How is everybody doing?
Hello All! The forum has gone quite. Haven't heard from some of you in awhile. I am hoping some of you will check in. As for me, I just got ALL of my sputem lab reports going back to 2013 as I had requested. My very last test from June came back negative for everything. Yay!!!! I still battle fatigue and shortness of breath though. There were some organisms picked up in the past that I had not recognized, so I am going to Google them. Look forward to hearing from everyone! -Terri M.
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Hi Sally. Wow, it seems like your U of M physicians are on the ball! Unfortunately, many of us on this forum have also experienced doctors that weren't looking for anything beyond an 'asthma' diagnoses during the on-set of these infections or even having bronchiecstasis. I am relieved for you that you now know what you are really dealing with and can take the steps to take care of yourself. We'd like to hear how your next appointment went for you.
The base-line test post that I sent you is actually a re-post from our former mentor, Katherine, she has left us a treasure trove of great information. If you read from past posts here on this forum; you will find lots of helpful information. (especially on Katherine's post @katemn ) We are glad that you joined our forum. It is a wonderful group of people who support one another. Please feel free to jump in and ask questions or share some news. Just know that myself and others are here for you. Big Hug Sally! - Terri M.
@auntnanny Hi Jan! I came down with MAC in March of 2005. I KNEW I had something terrible and different. I was told it was bronchitis and was giving a weeks worth of antibiotic. I did not get well. I was put on other antibiotics for several months following that. Still, did not get well. Not a one did a sputem test to see what was making me so sick. Finally, I was referred to a specialist at a medical college; and they found the MAC. That was in the end of August. So, I went five months before a real diagnosis. I also learned after getting my hands on all past medical records that I was diagnosed with bronchiectstasis in 1999! No doctor ever told me that! The doctors that got those medical records afterwards never brought it up! I am so angry about that because I would have taken better pre-cautiuons had I known about it. I found out about my bronchiecstasis in 2013 after a visit to the Mayo Clinic from a CT scan.
Thank you, Windwalker -- for more details on how your diagnosis came about. I think I'm just "running scared"...... and lots of things go through my mind. Thank you
@auntnanny Jan, I copy and paste the person's @name and apply it to the replying post. That way the reply will get to that person.
@auntnanny, I will call you. My number starts with 520, so look for me! P.S. any others that feel inclined to give out your phone numbers to someone on the forum, please do it on the private e-mail. It is not safe to put it out on the public forum. Jan, I will have Colleen remove that for you. Will call you now.
Hi everyone! I just completed my second round of antibiotics for bacteria in my lungs, and they didn't work. I first was on Bactrin, then Cipro. I had 2 days of feeling well, then my low grade, 99 degree temp came back with its aches and chills. It arrives at 5 pm and lasts about 2 hours. I will report this to my Infectious Diseases doctor and he will probably want to put me on another antibiotic. Does anyone know of a drug that doesn't cause diarrhea? I'm sure he will want to treat this. robynmar
@robynmar, Hi Robyn! I don't think anyone can answer that question because everybody's body is different. For example, Cipro doesn't bother me in the least. They should have done a suseptibility test when they cultured your sputem. That test should contain a list of antibiotics that will work on your particular strain of bacteria. From that list, you can ask him which ones are less likely to give you diarrhea. Hang in there girlfriend!!!
Robynmar, I just read your post and wanted to say I've had close to similar situations with what you describe -- Bactrim and Cipro. What works for me a clindamycin and a probiotic (30 million size) -- any brand ---- and I get along with that and it works for me. Again, it really depends on which type bacteria they are trying to treat. Levaquin is another possibility -- but I would go for the clindamycin -- 150 mg 4 times daily ----- or you can do 300 mg twice -- I've done both. Hope this helps
Auntnanny....do any of your Doctors do chest CAT scan? Tdrell
tdrell ------ I had a cat scan at Mayo's two years ago when I was diagnosed. And..... had another one about 3 weeks ago locally. Sent a copy of the scan to Mayo's and my pulmonologist there wrote me a note saying some of the scan looked a little better than 2 years ago and the rest was about the same. I was hoping nothing had worsened so I felt good about that.