Guest guest Posted September 15, 2010 Report Share Posted September 15, 2010 Are you referring to KPU like what Dr. Klinghardt refers to or is this something else? please do share your research so I may ask my ND? I think the nausea for me was more like pms nausea because my breasts were tender also. But I am being treated for KPU. Thank you! > > > > > Hi Again > > > > So I had a total hysterectomy in 2001 for stage 1 ovarian cancer and > Endometriosis. Then I had what I thought was a hard time with bioidentical > HRT, but now know it was the LD. I then had a doctor who gave me the up and > coming " pellets " of hormones implanted in my hip. He never 1 time in 5 > years > took my hormone levels even though I kept asking. He said he didnt need to > because they would only release as much as my body needed. I had no money > and no insurance to go elsewhere so I trusted he knew what he was doing. > The > pellets were supposed to last 4-6 months but I went in every month with > what > I though were menopause symptoms. I now know they were Bart symptoms. He > kept giving me more pellets every month. > > > > When I started having low thyroid symptoms and adrenal issues I begged > him > to please draw all the specialty thyroid tests. He did and I was Hypo with > reverse T3 syndrome. Armed with this diagnosis I found a specialist and > spent my life saving seeing them for 3 years. They are the ones who missed > the lyme diagnosis even though they also see Lyme patients as > Endocrinologists who specialize in Bio Hormones/Endocrine and Auto Immune > diseases. When they drew my hormone levels my estrogen was 2,487 and normal > range is 70-200. It took me 11 months to crash off of all that estrogen and > testosterone. > > > > I was then terrified to take any hormones because when i did my head > would > hurt and I felt like poison was running through my veins (It was the LD > reacting to it). So fast forward to today since my LD diagnosis. My LLND > wanted me to take a very small dose to help my body be more stable going > thorugh this. So I got the creams and I tried the tiny bit night before > last > and my Bart symptoms flared real bad and I was terrified. Does anyone know > if this might settle down as my body adjusts to the chemical change? Will > it > make more bugs? I hear such conflicting reports as to weather we need them > or not. I had been HRT free for 18 months before this. Sorry so long I am > just a little confused. Thank you for any advice. > > > > Blessings > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 16, 2010 Report Share Posted September 16, 2010 KPU and Porphyria are separate and yet I believe they would both be considered metabolic disease. The testing is similar in that you have to protect the urine from light. Dr. K used a lab in France to test my daughter. Some of the integrated Dr.s have been testing for Porphyria for quite some time but mostly to determine Mercury toxicity. I believe the Porphyria is much more significant than just mercury although mercury is devastating to our health. There are 8 different types and getting the correct diagnosis is difficult. Our LLMDs are just starting to put their heads together on this.The lists of contraindicated drugs can be googled .....but getting a clear diagnosis is tricky. On Wed, Sep 15, 2010 at 2:40 PM, MG <goddess_mystic@...> wrote: > > > > Are you referring to KPU like what Dr. Klinghardt refers to or is this > something else? please do share your research so I may ask my ND? I think > the nausea for me was more like pms nausea because my breasts were tender > also. But I am being treated for KPU. Thank you! > > > > > > > > > > > > Hi Again > > > > > > So I had a total hysterectomy in 2001 for stage 1 ovarian cancer and > > Endometriosis. Then I had what I thought was a hard time with > bioidentical > > HRT, but now know it was the LD. I then had a doctor who gave me the up > and > > coming " pellets " of hormones implanted in my hip. He never 1 time in 5 > > years > > took my hormone levels even though I kept asking. He said he didnt need > to > > because they would only release as much as my body needed. I had no money > > and no insurance to go elsewhere so I trusted he knew what he was doing. > > The > > pellets were supposed to last 4-6 months but I went in every month with > > what > > I though were menopause symptoms. I now know they were Bart symptoms. He > > kept giving me more pellets every month. > > > > > > When I started having low thyroid symptoms and adrenal issues I begged > > him > > to please draw all the specialty thyroid tests. He did and I was Hypo > with > > reverse T3 syndrome. Armed with this diagnosis I found a specialist and > > spent my life saving seeing them for 3 years. They are the ones who > missed > > the lyme diagnosis even though they also see Lyme patients as > > Endocrinologists who specialize in Bio Hormones/Endocrine and Auto Immune > > diseases. When they drew my hormone levels my estrogen was 2,487 and > normal > > range is 70-200. It took me 11 months to crash off of all that estrogen > and > > testosterone. > > > > > > I was then terrified to take any hormones because when i did my head > > would > > hurt and I felt like poison was running through my veins (It was the LD > > reacting to it). So fast forward to today since my LD diagnosis. My LLND > > wanted me to take a very small dose to help my body be more stable going > > thorugh this. So I got the creams and I tried the tiny bit night before > > last > > and my Bart symptoms flared real bad and I was terrified. Does anyone > know > > if this might settle down as my body adjusts to the chemical change? Will > > it > > make more bugs? I hear such conflicting reports as to weather we need > them > > or not. I had been HRT free for 18 months before this. Sorry so long I am > > just a little confused. Thank you for any advice. > > > > > > Blessings > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 16, 2010 Report Share Posted September 16, 2010 Please, please, please, delete posts you are not responding to!! Please. I am on the verge of cancelling my membership because the digests are so long (can't get them on a page without tiny print)). Is this a problem for anyone else or is it just me having a problem? jo Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 17, 2010 Report Share Posted September 17, 2010 ? [ ] Re: HRT and LD...To B Please, please, please, delete posts you are not responding to!! Please. I am on the verge of cancelling my membership because the digests are so long (can't get them on a page without tiny print)). Is this a problem for anyone else or is it just me having a problem? jo Quote Link to comment Share on other sites More sharing options...
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