Nap 50s steroids

Hi girls. I know this thread was last year but thought I would pop in anyway just in case. I too have HIGH cortisol levels and have struggled with this for over 12 years. Yep 12! Count them…. physical anxiety with all the nasty symptoms and am currently battling it again. With that said, in my research about this problem, I came across Dr. Joseph Mercolas website. He did an article on a test called the DUTCH test. It tests ALL the hormones connected to your adrenals AND their metabolites! I have done many saliva tests in the past but this one give you so much more about why they could be high. In Mercolas article he interviewed Dr. Mark Newman creator of the test. What sold me on this test was the example he gave of a gal that had the test and they found she had high cortisol, and if it was the saliva test they would have administered Seri-Phos to lower the levels because all you see on the saliva test is measurement of cortisol not metabolites. So on her test it showed her metabolites were low! Throwing seriphos at them was not the solution. It was an imbalance. Not that she was producing too much but the cortisol she had wasn’t leaving her body. Anyway, I thought it was worth the money to have it checked out. I bought the test online (don’t have to have a doc to order it and you get off using Mercolas name) Anyway, the results for me was amazing. ALL my hormones that they tested were off the charts!!! I now know I have PCOS (not known before) I have been estrogen dominant all my life even with oophorectomy. So, just thought you might like to know about another option for testing. Not sure how I’m going to get “fixed”. that’s another story. I think Dr. Jonathan Wright does his own version the test too. You can google Mercola and search on his sight for DUTCH test and get discount or you can google DUTCH test on the net. It is a urine test and the turn around time is about 2 weeks.

The weight gain, caused by having years of see-sawing between starvation when bingeing on meth and then binge eating when there is no meth around. Meth use has wrecked his ability to regulate many of his normal functions. He now never feels full after eating. He once ate a $300 food shop in a day and then went out that night for hamburgers. The resulting spikes in blood sugar levels make him vulnerable to infections, as do the periods of no nutrition when bingeing. This means that any cuts, pimples or ingrown hairs can rapidly turn to large, painful abscesses.

2. Fosfomycin (PO)
Bactericidal agent that is excreted into the urine and inhibits cell wall synthesis by interfering with peptidoglycan synthesis.
Spectrum: Broad spectrum vs Gram positive including MRSA, VRE; Gram negative including Pseudomonas and some ESBL’s . 
Used for: Uncomplicated urinary tract infections in women, especially in those with history of resistant bugs.  Given as a one-time mega-dose of 3 g (excreted into urine and achieves high levels there for several days.   Sometimes used for complicated UTI’s in males with resistant pathogens (3 g PO q3 days x several doses), although this is an off-label use.

This is awful,and you need to understand that it’s not you. My belief from what you described is there is real damage to you cord, muscles, and nerves at the location. I personally went in for a C4-5 bone graft, and was woke with a C4,5,6,7 cage installation, 2 different neck cuts to access the site, and in pain as if the surgery was still being 4th day of refusing to leave,unable too. On 5th day I was able to stand and walk loaded with alot of IV pain discharged me that evening, 9 days later I barely made it in for visit,4 weeks later i found myself being dismissed when unable to walk, speak, lose control of my urine. In short it was the beginning of nothing else I can do, to i won’t see you again, and had me removed using the police. This was back in Dec3,2013, now I’ve got narrowing of the spinal cord at every level of the c2,3,4,7, now same at the L1,2,3,4,and S1. Since this I’ve been provoked to no pain meds, always u need pain pump,i injections, and suffering until insane. If I had the chance to go back in time, I’d went to assisted living where they had to manage the pain, and rest until I got better. In short I went to Florida, done nothing but rest for 7 months before I got to this point of variable pain. They are slow killing is, and don’t care what you go through as they dont even remember you doctor visits. It was hard to except. My point is, Everytime I listen to them instead of my body, I was just a pitiful mess. You need to get with the best spine people and pray they can fix it, but don’t worry about getting back to normal or even the simplistic things as it will take you back to hell and it takes longer Everytime you have flare it up. I laid like a vegetable for 18 months before I figured it out. Now I’m in bad shape and they are offering only injections, I’m thinking really hard, shame they are not made to get you better. This is what’s going on with society today, they’ll have to answer one day. But you make sure your not stubborn like I was and demand treatment it takes and the proper care. I’m praying for you, and I hope we get this country on the right track again as well as the compassion for others comes back

Nap 50s steroids

nap 50s steroids

This is awful,and you need to understand that it’s not you. My belief from what you described is there is real damage to you cord, muscles, and nerves at the location. I personally went in for a C4-5 bone graft, and was woke with a C4,5,6,7 cage installation, 2 different neck cuts to access the site, and in pain as if the surgery was still being 4th day of refusing to leave,unable too. On 5th day I was able to stand and walk loaded with alot of IV pain discharged me that evening, 9 days later I barely made it in for visit,4 weeks later i found myself being dismissed when unable to walk, speak, lose control of my urine. In short it was the beginning of nothing else I can do, to i won’t see you again, and had me removed using the police. This was back in Dec3,2013, now I’ve got narrowing of the spinal cord at every level of the c2,3,4,7, now same at the L1,2,3,4,and S1. Since this I’ve been provoked to no pain meds, always u need pain pump,i injections, and suffering until insane. If I had the chance to go back in time, I’d went to assisted living where they had to manage the pain, and rest until I got better. In short I went to Florida, done nothing but rest for 7 months before I got to this point of variable pain. They are slow killing is, and don’t care what you go through as they dont even remember you doctor visits. It was hard to except. My point is, Everytime I listen to them instead of my body, I was just a pitiful mess. You need to get with the best spine people and pray they can fix it, but don’t worry about getting back to normal or even the simplistic things as it will take you back to hell and it takes longer Everytime you have flare it up. I laid like a vegetable for 18 months before I figured it out. Now I’m in bad shape and they are offering only injections, I’m thinking really hard, shame they are not made to get you better. This is what’s going on with society today, they’ll have to answer one day. But you make sure your not stubborn like I was and demand treatment it takes and the proper care. I’m praying for you, and I hope we get this country on the right track again as well as the compassion for others comes back

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nap 50s steroids