MAC Big Three Side Effects
A few months ago I was diagnosed with Primary Immunodeficiency. My body has stopped producing immunoglobulin G. Next week I'll begin infusion therapy to replace it in my body and repair my immune system. About two months later, I learned I have MAC and bronchiectasis. About a month after I start my infusions I'll begin my antibiotics for MAC.
I'm interested in knowing about others' side effects from the big three. I'm also interested in how you manage your side effects. I know this information will really put my mind at ease. Thank you in advance.
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
My thought as well. When he said I was going to die it wasn’t said with even an ounce of compassion but rather anger as if a personal loss for him. I was in total shock in the difference in him from my first visit when he told my husband and I he was going to take care of me. I called Mayo a few months ago trying to make an appt but was told they didn’t accept our insurance. I will look into NJH and NTM.
I also have thought that there may be a connection between how long I’ve been on the 3 meds and the side effects I am now experiencing. The severe dizziness just began about one year ago but I’ve been on the meds between 2-3 years. I hadn’t asked or even considered side effects that could be attributed to the meds. I was surprised when I did a search on all three and found side effects attributed to all three. Vision and hearing can be affected. I’ve noticed a little difference in my vision and my eye doctor today told me I now have 20/30 vision with corrective lens instead of 20/20 but he said that is still good. However I have noticed a huge change in my hearing.
Have you had your hearing tested while on the meds? The standard is every 6 months, with consideration of stopping the meds if it declines much.
Also, has the doctor recultured your sputum and done new sensitivity testing? Maybe the remaining bacteria is resistant to what you are using. Or, if the colonies have declined enough, maybe switch from drugs to rigorous airway clearance with 7% saline.
I did that at roughly 19 months, because the side effects were intolerable for me. My slings continued to improve for the first year, and are now stable. I'm sure the MAC is still hiding in there, but I keep chasing it with the 7% saline.
Roughly where in the US are you located? There are excellent HTM docs in quite a few places now.
Sue
I have learned more about MAC in a short time than I have from doctors since I was diagnosed. We have had the same Optometrist for 15 years and have a close relationship with him. I told him yesterday that I had noticed a ‘slight’ difference in my vision but a major difference in my hearing. I know now from this site that I should have had my hearing tested before now but can only move forward and get it tested ASAP.
I understand that MAC is rare but it sounds as if too many of us learn as we go. I had to go online to find out how to use my nebulizer. On my last visit I asked my pulmonologist’s assistant if they had treated anyone with MAC. This is my regular doctor who I’ve gone to since my diagnosis. Even though she told me they had I still question whether they have with all the lack of info. I feel like he is passing the buck for a better way to describe it. I have had sputum cultures and all show the bacterial infection. A chest x-ray in Dec 2022 showed twice as bad compared to Dec 2021. No one mentioned side effects to the three meds.
How would they do sensitivity testing? I don’t believe there has been any previously done. The first I’ve heard of including an infectious disease doctor was on this site. It is a case of learn as you go.
I live in Seminole Florida just below Tampa. What is HTM?
Thank you again Sue. I’ve learned more from this site and you than I’ve learned in 3 years from my doctors. It’s almost like they don’t want to tell you that this is not curable and the best we can hope for is remission. I understand that to a degree but I believe sharing important info like get a baseline hearing and vision test as soon as we are diagnosed would be important. My husband just said he has no faith in my pulmonologist. He is a very nice and compassionate doctor who I suspect has not treated anyone with MAC. I placed a lot of hope in the doctor he referred me to after the first appt but I’m not exaggerating when I describe him as Dr. Jeckle / Mr. Hyde because I walked out of my second appt with no hope. I’m doing everything I can to gain weight but being told I was going to die if I continued to lose weight after losing another 1 lb 4 oz in 6 weeks hit me like a ton of bricks. I was depressed for a few weeks but I finally decided to take everything I’m learning here and go forward. First - get my hearing tested. Second - find an infectious disease doctor. Third - who do I contact for sensitivity testing?
I didn’t address one thing the Guru said during my first appt - that maybe I had built up an immunity to one or more of the big three. “We might have to add a 4th med. No mention of that during second appt.
If you are in Florida, have you considered contacting Mayo in Jacksonville for a consult?
http://mayocl.in/1mtmR63
Sue
Yes I called several months ago but was told they won’t accept our insurance - Aetna Medicare.
I have medicaid advatage freedom plan
Ppo. Mayo doesn’t accept but national jeeidhesth in Denver does so gonna go there soon unhook whicdebddm. X
I have been on Hizentra for several months for my immune deficiency. I with my daughter's help infuse it subcutaneously every week and so far I have had no side effects.
Hi dlynn
Definitely reach out to National Jewish Health!!
In the interim, I am part of a support group near Tampa that meets every month. This is a wonderful group of women with NTM and live in close proximity to you with good pulmonologists and ID docs. Next meeting is a week from today on April 26. Please message me your email and I will send you the link.
Sending you positive VIBES!
Dee