Hello Guest, Welcome to Apnea Board !
As a guest, you are limited to certain areas of the board and there are some features you can't use.
To post a message, you must create a free account using a valid email address.

or Create an Account


New Posts   Today's Posts

CSA and Diet? your thoughts/experience please.
#1
CSA and Diet? your thoughts/experience please.
CSA and Diet? your thoughts/experience please.

CSA and Diet? your thoughts/experience please.
 
Some background before getting to the diet question and why.
 
I am a 65-year-old male and I deal with CSA I believe resulted from a traumatic head injury in high school (a serious blow to the base of my scull…knocked unconscious, concussion, no hospitalization).  I have known that I frequently stopped breathing while sleeping since my marriage in 1974 when I was 18 as my wife of 47 years will testify.
 
It never occurred to me I should be concerned until my CSA made a dramatic manifestation of itself in 1993 on the South rim of the Grand Canyon at an elevation of 6600 ft. in the form of Chain Stokes Breathing…For the three nights I was at 6600 ft. I thought I was dying. It subsided when I returned to a lower elevation, so I just chalked it up to the elevation and took no steps for a diagnosis until 2007.  I retired from my career occupation of construction in 2006 and took up wooden yacht construction at sea level in Thomaston ME.  Within a year my breathing degenerated into a nightly marathon of waking gasping for air, falling asleep, waking gasping for air, repeat-repeat-repeat….
 
I left the boatyard in 2007 thinking my degrading condition may be related to the work environment and while I still had insurance coverage from the boatyard, I proceeded to have two sleep studies back-to-back.  I was convinced from research that what I was experiencing was CSA.  From the sleep study reports my pulmonologist insisted it was obstructive while I was still convinced it was CSA. Being compliant I started CPAP treatment.  I was told to give it 6 months in a let’s see what happens approach.  I got no follow up calls, was not asked to do any follow up visits, gave it the 6 months, and never went back.  CPAP had no effect, so I just lived with it.  Since then, my episodes settled into a cycle of what I refer to as mild, moderate, and severe. (Not necessarily in that order)
 
At the time I was inexperienced and had no backup from a forum like Apneaboard…Only recently have I appreciated from members on the Apneaboard that I had to advocate for myself and give no quarter if I expected any help from my providers. I am so grateful for the advice and answers I solicited here at Apreaboard.
 
On the advice from members, I began to advocate for myself and got the attention I thought was appropriate.  However, I have never stopped researching for possible treatments that could/might/maybe have some positive outcome.
 
As I’ve gotten older the apnea settled into a mild to moderate cycle and my ability to function and work degenerated to the point that last fall (2020) I was only able to work 3 – 4 hours a day 2 – 3 days a week…the rest of the time was for resting as sleep was so elusive.
 
At this point it was time to see my GP who ordered a home sleep study (no three month wait).  With that an appointment was made with a pulmonologist (same one from 2007) this time my pulmonologist spent over two hours with me and concluded…positively…what I was experiencing was CSA and prescribe a Airsense 10 autoset to start with.
 
After 3 months of treatment and adjustments to settings and equipment it was determined by my pulmonologist that my Airsense 10 autoset had no positive affect on my condition.  He decided to move me on to a BPAP machine and scheduled a sleep study.
 
However about 3 weeks prior to this conclusion...I made a major lifestyle change that dramatically improved my ability to sleep through the night...undisturbed.  It should be noted that the first half of the night on my equipment proved pointless (4 hours for insurance compliance) having no effect on my apnea.  The second half of the night was always better, off the equipment.
 
So…I would like to share recent developments and what led to them…I recently happened upon a documentary (Fat-A Documentary).  In part of it they spent some time on how a high fat, low carbohydrate diet could dramatically improve/lessen the frequency or totally stop seizures in childhood epilepsy.  One person they interviewed in the documentary is J.J. Abrams the Hollywood director who has a son with epilepsy.  Abrams sons seizures were dramatically reduced within two days after starting and totally stopped a short time later.  Abrams founded the Charlie Foundation (look up the website. Lots of related information.
 
The foregoing information led to researching Ketogenic diet and its association with neurological disorders like epilepsy.   
 
Additional research led to a plethora of articles on the National Center for Biotechnology Information, US National Library of Medicine website. On the website type in (ketogenic diets neurology) to find the articles.
 
My conclusion was that since CSA is a neurological issue.  The brain simply stops telling a person to take a breath…why not try a high fat low carbohydrate diet.
 
Consulting my GP, I changed my diet from a well-balanced doctor recommended program to a high fat, low carbohydrate diet...basically a Keto diet.
 
I continued the use of the of my equipment during the three weeks leading up to my pulmonologists prescribing discontinued use of the CPAP equipment.
 
