MAC antibiotics and side effects
Hello. My name is Renee and I live in Australia with my husband who was diagnosed with MAC in Sept 2014. At the same time he was also diagnosed with Hodgkins Lymphoma, COPD and hereditary emphysema. He also has adrenal failure we’re told from the chemo. He is currently in hospital on a iv antibiotic drip of tigecyline and oral antibiotics. My question for those of you that have taken rifubutin and moxifloxcin. How long did your side effects last? Did they ever diminish or completely go away? One of the reasons he is in hospital is due to the severeness of his side effects. Constant headache, muscle aches, body temp regulation and shortness of breath. He has been on the tablets now for a 4 weeks. Thank you!!
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@macjane….a student nurse that I had years ago suggested that movie with William Hurt was best she had ever seen….since I was retiring….I had time to watch it….agree….it was awesome….wish I could have had every student nurse watch it!
I loved at end when Hurt had medical students give each other enemas to see what it was like. Tdrell
You are absolutely right. It wasn't John Hurt but William Hurt……….I loved the ending…………..it was perfect. John Hurt is an actor but not in this movie. Thanks for the help…………..Jane
Thank you for this. I have given up trying to describe to family and friends how I feel. I answer OK to every inquirer. How can you explain that at eleven o'clock you feel on the edge of fainting, too fatigued to carry on but two hours later you may be your old self. .
@flib, That is good know, thank you for posting.
@mary1944, Hi Mary. My Mayo doctor is treating me by using alternating antibiotics. He uses doxycycline for 10 days one month, then Ciprofloxacin for 10 days on alternating months. This may not be an option for you because I do not know what kind of mac you have, but you can ask your doctor if that is an option for you. I was put on that regimen in 2013. I did contract pseudomonas in 2016 and the doxycycline was replaced with tobramycin for 28 days. that got rid of the pseudomonas infection.
Terri, I am hoping to hear from my pulmonary doctor today as I need to know more about what he is thinking might be some good steps forward with my care. This site is so informative. Many thanks.
@flib I know what you mean; it is hard for people to understand the debilitating aspect of the fatigue that comes and goes. Especially when we look fine on the outside. Have your family members look up this disease and read about it. Or let them see posts on this blog. I have had this disease & fatigue for years; but, because I maintain a cheery attitude my husband constantly forgets that I have it. He asks me to do things like take a long bike ride, etc. I did try to yesterday, but couldn't make it out of the neighborhood.
@flib We have what is called 'Pluff Mud' here in coastal S.C.It is found down by the water's edge. It is mud that you can sink up to your knees in. It is very thick and will suck the shoes right off of you. Plus it it very difficult to get out of it and people have been known to need rescue from it. When I am having a very bad fatigue day I tell my husband that I am a stick in Pluff Mud. That way he knows the level of fatigue is very bad and not to expect much from me.
@macjane, I am going to watch this movie this week. Thank you for sharing.
@flib Terri @windwalker is right about encouraging your family to read about these topics. You can send them the links to articles that you want them to read so they don't feel puzzled about where to look or what words to use to search for them. Before my diagnosis with bronchiectasis and MAC, my husband used to complain about me not taking care of myself enough to ask for stronger cough suppressant from my doctor every time I coughed or tried to clear out phlegm that made a lot of noise. At that time, neither of us knew what I had. But I just knew that cough suppressant was not going to help. We would argue back and forth endlessly to no avail. Fortunately, my husband is a avid reader of any and all subjects that are of interest to him. After the diagnosis, he spent a lot of time reading about bronchiectasis and MAC and realized that using cough suppressant would have been the wrong thing to do in my situation. Nowadays, he would instead ask me whether I have tried to clear the phlegm out when he does not hear the noises for a while. I no longer need to explain myself and there is no more complaint, only concerns.