At NJH and need to vent
I had very high hopes coming here. The Ambassador screwed up all the dates and ended up planning our first day as the day we fly to Denver. It was a stressful Nightmare. I had to change all the reservations and it cost me a lot of extra money. I figured just be glad you are going and try not to dwell on that. Unfortunately the nightmare has continued. Yes they test a lot. When I saw My doctor ( infectious disease) he was very curt, and hard to talk to. My husband agreed. I told myself if he’s a good dr just focus on that. So he met with me today to go over the ct scan . My pulmonary in Georgia told me I don’t have brochiecstasis , you know, the same guy who said don’t nebulize. I just found out I do have that as well as Mac . The dr was rushed and somewhat irritated with all my questions. It felt uncomfortable . He did want to address the other items not his expertise.
The respiratory therapist is s space cadet who offered NO suggestions. She brought in s different aerobika and left it on the counter overnight. The collect three samples one per day. Second day she handed me the dirty aerobika yo give thenext sample. I figured she would who out a clean one. I said “ I brought one from home I’m not using that dirty one”. Then the BIG LIE CAME AND. I QUOTE”. I told you to wash it. Air dry it and put it in a drawer”. I CAME BACK AT HER AND SAID” no way did you say that to me..”. BELUEVE ME SHE DID NOT SAY IT. She refused to own it and talked to me disrespectfully not to mention that she was ok with me reusing a dirty aerobika with the previous days remnants of saline in it”. She made no effort to talk to me about air clearance tips., which is so important as u all know. I spent a frigging fortune to go here and I’m very disappointed. Boy was I a fool. I’m going to dr swendon ATLANTA great reputation Mac and Brock. Maybe hr’ Ok be more helpful. I could could just cry from deep disappointment. The dr said said it’s up to you to ask the resp therapist questions. Bullshit
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
Truthfully, I'm not sure what these mean. I've never had anyone explain them in detail. I do know that in addition to NTM, bronchiectasis, and a cavitary nodule, I have had pseudomonas, rare yeast, and something else I can't remember off the top of my head. Like you, in the beginning, I looked for anything that would reassure me that I wasn't THAT sick...I still do - only in a different way. My goal now is that everything remain STABLE. As long as the NTM continues to wax and wane, and as long as the cavitary nodule remains the same size or smaller, I'm resigned to accepting that I will die with this disease - not because of it. I know you'll be prepared with your questions on Monday and hopefully get answers that will ease your mind. There may be someone else on this forum that has more information about your results. I'll be interested to know. In the meantime, hang in there until Monday. I've added you to my prayer list. Busy
How did they treat pseudomonas
That’s great thanks
Oh yes , the culture results come piecemeal and can be alarming. I'm not expert but my sputum results often show those Gram positive and Gram negative items. (Positive ones are normal resp flora.) I have had stentotrophamonas and a fungus of some kind aa well as MAC, but have never been treated for anything but the MAC. .. so have stopped worrying about the results (except for the MAC culture!) Certainly ask Dr Daley but these are not necessarily cause for concern. ...
Thks for your response! I do appreciate it. I think that after I discuss things with Dr Daley I’ll feel more peaceful. I’m just scared right now.
My fibromyalgia is off the charts and it triggers the costochondritis which makes me feel out of breath. That really freaks me out…..
Do use ever get out of breath?
I just re read your response and thank you so much. It really helps to communicate with someone who goes thru the same thing, who understands.
My oxygen was 87 the first day I got here, today it’s 93…….
You said, "My oxygen was 87 the first day I got here, today it’s 93……." That's great news! That means your body is acclimating to the altitude. Travel at altitude is scary for me because I can never get my O2 above the mid-80's.
Today we had an air quality alert, and I was outdoors tending to guests - I bet my oxygen was below 93 all day - at 900 feet of altitude.
So I have read more about your tests, and don't see anything alarming.
Also, when you feel anxious or in pain, can you try 4-4-4 breathing to calm yourself? Sit or lie quietly, put your hand on your belly and breathe in through your nose for a count of 4, hold for a count of 4 (if you can) then breathe out through pursed lips for a count of 4. You should feel your belly expand and contract as you do this. As you do this visualize your worry, fear or pain blowing away on your outgoing breath. Repeat at least 5 times, or as long as you need to until you feel calm.
This is a technique I use to calm pain spasms, shortness of breath, angry thoughts... Can you try it tonight to fall asleep without worrying?
Sue
Yes I will try it. So you do get out of breath sometimes? Does it freak you out. No rush to answer..enjoy your celebration! And thanks sue…..
I have had problems with shortness of breath for many years, sometimes really bad, other times almost unnoticeable.
No, I can't say it ever freaks me out, but I was a runner and used to getting out of breath when pushing hard. So I guess I always knew that I would eventually catch my breath. It mainly makes me angry when it is bad and I can't do what I want, like chase grandkids or climb a lot of steps.
Sue
You are so wonderful to share your experience with me Sue. I find its so helpful to share with people who go through the same thing I go through. Sometimes I feel so alone with this. Perhaps after I talk with Dr Daley this week I will have a broader understanding of the “whys” etc and I won’t freak out as much. Thks Sue