I didn’t notice any change while using my equipment until I took a break from using it several days in…I slept through the night with little disturbance.  The best night sleep I’ve had in thirty years.  I continued the use of the machine while I had it, to see if it might measure some differences.  The differences it reported were enough that when I visited my pulmonologist two weeks later…the first words out of his mouth when he entered the exam room were “what have you been doing?”  While my events have decrease little, the duration and type of event have.     
 
Before the diet change, one of my complaints to my doctor was that using the equipment was just as disruptive to my ability to sleep/rest as the disorder itself.  While I had the machine and didn’t have to remain in compliance for my insurance coverage, I stopped using the machine for two or three days at a time and slept wonderfully.  I would then use the machine hoping it would record why?  It didn’t…each time I tried to use the machine I had a really disrupted 4 hours use…then I took it off and it was better.  The following night without equipment use was yet again wonderful.  Tried the equipment…had a terrible night.  The machine reported all my apneas as usual.
 
Based on the machine reports, my doctor ordered a sleep study for Thursday August 19, 2021.
 
Up until this most recent study my nightly sleep without the equipment has been wonderful.  When I arrived for the study, I learned that it was to be done using a BIPAP machine.   Having slept so well since the diet change it made more sense to me to do a split study to see if we might set a new benchmark for the second half of the study.
 
While we waited for the response from my doctor the techs wired me up and put me on the BIPAP machine while waiting to hear back (approximately 30 to 40 min on the machine).
 
My doctor said yes…that makes sense, so I was taken off from the BIPAP machine for the first half of the study.
 
I had the worst night in 2 ½ months and ended up not having enough time for the second half of the study.  The following nights since, my sleep has been sweet.
 
Since the diet change, 2 ½ months ago, I have gone from being able to work 2 - 3 days a week 3 – 4 hours a day to 7 days a week 8 – 14 hours a day.  I’m self-employed and in the marine construction industry.
 
A few questions:
 
Has anyone out there had a similar experience with a diet or lifestyle change?  If so, would you share it?
 
Is it possible that being on the equipment exacerbates my condition?


Is it possible that being on the equipment for the first half of the night disrups the breathing rythm for the rest of the night resulting in a less than best second half of the night?
 
Does it make sense to request a home sleep study for several nights just to see if through the night I’m having any events even though I’m sleeping so well? (I know it won’t determine what kind of events)
 
Is it possible that being on the BIPAP machine for 30 – 40 minutes in the most recent study, spoiled the study? 
 
 
Thank you for your patience…I’m just waiting now to here from my doctor for a review of the study and  what the next step is if any.
 
Kind regards,
 
BFair2all
Post Reply Post Reply
#2
RE: CSA and Diet? your thoughts/experience please.
Can the PAP equipment make CA worse? Yes, if it's not the right machine. In your case, you aren't on the right one. Regular BPAP without backup rate can make your CA come out very strong. I had a similar experience when on a BPAP without backup rate, that's a key phrase in Central treatment.

The correct machine? ASV, the only one designed to actually treat Central Apnea.

Centrals are very much consistently inconsistent.

If your diet change has made you feel better, good for you. There might have been something you changed that alleviates Centrals. But note that if/when Centrals return, you'll want the ASV to treat.

I would recommend you note the following machine name in full, ResMed AirCurve 10 ASV. That is the machine that will treat CA.
Mask Primer

Positional Apnea

INFORMATION ON APNEA BOARD FORUMS OR ON APNEABOARD.COM SHOULD NOT BE CONSIDERED MEDICAL ADVICE. ALWAYS SEEK THE ADVICE OF A PHYSICIAN BEFORE SEEKING TREATMENT FOR MEDICAL CONDITIONS, INCLUDING SLEEP APNEA. INFORMATION POSTED ON THE APNEA BOARD WEBSITE AND FORUMS ARE PERSONAL OPINION ONLY AND NOT NECESSARILY A STATEMENT OF FACT.
Post Reply Post Reply
#3
RE: CSA and Diet? your thoughts/experience please.
Hi Dave

I'm assuming that my caregiver started with the airsense 10 auto and moved to bpap as a process of elimination for the insurance company...does that sound correct?  How many machines am I going to go through to get to the Resmed Aircurve 10 ASV?

Ted
Post Reply Post Reply
#4
RE: CSA and Diet? your thoughts/experience please.
If you follow the path I did, demand Titration with ASV now. No other machine but ASV is the right answer, refuse it if not an ASV.

You have medical issues causing centrals, you are, or were, also dealing with altitude causing CA. You need to bring it to your doctor's attention immediately. You need to highlight all the failures of PAP treatment, you need to discuss medical issues as cause, and you need to request that titration with ASV pressure sets. Very basically, you need to tell a doctor everything in this thread.

