Re: How many doctors did you try until you found a good one?
Posted: Sun Sep 01, 2013 5:39 am
My first Sleep doctor 13 years ago was a total ass. When I had no improvement from EDS after six weeks on CPAP, he said, "Then you don't have sleep apnea." This was after a sleep study showing moderate sleep apnea with AHI of 28. I went it alone for 12 years on the pressure he prescribed all on my own and eventually saw improvement after switching my blood pressure medication (ACE inhibitor).
When EDS returned last year with a vengence, I sought out a new sleep doctor associated with a new sleep clinic. When I had my first study 13 years ago, there were only two sleep clinics in my area and both were hospital based. I had to sleep in a room with glass windows for techs to observe (fish in fishbowl and too much light in room) and a portapotty at the bedside (techs could watch through glass) since the wiring could not be disconnected. Now there are 15 sleep clinics in my area and they are high tech with hotel-room like ambiance. They have video cameras instead of glass windows and quick disconnect to use the bathroom.
I chose a female sleep doctor who was also a board certified psychiatrist. I felt she could better understand the effects of my psych medications on EDS. Turned out my AHI had gone from 28 up to 71 over those years. At first she was adamant that she did not want her patients to have data-capable CPAP. Her explanation was that "patients don't understand any it anyway." I got a ResMed Elite anyway and when I returned after 30 days, brought graphs and had a great talk with her about what my data indicated. She upped my pressure at my suggestion. She totally changed her mind about patients having data-capable machines saying some can benefit from monitoring their own sleep data. I have a great relationship with her. She sees me every 6 months.
In January, I told her I thought I needed BiLevel because I was having difficulty exhaling against CPAP at 18. So she wrote an RX for BiLevel writing "failure at CPAP" on RX so Medicare would cover it. Also wrote "Mask of Patient's choice."
I have an appointment to see her in 1.5 weeks and look forward to reviewing my data with her.
I would hope that most people with OSA see a board-certified Sleep Doctor. Those that depend on general practitioner, ENT, or other specialists will NOT get the same expertise as a Sleep Doctor. They have far less experience with monitoring patients on PAP therapy and will be of little help in resolving adjustment problems.
After my experience with the first JACKASS, I've found a great Sleep Doctor to see as long as live in this area.
When EDS returned last year with a vengence, I sought out a new sleep doctor associated with a new sleep clinic. When I had my first study 13 years ago, there were only two sleep clinics in my area and both were hospital based. I had to sleep in a room with glass windows for techs to observe (fish in fishbowl and too much light in room) and a portapotty at the bedside (techs could watch through glass) since the wiring could not be disconnected. Now there are 15 sleep clinics in my area and they are high tech with hotel-room like ambiance. They have video cameras instead of glass windows and quick disconnect to use the bathroom.
I chose a female sleep doctor who was also a board certified psychiatrist. I felt she could better understand the effects of my psych medications on EDS. Turned out my AHI had gone from 28 up to 71 over those years. At first she was adamant that she did not want her patients to have data-capable CPAP. Her explanation was that "patients don't understand any it anyway." I got a ResMed Elite anyway and when I returned after 30 days, brought graphs and had a great talk with her about what my data indicated. She upped my pressure at my suggestion. She totally changed her mind about patients having data-capable machines saying some can benefit from monitoring their own sleep data. I have a great relationship with her. She sees me every 6 months.
In January, I told her I thought I needed BiLevel because I was having difficulty exhaling against CPAP at 18. So she wrote an RX for BiLevel writing "failure at CPAP" on RX so Medicare would cover it. Also wrote "Mask of Patient's choice."
I have an appointment to see her in 1.5 weeks and look forward to reviewing my data with her.
I would hope that most people with OSA see a board-certified Sleep Doctor. Those that depend on general practitioner, ENT, or other specialists will NOT get the same expertise as a Sleep Doctor. They have far less experience with monitoring patients on PAP therapy and will be of little help in resolving adjustment problems.
After my experience with the first JACKASS, I've found a great Sleep Doctor to see as long as live in this area.