MAC advise
Hello everyone
Its been while since I wrote to you all. I wanted to get some thoughts on your experiences after taking the meds and how you did.
I have been taking the 3 meds for MAC now for 9 months and my sputum is still positive. I have no major side effects but I feel exhausted all the time and not well.
My ethambutol was increased last month. I just feel like the meds are not working. I thought since they said I was mild to medium infection that it would clear it up. I guess I wasn’t as mild as they thought. My lung ct are not cleared either.
I do albuteral, saline 7% on my nebulizer and a flutter valve . I really do not see much help getting my sputum up.
My infectious disease doctor wants to send me back to Duke for another opinion. Don’t know about that. I was thinking maybe getting her to get me an appointment at Jewish health hospital for an opinion.
Would like to hear your thoughts. I am at a crossroads and need help.
Thank you all
Miriam
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
Hi, I had a VATS...video Assisted Thoracic Surgery. The surgery didn't take long, like 45 minutes. A person is usually in the hospital for 4 days and you have a drainage tube for 2-3 days PO. One may have nerve pain, I think that was the worst for me and the fact I can't take narcotics as I throw them all up. I don't do well with Tylenol, etc. either. They really don't want people to throw up and have that go into your lungs. I also had a particle lung collapse while in the hospital. One day I had 6 x-rays! So it was probably more painful for me than others...as they had to keep any pain meds at a minimum including Tylenol. After I got home, I sporadically took Tylenol or Ibuprofen for pain as needed for about a week. I had to get off those too then as my stomach couldn't take it any longer. Took about 4-6 weeks before I was feeling more myself again, I had lost more weight and my labs were all messed up and took that long to get back to eating again, etc. Hope this was helpful!
Question on the inhaler amikacin. Would like to hear about experience with this med. my doctor prescribed it as next step because i have not converted after 10 mo of the 3 meds.
Thanks
Miriam
I've been on inhaled Amikacin since March. I have 5 neg sputum since then. Cautiously optimistic. I lost my voice but it slowly got better. Be sure to have your hearing checked routinely.
Thats good news. Getting my hearing checked and glad to hear not many side effects except hoarseness.
Thanks
Was that the only medication you were taking? Have you been nebulizing or anything else to support the treatment?
Thanks
I nebulize Albuterol and 3% saline 2x/day, Anoro 1x/day, use the aerobika, use a percussion vest 2x / day and I'm also on the Big 3 everyday. I have cavitary MAC.
Try to get appointment at NJH in Denver they are the best. Best of health!
You sound pretty much just like me. I'm doing the Big 3, Albuterol, 7 % Saline & Arycayce. Not sure if I'm improving much as I now have very deep chest cold symptoms. My doctors are really not being too helpful and I see a bunch of them. Need a new plan of sorts and I'm "up for ideas" as well!
I took have little hope for a future....My MAC has grown and I am doing every thing possible. I now have a 2nd mass from the CT results not previously seen. No call from my MD to advise. Just waiting for my next appointment. Trying to process this. This is the 1st I have said anything. Can't even discuss with my family as there trying to be optimistic.....Prayers for all.....
It seems old woman's disease is not a very popular disease to investigate and improve the quality of life. I feel that there's very little but ancient remedies. I'm interested in everyone's input as to help! Best to you all! It's a very lonely disease. I fight it by doing a rigorous aerobic activity every day possible, staying positive, and fighting like heck all along the way. Professionals want to help, but the research needs to be there. It's not a disease that has money coming its way. Prayers to you all and keep seeing answers.