Understand what I say next, is you want ASV, I'm not telling you to lie whatsoever, but you are only going to mention negatives, the failure of PAP, CA all the time, all symptoms and complaints. There's no positive to mention in your situation, none. If they hear any positive thing, it may be misunderstood as the therapy being successful. It's not. You need to treat CA with ASV.
Mask Primer

Positional Apnea

INFORMATION ON APNEA BOARD FORUMS OR ON APNEABOARD.COM SHOULD NOT BE CONSIDERED MEDICAL ADVICE. ALWAYS SEEK THE ADVICE OF A PHYSICIAN BEFORE SEEKING TREATMENT FOR MEDICAL CONDITIONS, INCLUDING SLEEP APNEA. INFORMATION POSTED ON THE APNEA BOARD WEBSITE AND FORUMS ARE PERSONAL OPINION ONLY AND NOT NECESSARILY A STATEMENT OF FACT.
Post Reply Post Reply
#5
RE: CSA and Diet? your thoughts/experience please.
For a sleep test i suggest SleepTest #1 and ask for the Type 2 test. A type 2 test is very similar to an inlab test but it is at home, unattended, and without a PAP machine.
Talk to Jason about your issues first. This test should differentiate between Central and Obstructive Apneas. If you go this route Jason will go over the results with you. He does not go through insurance so you should get a "Prescription" for a Type 2 Home Study Sleep Test from your doctor to justify it to your insurance.

ASV. read this. http://www.apneaboard.com/wiki/index.php...P_Machines

I'm going to suggest that you post the Sleep Test(s) that you have already had.

You have had enough going on that I would prefer to see the results of a good sleep test such as the Type 2 mentioned above. I believe that you have had the much less robust Type 3 Sleep test. Guiding you going forward will be much easier with solid data to base it on. This test cannot say the diet works, but it can state unequivocably the current state of your apnea without a machine.
Post Reply Post Reply
#6
RE: CSA and Diet? your thoughts/experience please.
Congrats on your LCHF food plan change and the good results. I do not have a report for myself on LCHF and sleep apnea, but the diet almost completely eliminated migraines and optical migraines for me.

I wish you ever improving health.
====
Am caring for nonagenarian parents:  one uses a ResMed Airsense 11, and the other a ResMed Astral 150, full face masks, oxygen, humidifiers, modems.

Anyone else caring for very elderly loved ones?
Post Reply Post Reply
#7
RE: CSA and Diet? your thoughts/experience please.
This is just speculation, but once we get diagnosed with OSA, CSA, etc. we tend to think that's the ONLY thing that can be affecting our sleep. So if you have a bad sleep, just blame the apnea. But there's really so many other variables at play for quality of sleep (ie diet, exercise, stress, screen time, etc).

Great job on finding a diet that works for you and it sounds like it's allowing you to have more restful peace of mind and sleep. Just still keep an eye on the centrals and doing a home study as Gideon suggested is a good option.
Post Reply Post Reply
#8
RE: CSA and Diet? your thoughts/experience please.
I'm in agreement with Gideon's suggestion for the home study of better grade, higher level test.

Best to ya and keep us updated. Ask us you need help with anything.
Mask Primer

Positional Apnea

INFORMATION ON APNEA BOARD FORUMS OR ON APNEABOARD.COM SHOULD NOT BE CONSIDERED MEDICAL ADVICE. ALWAYS SEEK THE ADVICE OF A PHYSICIAN BEFORE SEEKING TREATMENT FOR MEDICAL CONDITIONS, INCLUDING SLEEP APNEA. INFORMATION POSTED ON THE APNEA BOARD WEBSITE AND FORUMS ARE PERSONAL OPINION ONLY AND NOT NECESSARILY A STATEMENT OF FACT.
Post Reply Post Reply


Possibly Related Threads...
Thread Author Replies Views Last Post
  F&P Solo Mask: Thoughts and Tips, Please LuminousOne 3 249 12-01-2024, 08:46 AM
Last Post: WallyPepper
  Phrenic nerve stimulator thoughts? EdElliott 13 1,363 11-15-2024, 08:46 AM
Last Post: MaxxtheDog
  New CPAP user, surprisingly great experience with Lofta Schnoozer 2 411 11-01-2024, 01:37 PM
Last Post: Schnoozer
  Switched from ASV to Bilevel, Odd Cheyne Stokes Respiration Patterns, Any Thoughts? LennySleeps 4 372 10-26-2024, 02:57 PM
Last Post: katbrat
  ac123 Treatment Thoughts/Help ac123 25 1,881 10-23-2024, 12:47 PM
Last Post: ac123
Question [Treatment] 5 years no relief, would appreciate thoughts FinnianWhitefir 0 249 10-20-2024, 07:37 PM
Last Post: FinnianWhitefir
  What was your experience fighting mouth leaks? PersonInNY 32 2,004 10-05-2024, 11:19 AM
Last Post: NewlyDiagnosed


New Posts   Today's Posts


About Apnea Board

Apnea Board is an educational web site designed to empower Sleep Apnea patients.