Options if MAC goes untreated
MY ID Doctor took me off the "BIG 3" last October because I wasn't able to produce any sputum (never have). Had a CT-Scan done in January showing the MAC is still and Bronchiectasis has gotten worst. My Pulmonary Doctor got in touch with ID Doctor about putting me back on the "Big 3". The ID Doctor won't, she called in a prescription of propranlol. Many years ago another doctor prescribed that for me. I had the worst reaction to that. There is no way I am going to try that drug again. So what happens if I don't treat the MAC?
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
Just curious if anyone who has been using 7% saline have their lips, tongue swell and get thin skin inside their mouth and lips? Not fun!!!
Not something I have experienced, but a number of the other meds like levalbuterol can also cause this. When I am using nebulized meds., or if I get mouth sores from something else, I use a mouthwash for sensitive and sore mouths - which one I buy depends on what the local Walgreens has at the moment.
And sometimes, I lean on old-fashioned Lavoris, which contains cinnamon, anothrer soother.
Is arykace expensive
Yes. But there are programs that you my qualify for assistance with cost
Thank you
Sue I saw a comment you made I don’t know when. But you said that Mac and Bronchiectasis is something you have to leave with like other diseases. Such a positive attitude and made me feel a little better. I go to njh in November they say they can help but if not I am going to try and have your attitude. Thank you
Oh yes, NJH can help - help you to live your best life, with or without Bronchiectasis and MAC and with or without antibiotics. They will teach you the best way (for you) to do airway clearance, cover lifestyle issues like exercise, diet and rest, maybe offer tips to help ease anxiety.
Trust me, in early days, I was where you are - I thought I had to change the way I did everything, I would never feel well again, etc. Time, experience, wise doctors and the wonderful members here have taught me to just make it part of life.
And of course, we are always here to encourage you.
Sue
Thank you. I so appreciate your time. Trying to not be anxious but very hard. Not used to having these health issues
Also. So glad I found this web site. So helpful and informative and reassuring
I bet if you asked 100 people here if they were anxious, scared, and confused at their diagnosis, at least 95 would say "YES"
We're here to hold your hand, just ask