NJH Patients
Hello!
I have an upcoming appointment at NJH for outpatient treatment. I made the appointment upon first hearing about my MAC diagnosis, however...I am not feeling sick in the least! My diagnosis consisted of both CT and sputum positive results. Currently I feel like I should I delay my visit to NJH until when / if I ever feel unwell due to this condition. My kids say go now to nip it in the bud...What to do?
Cheryl
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Thanks for the information. Did you rent a car or you walked? I don’t do well in high altitude - headache- but i will have to survive it I guess. It’s 12 days so where did you have your meals? I am nervous because I am afraid of change of my routine.
Hi Rick, I already started collecting CT cds and notes. Thanks for the advice to check with my insurance how they cover NJH. It’s so much to think about I only hope this visit will happen and will be worth the effort.
No walking to NJH. We rented a car from Enterprise - a shuttle will pick you up at the airport. The hotel has a breakfast buffet that is really good - scrambled eggs, sausage, waffles, Etc. There are several restaurants around for dinner. Valet parking once you are at NJH. Wheelchairs right inside the doors. I was hesitant also and the travel has taken a toll on me. Combine the altitude with 15 degrees and snowing - not good for this FL girl. If you need oxygen they will provide it - I did one day.
The Hampton Inn is no small place - six stories high and fully booked through next week.
I will say going from a pulmonologist that knows nothing - zero - about MAC back home to NJH they are definitely on top of it here!
I forgot to add that the buffet is free.
I like the pulmonologists at Mayo. There are several that are very good.
which Mayo? I have been told that some are far better than others....
The one in Jacksonville, Fl. Is where I go because I live here. The one in Rochester is the best.
I am scheduled to go to NJH in January. I received the packet and the schedule. I start with chest xray and high resolution chest CT scan and see the doctor on the third day. I believe this is a routine schedule they send. I had my CT scan in September and really do not want to be radiated again- how do you communicate this to your assigned doctor and can you avoid certain tests? Did anybody have the same situation and how did you deal with it? I would be grateful for ideas.