I’ve been reading. It has given me hope and less anxiety about this dreadful infection. God bless you Jen and everyone else on here.

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@coder

Hi Jennifer, I just joined. Been battling lung issues since January and finally diagnosed with MAC after bronchoscopy. My pulmonologist started me on the 3 antibiotic today. Started me slow, taking just the azithromycin today, I will add another antibiotic Monday and finally the third Wednesday and will be on them all moving forward. I’ll be honest, I’m scared and all I know to do is pray and let God take the wheel. I appreciate this forum and the kindness and support that I’ve been reading. It has given me hope and less anxiety about this dreadful infection. God bless you Jen and everyone else on here.

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Hello and welcome to Mayo Connect. Jennifer has not been active here for a while, but we have many other helpful members.

The diagnosis of MAC and Bronchiectasis can be unsettling, as few of us have ever heard of these before.
Here are some great places to begin reading, just click on the links
https://connect.mayoclinic.org/discussion/resources-for-the-abcs-on-bronchiectasis-and-mac-ntm/
https://connect.mayoclinic.org/discussion/macntm-is-different-for-everyone-treatment-might-be-different-too/
At first it seems we have more questions than answers. Along with the other members, I am ready to try to answer whatever your concerns are.
I hope this diagnosis and medication start you on your healing journey.
Did you doctor talk to you about airway clearance as one of the ways to get healthy again?
Sue

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@irene5

@jr2366 Yes Jennifer- welcome! Gina is correct. Many of us are now on Arikayce. And welcome! I will start by saying you will glean lots of information and insight into this disease from the people on Mayo Connect. I actually have a question for you. Did your doctor say why he went straight to Arikayce? It is my understanding that Arikayce is used for retractable MAC which is MAC that hasn’t responded to other treatment, is worsening, and/or the patient can’t continue on all of the previous meds. Arikayce is also $133,000 a year - around $ 11,000 per month! I had to apply for assistance with that huge piece. And there is paperwork back and forth in order to be approved for the phase 3 clinical trial that Arikayce is now in. Many people on this site have MAC but symptoms don’t warrant treatment. What symptoms do you have? Do you have a pulmonologist and an ID doctor? Did you get a second opinion? How were you diagnosed? Did you get training from a nurse on the use of Arikayce? It is quite a process and the nebulizer etc all have to be washed in special soap and sterilized afterwords. I’m just realizing I have lots of questions for you. I guess Jennifer I am just surprised that you are on Arikayce and no other MAC meds. If you google Arikayce it will tell you all that info. The only difference is that now you only need to be successful with two of the three other meds. Wishing you all the best, but please do your due diligence about this disease, and make sure you have doctors who are on top of your situation. Ask how many patients with MAC they have treated. Good luck! irene5

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Hi Irene, do you have a contact info for the Arikayce study please? Also, any contact info where you apply for the grant to get it? I may need it. Thanks, Magdalena.

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@mimifeels

Hi Irene, do you have a contact info for the Arikayce study please? Also, any contact info where you apply for the grant to get it? I may need it. Thanks, Magdalena.

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Magdalena yes I do. I’m dealing with a my GSD Simba this morning as he has an ear infection , but I will get back to you later today with that information. Irene

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@mimifeels

Hi Irene, do you have a contact info for the Arikayce study please? Also, any contact info where you apply for the grant to get it? I may need it. Thanks, Magdalena.

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The Assistance Fund 8427 Southpark Circle Suite 100 Orlando, Florida, 32819. The website is http://www.tafcares.org. I hope you will be as fortunate as I was in receiving help from them. I never could have afforded Arikayce. We are rich in children not money. Blessings, Irene

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Hello, I’ve experienced much pain with MAC. Like a tight band around rids and severe back pain. Just a heaviness in my left lung in back now. Also, have felt things moving in my back. My ID Dr says pain isn’t a symptom of MAC but my primary care Dr knows patients that report pain

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