Guest guest Posted January 31, 2003 Report Share Posted January 31, 2003 What type Testosterone....gel or injections? Have you had your T levels measured? If you are on gel, particularly AndroGel...not everyone absorbs well. You should have felt some improvement after three months. I would suggest you have T measured. Good luck, OR eon Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 1, 2003 Report Share Posted February 1, 2003 The first time I used TRT I got an injection and it started working in about a week. Then I switched to 5g Androgel and it didn't work. My total testosterone was 542 with Androgel. I stopped taking Androgel and a few months later the symptoms got much worse (even though another T test said my total was 501) so I restarted TRT with 300mg cypionate injections for the first 2 months and then I switched again to Androgel and Im taking 5g a day, sometimes 10g because I got some packets left over from before. What confuses me is that the injections worked rapidly the first time and the second time they did nothing. > What type Testosterone....gel or injections? Have you had your T levels > measured? > If you are on gel, particularly AndroGel...not everyone absorbs well. You > should have felt some improvement after three months. > > I would suggest you have T measured. > > Good luck, > > OR eon Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 1, 2003 Report Share Posted February 1, 2003 I have been on the patch for almost three months, and I feel the same way you do. It was particulary bad after the first month. Depressed, no sex drive, no erections, lose of muscle mass, testiles shrinking up and painful. I started taking zinc and Chrysin like Dr Shippen says to and it helped a little but not that much. I have been struggling to get my endo to re evaluate my treatment with no luck, so I made an appointment with another endo. Now I have to wait my turn to get in to see her. Let us know how your doing SB Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 1, 2003 Report Share Posted February 1, 2003 Hi mikcd, You need to go to your endo and get your levels checked. You may need a higher dose or different method of testosterone replacement that suits your body. > I've been on TRT for 3 months and my symptoms have become worse. > Does this mean that TRT failed or do I have to wait longer? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 5, 2005 Report Share Posted February 5, 2005 Whilst its not very helpful the simle is IT DEPENDS! Depends on why the problem in the first place, diet all sorts. I beleive my sons issues were induced by toxic heavy metals, I don;t expect his yeast issues to be gone until the metals are - we have been at this 4 years so far............. You should see behavioural and physical improvements with yeast and enzyme treatments over time - have you see any yet? Mandi in UK wrote this message earlier this week and no response. I would like to know how long do you do the enzymes and probiotics to fight the yeast....3 months, 6 months, forever?? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2005 Report Share Posted February 6, 2005 > I wrote this message earlier this week and no response. I would > like to know how long do you do the enzymes and probiotics to fight > the yeast....3 months, 6 months, forever?? It depends on how entrenched the yeast is, what your child eats, and how much metal is in his body. For many kids, you can't entirely control the yeast until the diet is " clean " of sugars and most carbs, and/or you chelate to remove the metals. Depending on what yeast killer you use and how bad the yeast is, it can take anywhere from a week to over 6 months to get rid of it. But then it will just come back if you don't have a maintenance protocol. Most people use probiotics as maintenance. Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2007 Report Share Posted February 25, 2007 In a message dated 25/02/2007 14:29:30 GMT Standard Time, Ladyshrink111@... writes: Is different for all kids, mostly by 5-7 rounds completed, but for us was the third day of the first round, although I'm certain it wasn't due to excreting any significant amount of metals (how could it be?) but more the improvement was probably due to the cysteine in the chelators. I would be highly suspicious if someone doesn't see anything by 10 rounds. >>took us 20 to see anything good, glad I didn;t give up too early Mandi in UK Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2007 Report Share Posted February 25, 2007 Is different for all kids, mostly by 5-7 rounds completed, but for us was the third day of the first round, although I'm certain it wasn't due to excreting any significant amount of metals (how could it be?) but more the improvement was probably due to the cysteine in the chelators. I would be highly suspicious if someone doesn't see anything by 10 rounds. [ ] How long? When have you all seen gains after beginning chelation? Curious.... A. --------------------------------- Don't pick lemons. See all the new 2007 cars at Autos. