Jewish hospital appt
Hi yesterday i got my call from denver to schedule my appointment for a second opinion. It will happen in march. Its a two week schedule, they say i will have lots if test
I know some of you have been there could you share your experience and did you get answers. I have been on 3 meds for almost a year and started arikacy 1 mo ago. I was diagnosed as mild to moderate but still positive. Its crazy.
Per my infectious diseases due to bronchiectasis the probability of mac returning is pretty high.
Thanks miriam
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
I also thought you might get tested for CF. The test is expensive and might not be covered but sounds like you should consider it. I had the test and mine came out negative. Has your pulmonologist considered putting you on Pulmozyme? It is helpful for those with CF that have very thick and difficult mucus. Some say it is not recommended for Non CF Bronchiectasis however. I asked my Pulmo about that and he said it was based on only one study and that they have found it helps some people with Non CF Bronchiectasis. It is very expensive and also may not get covered. I spend about one and a half hours on airway clearance a day and i think that is more than average. So 4 to 5 is a lot.
I would try to get an appointment with Dr Daniels if you can as she has a lot of experience with Bronchiectasis and Mac. Where in NC do you live? I am in Wake Forest/North Raleigh area.
I am trying to see if I can clear MAC by doing Airway Clearance and Dr Daniels is in agreement. I don't have any symptoms of MAC but I do have high colony counts and sometimes I am Smear positive. Do you have any side effects from taking the drugs? I am praying for you that you can remain clear and just be done in 6 months. Do you live in NC? Happy New Year!
Sue, I also have chronic post nasal drip. ENT and the Allergist have Rx. 3different nasal sprays. Each helped with the sinus drainage but all cause chest tightness and difficult breathing Azelastine HCl; Mometasone Furate;
Irpatroplum Bromide; and I have tried over the counter nasal sprays (Fluticasone Propionate). I have also tried
Xlear Nasal spray but that makes my nose bleed after about 3 days.
Nettie pot using filtered and boiled water and saline packets 2 or 3 times a day helps wash out the mucus from my sinus. It is sometime depressing because no matter how much time I spend cleaning the head and he lungs, the amount of mucus does not diminish,
I also have hiatal hernia with GERD
Head of Bed on blocks about 6" and no food or beverage for 3 hours before going to bed and avoid acid foods and beverages.
I live in Wilmington now, but lived and worked in Raleigh for MANY years, I will see if I can get an appointment with her without hurting my Docs. feelings
I also searched after someone mentioned Dr. Kenneth Olivier. He has impressive experience and he is at UNC-CH Pulmo Clinic. now.
Thank you. That is encouraging.
Yes, I did a little searching on line this week and she is a "fellow." I have been going for a little over a year. I will find out if Dr. Daniels is still working with her.
Someone wrote a few months ago about wanting to cry each time they start the daily airway clearance. I can relate to that. This group has made me realize that the amount of time I am spending is excessive. The Respiratory Therapist told me to use nebulizer for 10 minutes and STOP!! I would have died from not being able to breath months ago, if i had followed her instructions! She also works in the Peds. clinic part of the time.
No! I have not been tested for CF gene, but I will contact the pulmo in UNC_CH and ask about that since she sees children with CF in the Peds. clinic.
I had been advised to do 'watchful waiting' by 3 different community doctors, including 2 at Mayo. Their rationale was that 'the treatment was worst than the disease'. Therefore, I had not taken any meds prior to my NJH visit. During my 2nd meeting with my NJH doctor, I was told that I should start meds ASAP, even though I was still asymptomatic.
I believe about 17% can clear MAC via airway clearance. I was not able to clear my MAC, but I was able to dramatically decrease my colony count from over 200 to below 20, so it can still make a dramatic difference.
I am now 2 1/2 months into the Big 3 and have been doing well on them. I go to NJH May 2nd and am anxiously awaiting my visit.