FEARSeve­ral years ago, a large per­cen­tage of thy­roid patients on yahoo groups like NTH were figu­ring out that they had adre­nal fati­gue, aka low cor­ti­sol, from years of adre­nals wor­king over­time due to the ina­de­quate TSH lab test, or being on the lousy T4-only medi­ca­tions like Synth­roid, Levoxyl, levothy­ro­xine, Eltro­xin, etc.

Not only does low cor­ti­sol keep desic­ca­ted thy­roid from wor­king well, it also cau­ses all sorts of angst with para­noia, depres­sion, anxiety, easy anger, sen­si­ti­vity to light and/or sounds, rec­lu­si­ve­ness, sleep issues and more.

First, patients dis­co­ve­red the impor­tance of using the 24 hour adre­nal saliva test rather than blood or urine. When low cor­ti­sol was con­fir­med, the treat­ment was using cor­ti­sol, aka hydro­cor­ti­sone, to give them­sel­ves back what their adre­nals were not, to allow thy­roid hor­mo­nes to reach the cells, and to give the poo­ped out adre­nals a rest.

And suc­cess was achie­ved! When all other issues were dis­co­ve­red and trea­ted, patients were finally able to heal their adre­nals with cor­ti­sol use, wean off, and be suc­cess­ful in their con­ti­nued treat­ment with desic­ca­ted thy­roid! That suc­cess con­ti­nues today!

Yet in spite of clear suc­cess in the treat­ment of low cor­ti­sol with sup­ple­men­tal cor­ti­sol in the correct amount for each indi­vi­dual (which can range from 15 to 40 mg gene­rally – men often need the higher end), as well as exce­llent books on the sub­ject by Wil­son, Peat­field, Jef­fries and the STTM book, patients like RD below still encoun­ter doc­tors who fill their minds with all sorts of fear and warnings:

I bought your book and later on I dis­co­ve­red your web­site which are both great. They are a superb source of infor­ma­tion and sup­port for thy­roid and adre­nal fati­gue suf­fe­rers. Thank you so much!

Per­so­nally I got adre­nal fati­gue by a sus­tai­ned lack of sleep for seve­ral years (crying babies).  I found a doc­tor who presc­ri­bed Hydro­cor­ti­sone (17.5 mg/day, 5 – 5-5 – 2.5), Flu­dro­cor­ti­sone, DHEA and Tes­tos­te­rone. Symp­toms disap­pea­red in about 2 weeks.

A first attempt to wean off after 6 months made some serious symp­toms reap­pear very quickly, so I retur­ned to the ori­gi­nal dose.

It is very stress­ful that many esta­blished doc­tors (our family doc­tor, and my wife’s thyroid-endocrinologist) are sca­ring me like hell that I am taking HC. They are saying I am des­tro­ying my body and I will never suc­ceed in wea­ning off HC.

My wife is a T4-only thyroid-patient with low-cortisol symp­toms. She also has been sca­red about des­si­ca­ted thy­roid and HC. Rea­ding your book I was howe­ver con­vin­ced she could bene­fit a lot from a bet­ter treatment…

Keep up the good work, as patients we are really left alone in the dark by our doctors…

And unfor­tu­na­tely, it’s true. Thy­roid and adre­nal patients are left in the dark by many doc­tors about a variety of issues rela­ted to bet­ter thy­roid treat­ment, adre­nal issues, low ferri­tin, and more.  So here’s where you can read more, and in turn, take this impor­tant infor­ma­tion into your doc­tors offices:

  • All about the pro­blem of adre­nal fatigue
  • How to treat
  • Symp­toms of having an adre­nal problem
  • The STTM book, which not only has more detail, but can be taken right into the doctor’s office
  • Talk to other patients, inc­lu­ding a group tar­ge­ted for adre­nal fatigue

*********************************************************

Dr.JohnCLoweIf you mis­sed the exce­llent Part 2 with researcher Dr. John C. Lowe last Thurs­day eve­nings, you can lis­ten to the recor­ding, as well as sign up to be a Follo­wer of the Thy­roid Patient Com­mu­nity Call, here.


  • Want to keep track of these “fringe web­site” blog posts? ;-) Curious what’s on Janie’s mind? Use the noti­fi­ca­tion on the lower left of the links, called a News­let­ter, or an RSS Feed.
  • The extre­mely hip and sophis­ti­ca­ted STTM t-shirts are half price! Great BUMPER STICKERS, too. Spread the word – YOU may make a dif­fe­rence in someone’s life.
  • Check out the patient-to-patient book with even more detail (and which doc­tors seem to res­pect more than websites).
  • Need to unders­tand all your best options for thy­roid treat­ment? Go here.
  • Keep infor­med of each live Thy­roid Patient Com­mu­nity Call on Talkshoe by sig­ning up as a follo­wer.

