Story of Spstriken

Sorry man I have these issues too. As well as many other problems. Body does not react well to pro kidney foods /activities. Its very difficult. Insulin resistance can also cause a lot of these issues which I also believe many of us have. Very dry mouth dark and foamy excessive urination especially during the night.

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Now when I recall, I see my very first symptoms after starting SP were
1- Diarrhoea and gut issues.
2- Excessive watery urination. When I say excessive it does not mean frequent but with large volume more than my water intake. I was peering and peeing. My hands and body was going dryer and dryer.
3- Breaths with foul smell. I still get it back time to time. I never had this.
4- Waking up in the morning with bitter taste.
It looks like I have got all the symptoms already, but numbers for damage started showing up since 2012.
When I search I find if you have above normal vasopressin level and yet urinating a lot (watery) then more likely it is kidney issue. Your kidneys are failing to concentrate urine and your brain is pumping out more and more vasopressin.

NOTE: * Please do not get alarmed. I do not mean everyone who took Fin/SP has kidney issues. I have not seen many stories about kidney damage after using Fin/SP. Maybe I am the only one but it is better to check your kidney function and vasopressin level.*

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I have the same issues I piss absolute loads also I have times of the day/night when I have the sudden urge to pee loads and they correlate with start and peak of thr cortisol and testosterone cycles. Urine is pungent smelling. Skin is very dry peeling on scalp palms and scaly elsewhere.
Urine output exceeds water intake.
My Vasopressin levels mostly normal.
Sorry I hope I’m not muddying the waters.
NB Gut and digestive issues are a huge problem for me too

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I must pee every hour or two, day and night. Wife says it is the worst smelling pee, too.

Doctor is watching my kidney numbers, so he must see something worrisome if not yet alarming. FYI. Jim

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I have shared my lab values here. Please get your tests/labs done and then share. Do not make assumptions/speculation as this might be depressing for some people.

I am also a frequent urinator but not in the noon/evenings/over night. My urine spells come in the morning, also started with the length of the SP crash. It doesn’t really smell though. Its gotten somewhat better over the months, just something I deal with now as embarrassing as it can be.