Alone with T3 and needing help, please. (New member in Ireland)

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Started on T3 (ti-tre from Teofarma, Italy) 5 weeks ago at 10 x 2 daily, now 20 x 2. Stopped T4 (eltroxin) 6 weeks ago. (split dose 125/100 5/7 days.) Consultant decided I might have conversion problem when T4 went up from 24 to 29 despite decreasing dose, severe hypo symptoms, zero hyper symptoms, and freezing, freezing cold. Within 3 days on T3 I started warming up - basal temp was 35 - now 36. Can feel my fingers again, feel brighter in my head too. (Patient information leaflet is in Italian, so have researched cytomel for guidance, and various web pages.)BUT, am having dreadful sweats, beginning late afternoon, and on through the night. Feel roasting hot but temp nowhere near normal yet. I started NAX before the T3, just 1 a day to begin with. Are the sweats related to the B vitamins, adjusting to the T3, or something else altogether? And if I take 2 NAX, what time of day should I take them? I am clearly suffering from very low adrenal researve: scored 72 total points and 176 total responses to your questionnaire, have very low BP averaging 85/55, often feel very faint and have even fainted in front of GP and consultant and during short synacthen test which was 'normal' apparently. Random noon blood cortisol was 238. Recent severe allergy to perfume/ cleaning products has put me in A and E twice now and needing adrenaline.BUT, consultant will not offer treatment "without evidence of adrenal failure".Most marvellous point about being free of T4 is that I am no longer itching all day and every day. I know this was allergy related as the only way I could cope with the itching on my face, neck and palms of my hands was with anti-histamine which quelled it temporarily. Without eltroxin this itching has gone away!I am 5ft 3, am stick thin at 7 st 4, have lost a few pounds lately, but have always been around 8 stone. Weight gain is about the only hypo symptom I don't have. My eyebrows have virtually gone from the middle and my long hair got so weak I had to get it chopped off.Some background info in case it is relevant:Now aged 58, was diagnosed in 1993, after 2 years of exhaustion and finally being deathly tired, with autoimmune hypothyoidism plus vitiligo. (first results were antibodies off the scale, TSH- 74, T4- 3. 14 months off work during which time ovaries failed and HRT started - only recently stopped this because of recurrent breast cysts.) Treated for s for 10 weeks at replacement dosage, until this was stopped by different doctor. (Have never felt as good since.) Ended up on 150 levothyoxine (in England), coped OK for 10 years until new GP began meddling and cut T4 to 100. Felt suicidal, fought to increase dose and eventually finished on 125, and went downhill from there. Move to Ireland meant change of T4 drug and eltroxin is poison to me, I am convinced of that. TSH has been undetectable for the last 5 years but I have fought to stay on 125 until very recently when I began to feel so dreadful I stopped the HRT and tried it their way, only to experience a re-run of my prediagnosis days in the early 90's.Test results:(D3, RT3 tests not possible.)Nov 2010f T3- 3.7 (2.8-6.5) (only T3 test I have ever had. Told it showed I had some T3 so I didn't need it, it would ruin my bones and heart etc etc etc)fT4 - 24.7 (10.5-22)TSH <0.02Feb 2011fT4- 26.9TSH-< 0.02July 2011fT4 29.2TSH- <0.02Feb 2011B12- 505 (187-883)folic acid- 9.2 (3-17)ferritin- 92.4 (10-200)sugar 4.6 (4.1-10)cholesterol- 6.8 (3.3-5.0) (This was steady at 4 for years but has suddenly gone up.)July 2011magnesium - 0.91 (0-38)sodium -143 (136-145)potassium - 4.0 (3.3-5.1)chloride - 105 (98-106)urea- 4.4 (2.1-7.1)creatinine - 50 (44-80)total protein- 69(64-83)albumin - 49 (39-51)total bilirubin - 10 (1-19)ALP - 67 (35-104)ALT - 16 (0-40)GGT - 39 (6-42)blood cortisol (noon) - 238 ( 7-10am 171-536nmol/L)To recap:What is causing the sweats?Can anyone suggest how long on NAX it will take for me to be able to sleep through the night, lose the feeling that my back has been broken into two pieces during the night, stop having painful cramps in my feet and calves, and generally feel less shaky and weak? My attempts to suggest these symptoms were not related to hypothyroidosm but were related to my adrenals met with absolute amazement, and a polite refusal to speak about it. Have I to wait until I collapse in an ian crisis for a doctor to listen to me? (Incidentally I am seeing one of the top endocrinology experts in Ireland and as a bonus he is a really nice man too.)Am I missing something else besides failure to convert poisonous eltroxin and adrenal problems? Please let me know.Sorry about length of this post. (I don't smoke or drink and we eat a wholesome diet, mostly home grown veg. and even have our own flock of hens and ducks for freerange organic eggs. I avoid wheat and cow's milk in all forms wherever possible.) I am a little down that I am still waiting for the cure the first GP promised me in 1993!