18 Responses to “A guy’s story: scaring the hell out of him about being on HC cortisol!”

  1. Abby said:

    Jan 17, 10 at 10:55 am

    I don’t yet have ‘stu­dies’ on my per­so­nal use of long-term HC.

    What I do know is that living a life on tan­ked out adre­nals is not a life worth living, for me.

    For me, life on HC, no mat­ter what kind of ‘scary’ things can hap­pen because of it (and I want some evi­dence that I’m ‘rui­ning’ my body), is still pre­fe­ra­ble to living the life I lived prior to HC.

    What kind of life is it when I’m too exhaus­ted to work, so much anxiety that I need to be on psychia­tric drugs that come with their own set of side effects and further deplete adre­nal func­tion (and what about the pro­ven side effect of the dar­ned drugs: sui­ci­da­lity, isn’t HC pre­fe­ra­ble to THAT?, and the myriad symp­toms rela­ted to deple­ted adrenals.

    Now, on HC, no need for psych drugs, energy to do the things I need to do, and if in the long run HC will have shor­te­ned my life (which someone has yet to prove to me) at least I will have lived these years qualitatively.

  2. Renee said:

    Jan 17, 10 at 11:51 am

    So I have hypo for about 5 yrs now and suf­fe­red from adre­nal fati­gue as well. I was told the same nega­ti­ves about taking cor­ti­sone, and quite frankly I side with the drs. I took other adap­to­gens and cer­tain her­bal sup­ple­ments in a pro­duct line by NeuroScience-which are presc­ri­bed in tan­dem based on saliva test panels every 4 months. My cor­ti­sol levels when I star­ted the the­rapy 2 yrs ago, were around 2 in AM, and 0 at bedtime-4 tests thru out the day-should have been around 10 – 11 in AM and 0 – 1 by bed­time. Right now my last panel after having taken the sup­ple­men­tal the­rapy for 1 yr and then a yr off, now my body has star­ted to remake cor­ti­sol on its own and now my AM levels are around 7 and 1 at bed­time. So I am get­ting there. Rho­diola rosea is one of the active ingre­dients in the adre­nal for­mula, and I think 5-HTP?-its called “Adre­cor”.
    But any­ways by balan­cing other neu­ro­trans­mit­ters, vita­mins, and hor­mo­nes affect your adre­nals as well, it is a very com­pli­ca­ted dance of che­mi­cals that I still dont unders­tand, but I know it took ALOT of patience and nap­ping and rea­ding online to even unders­tand and feel when my body feels good. I also have Meyer’s Cock­tail IV sup­ple­ment once a month, and that hel­ped repair them as well. I had an MRI to rule out cysts or tumors which all peo­ple should have done with this con­di­tion, it sho­wed nothing.
    My drs con­cern about HC was that by sup­ple­men­ting with hydro­cor­ti­sone straight out of the gate then you are in essence con­di­tio­ning your adre­nals to not bother to pro­duce any on their own, and over time you ren­der them use­less. And that adre­nals should not be con­si­de­red like hypothy­roid issues they dont func­tion the same way where you will always need to be on it. They can repair.
    My per­so­nal take is that I found when I got rid of stress-afterall they were coo­ked from yrs of stress and reduc­tion of nutrients in body used up to reco­ver from yrs of stress-well once you fix those imba­lan­ces which I did I feel I am repai­ring my body and feel about 70% bet­ter then when I star­ted 2 yrs ago. I am still married to a spe­cial variety of ***hole so that takes its toll, but even that is beco­ming a deal­brea­ker for my health so when that deci­sion is made I know I will be 95% bet­ter, right now I feel about 70% bet­ter since when I star­ted 2 yrs ago.
    I’m not saying I wouldn’t have taken hydro­cor­ti­sone, or he wouldn’t have presc­ri­bed it AT ALL, but we tried the natu­ral way first-that was our plan, and it slowly but surely is wor­king. I think its unwise in any area of health­care to just throw drugs at something when the body is capa­ble of hea­ling itself with the right modi­fi­ca­tions.
    I am more con­cer­ned though about peo­ple who dont have access to the same health­care I do & who dont even have a dr who belie­ves adre­nal fati­gue is a real con­di­tion, or who even do saliva tes­ting. If I did not have decent care to do the natu­ral route and the time to wait to heal on a natu­ral pro­gram then I’d pro­bably push for the Rx.
    Thats just my opi­nion I could be wrong.

