LoneStar wrote:Have you had your thyroid checked? Not just the TSH, but a complete thyroid panel including T3, T4, free T3/4, etc.? And have your doctors checked you for adrenal gland fatigue with a saliva cortisol test? How are your vitamin D3 levels? If there is a functional medicine specialist in your area, you should consider seeing them.
I've had it checked several times but I don't know what all was checked. I did have my adrenal glands checked I think. Is that where you give a blood sample, go back the next day after taking a pill and give another sample? I have such a bad memory. Everything came out fine in all of that.
Bugdude wrote:My thoughts are with such a high pressure, I have to wonder if you're getting mouth leakage with your nasal mask. I know you say you believe you don't, but it's easy to not notice or realise you're mouth is farting at night.
Try getting a loan of a FF mask: you've got nothing to lose.
My ex has a FF mask he isn't using. I'm working with him to see if I can borrow it.
Pugsy wrote:Welcome to the forum?
Do you have the software to use with your new machine to make sure that at least on paper that things are at least optimal as far as your therapy goes? Leak line and numbers, if elevated, might indicate mouth breathing or other leaks great enough to impact therapy.
Using the software you can spot any areas of therapy which might need improvement. If all the data looks good on paper then we do have to look at other possible contributing factors to not feeling the good numbers like sleep fragmentation, hours of sleep, pain, med and other health issues which have already been mentioned.
I had a problem with sleep fragmentation due to pain. I had great numbers on my software reports but I knew I woke up many, many times during the night due to pain. Anything that messes with sleep will mess with how we feel the next day. So have you used the software to make sure the data looks good on paper and nothing needs work?
I just downloaded the SleepyHead software last week but I didn't really understand much of it. I plan to ask more in a separate question when I get a chance.
kteague wrote:What is being done about your periodic limb movement disorder? Have they done iron studies, magnesium level - - - anything???? If your PLMD is anything like what I've suffered, you have my sympathy. My guess is treating your limb movements along with therapeutic cpap treatment would give you a sizeable portion of your life back.
I'm taking Neurotin for the pain in my legs but I don't think it helps the PLMD. I'm thinking it is related to the high dose of Effexor XR that I'm on. I seem to remember reading something that it can cause twitches like this. I've had them for so long and been on Effexor for so long too that I don't hardly notice them anymore. But I do think my neuro was going to wait and see how the new pressures did for my sleepiness first and then when I see him in Feb., he would address the PLMD.