my sleep habits are the same after DX and 4 years of treatments. I sleep on a APAP machine ( have for 20+ years ), so my sleep quality is monitored in detail. I sleep with a AHI of .8 or so ( like a baby ) before and after cancer DX. My sleep is 6 hours at night with daytime naps due to exhaustion and tiredness caused by ADT. I take 10mg melatonin before bedtime every night.
I go to bed around 11Pm & sleep soundly untill 6 AM & take 20mg Melatonin every second or third day because it makes me have daily naps, which may be ok for some.
A sound sleep is important to reduce stress I believe & Melatonin certainly helps.
Waking up almost every night but normally fell asleep quickly again. I take 10 mg Melatonin at bed time which is between 22.15 - 23.00 pm. Wake up between 6 - 7.30 am. I believe in good sleep to give my body enough time to regenerate and repair. I also adopted my eating habit. I’m on time restricted eating, only eat between 12.00 - 1.00 and 6.00 - 7.00 pm.
I am trying to improve my sleep by reducing the light in my bedroom. Scientific studies show that dim light during sleep can increase obesity and cancer in mice. See this article, which says dim light at night sleep increases diabetes, obesity and hypertension.
I also use plugin nightlights and use room lights sparingly during trips to the bathroom, and I close my bedroom door while sleeping. I also have no television or computer monitor in my bedroom. After doing this for a month I began to have more frequent vivid dreams, which I take as evidence of deeper sleep, although I admit the dreams do at times scare me to awaken.
I cannot say much about deep sleep and advanced prostate cancer, except that my PSA has been consistent at <0.1 and metastases seem to be reduced, . Weight loss seems impossible. I don't have diabetes. This experiment has not clearly benefitted me in any obvious way other than the vivid dreams, but I do believe that deeper sleep helps the body's immunity..
P.S. My blood glucose levels have come down consistently to barely normal from above normal, and blood pressure has come down slightly during the past few months of the experiment. I cannot say these are improvements due to less dim light while sleeping. The blood glucose has to do with timing of blood tests. Reduced blood pressure is not very significantly lower, but I believe it is caused by my medicatiions.. I do take a betablocker which keeps my heart rate down.
Yes, I too, have researched light at night and how it affects sleep.
The one other thing I find helpful, whether or not it is advocated for PC and sleep issues, is Not using a computer, phone or tv a couple hours before you want to sleep.
I have never needed a lot of sleep - no more than 5 to 6 hours/night. Since I've had an enlarged prostate and PCa, I now am lucky to sleep for more than 1 hour at a time before needing to do a pee. I generally get back to sleep reasonably quickly but sometimes end up lying awake for a couple hours getting up to pee once or twice again during that time. I'm usually up by 7am and estimate I get 4 to 5 hours sleep max most nights, but I seem to be functioning OK on this. I do sometimes have an afternoon nap for an hour or so if particularly tired.
my father who has been recently diagnosed at 65 years old has slept only 4 hours a night since he was 20 years old. He’s in a super deep sleep for 4 hours a day and then he’s up and about. Doesn’t force it.. it’s just when his body says “I’ve had enough sleep”
226PSA. Bone scan and CT scan complete. These scans supposedly ruled out bone Mets and organ spread. Some lymph nodes just outside prostate are swollen tho so possible spread to those
Biopsy Nov 3rd with discussion appointment Nov 23rd. So I am super scared this wait will cause further spread. I’m terrified but hanging in there to see what the full diagnosis is and I just pray to god that it will all work out
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