  3. Darla said:

    Jan 17, 10 at 12:00 pm

    HC as well as Natu­reth­roid have saved my life, career and pos­sibly my marrage. I know I didn’t want to live with myself, why would anyone else?

    Without HC the Natu­reth­roid couldn’t work. The Synth­roid cer­tainly never wor­ked. My adre­nal func­tion was low all day long.

    Once had a doc tell me that I would have to be close to death in the hos­pi­tal before he would rx HC to me. Why in the world would I want to wait that long? Do something to pre­vent it NOW!!

  4. Kerry said:

    Jan 17, 10 at 12:10 pm

    I found a doc­tor I love. A doc­tor willing to presc­ribe desic­ca­ted thy­roid, HC, and other things most doc­tors won’t. It still ama­zes me when I go to other doc­tors (gyno, etc,) and they ask what presc­rip­tions you take and they freak. All my other doc­tors keep telling me that HC, DHEA and natu­ral desic­ca­ted are not the best options and that they don’t unders­tand why I would be taking them at all. The endo I went to before I found my doc told me that natu­ral desic­ca­ted would give me a heart attack. Hello! Half the stuff my doc has me on is ALSO used to help patients with heart pro­blems. I don’t unders­tand why there is such con­tro­versy over presc­rip­tions that most patients say have been ama­zing for them.

  5. Carrigon said:

    Jan 17, 10 at 2:09 pm

    All the docs I’ve been to con­ti­nue to deny the exis­tence of Adre­nal Fati­gue. And most of them don’t even know anything about Hashimoto’s. I went to one quack that told me Hashimoto’s is nothing more than inflam­ma­tion and I should take NSAIDS for it! None of these doc’s know anything.

    My current doc has me on Levothy­ro­xine because I had terri­ble pro­blems with the new Armour for­mu­la­tion. The Lev got my level down, but I can’t lose weight on it and in gene­ral don’t feel well on it. And still get the cold hands and feet and all that. I’m never well, and I think it’s because I’m being undertreated.

  6. Jan said:

    Jan 17, 10 at 3:20 pm

    After batt­ling adre­nal fati­gue since pro­bably my early 20’s I have found that doc­tors tend to base their “scare tac­tics” on the early days of using HC when it was given out for everything in very high doses and tou­ted as a miracle. Mind you this was long before I was born. Today, it seems the drugs of choice for adre­nal fati­gue are anti­de­pres­sants and anti-anxiety drugs. Pro­fi­ta­ble and they don’t lead to a cure. They keep you coming back for follow up presc­rip­tions and liver blood work and if you try to get off them.…the anxiety comes back triple-fold. Those drugs come with their own list of scary risks and side effects, like per­ma­nent liver damage..no worse than HC in my opinion…probably far worse. It’s simply misinformation!

  7. Maria said:

    Jan 17, 10 at 3:52 pm

    Armed with the infor­ma­tion that I had after rea­ding Janie’s book “Stop the Thy­roid Mad­ness”, and Mary’s “Living Well With Hypothy­roi­dism”, and seve­ral others sug­ges­ted by Janie (and seve­ral nights of no sleep) I con­fron­ted my Doc­tor. He finally sent me to a endoc­ri­no­lo­gist. Today I went for many blood test. He said my insu­rance will not pay for Natu­ral Thy­roid. But he’s willing to presc­ribe it.

    I have been on levoth­roid for many years. Have con­ti­nued with hypo symp­toms. Thanks Janie and all the others that have given me the cou­rage to say to my Doc­tor, YOU ARE WRONG, it is NOT in my head.
    Lets keep the pres­sure on them to lis­ten to us and to our symp­toms, not just Lab #‘s

  8. Margaret said:

    Jan 17, 10 at 5:33 pm

    The way I see it, use of HC to replace cor­ti­sol is just like repla­cing any other hor­mone that you might need. If you are lac­king, it needs to be repla­ced if you want to feel better.

  9. Abby said:

    Jan 17, 10 at 9:47 pm

    Renee, con­si­der your­self lucky! I am so glad it wor­ked for you!

  10. Jennifer said:

    Jan 17, 10 at 9:56 pm

    I think when your defi­cient in cor­ti­sol and or have something life threa­te­ning than HC is meri­ted.
    for the record I had 8 years of cor­ti­sone shots and creams for aller­gies as a kid. I have autoim­mune disea­ses and nume­rous aller­gies. They don’t run in the family. Link?Not sure I am a docu­men­ted case of an aller­gic reac­tion to Pred­ni­sone. yes there are docu­men­ted cases to such per about 10 doc­tors who wor­ked on my case and the latest autoim­mune der­ma­to­lo­gist ( really he has both degrees ) who said that the aller­gies are usually to that ” family” of ste­roid. I ima­gine its due to the carriers. I almost died after being on low dose pred­ni­sone due to my aller­gic reac­tion. The only real reac­tion I got to hydro­cor­ti­sone after 4 years was my skin tur­ned pur­plish and my throat would kinda close up for about a week after the injection.