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2007 Report Share Posted February 25, 2007 Our son was diagosed as severely autistic at 6 years old. He was hyperlexic but could not follow simple verbal commands. He had numerous temper tantrums. Most of what he said was scripting. He couln't stand being with a group of people without keeping his hands over his ears. is now 11. He now has lost his hyperlexia, but understands what he reads. He is very social, although what he says is not always appropriate. He is doing the aBeka school curriculum at grade level with mostly 'A' work. He still stims and perseverates at times. He brings a smile to my face when he is mischievous, because I feel that is the normal little boy trying to appear. We have finished 116 rounds now, and I see a little more progress with each round. He still isn't normal, but he still meets the counting rules. I am so thankful for Andy and this protocol, because they have given me hope when noone else could. Perhaps, we as parents need to enjoy our children as they are and patiently watch them evolve. Warm regards, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2007 Report Share Posted February 25, 2007 Thank you, , for sharing your wonderful story. Rene > We have finished 116 rounds now, and I see a little more progress > with each round. He still isn't normal, but he still meets the > counting rules. I am so thankful for Andy and this protocol, because > they have given me hope when noone else could. Perhaps, we as > parents need to enjoy our children as they are and patiently watch > them evolve. > > Warm regards, > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 26, 2007 Report Share Posted February 26, 2007 Wow, , this is great! > We have finished 116 rounds now, and I see a little more progress > with each round. He still isn't normal, but he still meets the > counting rules. I am so thankful for Andy and this protocol, because > they have given me hope when noone else could. Perhaps, we as > parents need to enjoy our children as they are and patiently watch > them evolve. > > Warm regards, > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 28, 2007 Report Share Posted July 28, 2007 > > I was diagnosed with M.S. 10 years ago. I have only taken natural vitamins & herbs. No copaxone or avonex. The side effects of these sounded worse than what I was experiencing. I have just gone back to my neurologist after 10 years and printed off information about LDN and I believe she is going to perscribe this for me. I need to know where & how to get a perscription filled & How Long before seeing results? Expecting & excited about starting this. > ========== H, Read thoroughly the LDN website at www.ldninfo.org and if you like, Aletha can email you a welcome packet with all sorts of links to read. LDN's main purpose is to halt disease progression, approximately 2/3 of people who go on LDN might see some symptom improvement, if you get symptom improvement on LDN then consider that an added plus. Give LDN 9 months to a year trial to really start halting disease progression. Try using one of the relable compounding pharmacies listed on the LDN website or give one of them a call and ask questions. /Bren, LDN user 4 yrs for PRMS. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2009 Report Share Posted September 7, 2009 No you need to know where your levels are at with the does your taking. If your doing .25 mgs every 3 days and your levels come back at say 28 you need to do the .25 mgs every 2 days it's best to be at 20 pg/ml. If your levels come back below 20 and you have good hard night time and morning wood keep on the dose you taking. But if your lowre and have no wood you need to stop taking it until wood comes back then that day go back on it but do less. Co-Moderator Phil > From: Kipp Kruse <kckruse@...> > Subject: how long? > > Date: Sunday, September 6, 2009, 10:59 PM > should I be off armidex before I get > my E2 tested to get an accurate measurement of my true E2 > reading on my current testosterone dosage without taking > armidex? > > 48 hours enough? longer???? > > thanks > > > > > > > > > ------------------------------------ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 6, 2010 Report Share Posted July 6, 2010 My son is 6 months old today, he has had his helmet a little over a week now. How long would any of you guess he might have to wear it? They said anywhere from 8 weeks to 6 months. I hope it's not 6 months, but if it is, it is. I know a baby that got his at 6 mths and he graduated at 8 mths, i hope that is us too. Quote Link to comment Share on other sites More sharing options...
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