    I’ m not being nega­tive on ste­roids for ever­yone, just for me. I have nothing but total res­pect for docs who are cau­tious with steroids.

  11. Donna said:

    Jan 18, 10 at 5:30 am

    Renee, you are extre­mely lucky! I, too, tried the “natu­ral” route for 7 long years, and saw my adre­nals become worse and worse by the year. I did the her­bals, the Adre­nal Cor­tex Extract that was tou­ted to be so natu­ral and won­der­ful, as well as acu­punc­ture, chi­ro­prac­tic treat­ments, etc. And every year, my symp­toms got worse and worse… it got to the point where I could never get out of Stage 7 adre­nal fati­gue. Yeah, I did all the things I was sup­po­sed to do to reduce my stress: divor­ced an alcoho­lic, emo­tio­nally abu­sive hus­band, moved back to my home­town to be around family, got into good the­rapy… and the the­rapy made things WORSE– because I was so cor­ti­sol defi­cient that my body couldn’t handle the stress of the­rapy twice a week. I was phy­si­cally a wreck, and had to have my mother care for my young son for seve­ral weeks. At one point, I was going to check myself into a “chro­nic fati­gue sanc­tuary” in Pennsyl­va­nia, hun­dreds of miles from my home, which cost thou­sands of dollars, and who knew how much it would improve my health? I finally came to the rea­li­za­tion that the “natu­ral” route was doing zilch for me. I found an exce­llent adre­nal sup­port group, and began HC the­rapy. A few months of tes­ting the waters with a low dose of HC led me to believe that I nee­ded a full dose of upwards of 20 mgs per day. Once I was on an ade­quate dose fo 20 mgs a day, my thy­roid labs finally sho­wed the hypothy­roi­dism that I’d suf­fe­red with for almost 10 years. In less than 2 years, I’ve gone from being bedrid­den to ope­ning up my own genea­logy research com­pany. Yes, I still need a chiro adjust­ment every month, and NOW the­rapy WORKS, because my body is no lon­ger in a fight-or-flight state. I can RELAX. I cele­brate the day I found HC, and with that, the resu­rrec­tion of my life.

  12. Andrea said:

    Jan 18, 10 at 9:34 am

    I went the direc­tion of natu­ral sup­ple­ments for trea­ting my adre­nals for about a year. I tried a variety of natu­ral sup­ple­ments, her­bal reme­dies, etc., both from the health­food store and from a natu­ro­pathic doc­tor. It was not cost effec­tive and it was not wor­king. Most made me very sick, to a point that I was una­ble to func­tion if I kept taking them. I’d end up having to stop after a cou­ple of weeks.

    After a few tries her recom­men­ded her­bals and sup­ple­ments, my ND finally presc­ri­bed HC and I woke up! What a waste of time and money, when this low dose ste­roid made me feel so much bet­ter, imme­diatly, and at a frac­tion of the cost of all those sup­ple­ments! I felt fan­tas­tic, the best I had felt in years, and had nume­rous other posi­tive “side effects” that I didn’t even expect. I would rather not have to take this stuff, but for now, it’s giving me my life back. I wish doc­tors would open their eyes and recog­nise that there are benefits.

  13. Sally said:

    Jan 19, 10 at 4:41 pm

    I star­ted on old Armour last June and bought some Iso­cort after rea­ding Stop the Thy­roid Mad­ness. I haven’t had a saliva test, but I did the pupil test and boy, did mine flut­ter like crazy! When I star­ted taking 6 Iso­cort per day, I slept bet­ter imme­dia­tely and haven’t had any acne brea­kouts. My doc­tor wasn’t fami­liar with adre­nal fati­gue and told me to take just a cou­ple of Iso­cort pellets but I had ins­tan­ta­neous bad sleep and brea­kouts so I went right back to 6.

    The doc­tor would only inc­rease my thy­roid from 60 to 70 mg (com­poun­ded) at my last appoint­ment in Octo­ber. I see him again Thurs­day and have sent him Janie’s Mis­ta­kes Patients and Their Doc­tors Make. If he won’t inc­rease it, I’ll be in the mar­ket for a new physician.

    I know I should get a saliva test, but I sure don’t want to do without the medi­ca­tion for two weeks.

  14. Dawn said:

    Jan 19, 10 at 8:46 pm

    I was diag­no­sed with adre­nal fati­gue (via very low saliva tests) and hypothy­roi­dism a few sum­mers ago. I star­ted first on HC and then added in (old) Armour. My Dr. did try to give me an adre­nal sup­ple­ment (Adren-all) while wai­ting for my saliva test results. I was nur­sing at the time and dis­co­ve­red that some of those herbs are not the best for babies, or we just don’t yet know if they’re safe. HC on the other hand, does not appear to cross into breast­milk. My many symp­toms gra­dually disap­pea­red over the next five or six months. I was on HC (20 mg) for about 8 mos. before easily wea­ning off. I trac­ked my daily tem­pe­ra­tu­res in order to deter­mine when to wean. My adre­nals then tes­ted fine. No regrets here!

    Thanks Janie for edu­ca­ting me! You have been so helpful.

  15. Enrique said:

    Jan 20, 10 at 4:25 pm

    My doc­tor AND even my mother told me I shouldn’t get on HC because it will des­troy my bones and I will gain weight.. I’m on Iso­cort for 3 months now. It seems to be wor­king but I am wea­ning myself off to do another saliva test to see where I’m at.

  16. Melissa said:

    Feb 09, 10 at 8:49 pm

    Does anyone know of a doc­tor they recom­mend in the Aus­tin, TX area?

  17. janette Ingham said:

    Apr 11, 10 at 5:48 am

    I have been on 2 x 4mg of cor­ti­sone for coming up to a year and des­si­ca­ted thy­roid. Back then my TSH was nor­mal and the doc­tors just sent me on my way but I was wan­de­ring around in a brain fog and my memory was going going gone until I had a noc­tur­nal sei­zure over a year and a half ago. I researched on the inter­net here (THANKS!) and elsewhere to try to find some help.

    Now howe­ver, my cor­ti­sol con­ti­nues to be low and after so long, my current doc­tor NOW wants me to inc­rease the cor­ti­sone another tablet and I can see why. Howe­ver, I have read up on the side effects of cor­ti­sone and I won­der if they will wor­sen if I take more. Although these can also be mixed up with my peri­me­no­pause and adre­nal pro­blems cor­ti­sone can also cause side effects such as: mis­sed periods, a sho­wing of male facial hair and lately dry, fla­king skin and the latest and worst of all my mucous mem­bra­nes seem to be shut­ting down. The inside of my nose is now cons­tantly dry and crusty, it is AWFUL! I have been taking a bunch of vita­mins as well E, C, Bs, Iron (helps the falling out hair), Zinc (for the dry skin), Fish oil, using sea salt and now Lico­rice Root in an addi­tio­nal attempt try to help the adrenals.

    Has anyone had these symp­toms on cor­ti­sone? Do you think I should still try inc­rea­sing the dose? Will these symp­toms get worse? I am still run down and still have some ongoing stress pro­blems in my life.

    Anyone else?

    Janette

    (From Janie: the side effects you are sca­ring your­self about will occur with overly high doses – those higher than your needs as one with adre­nal fati­gue. Most patients with adre­nal fati­gue report fin­ding them­sel­ves nee­ding 20 – 30 mg and some­ti­mes higher. And those who dose accor­ding to their par­ti­cu­lar need, as mea­su­red by daily ave­ra­ged temps, have no serious issues other than fee­ling much, much bet­ter and finally being able to get thy­roid hor­mo­nes to the cells, which stops dry nos­trils and fla­king skin and more. http://www.stopthethyroidmadness.com/adrenal-info and more detail in Chap­ters 5 and 6 in the STTM book. Share this infor­ma­tion with your doc.)

  18. Erika said:

    Jul 22, 10 at 7:24 am

    My doc­tor has star­ted me on 10 mg HC daily, but it’s not enough. The intense nau­sea has aba­ted and I almost sleep now, but it isn’t enough. How do I get my doc to unders­tand that more is ok, and could actually be bene­fi­cial? I have been so ill, and he keeps trying the “natu­ral route.” I have become sic­ker and crash after each new thing we try. The ONLY thing that has made me feel bet­ter is the HC. I haven’t seen my chil­dren in three months. I don’t care if more shuts my adre­nals down. If I have to be on it for life, so what. At least I will have a life.

    (from Janie: Show him Chap­ter 6 in the STTM book. Learn it and teach him. And even since the STTM book was writ­ten, we have lear­ned to “start” on 20 mg, not build up to it!! That’s on the how-to-treat page from here: http://www.stopthethyroidmadness.com/adrenal-info It does NOT shut the adre­nals down for life. )


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