Guest guest Posted July 27, 2011 Report Share Posted July 27, 2011 Thanks for the name Bob, but I cant find it in BNF, it just tells me its not there. Will still ask anyway. Thanks again Carole > > > Hi Carole, > > It's in the BNF under ~ > > Ubidecarenone > > Bob Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2011 Report Share Posted July 27, 2011 nor me - searched bnf online, couldn't see it.... > > Thanks for the name Bob, but I cant find it in BNF, it just tells me its not there. Will still ask anyway. Thanks again > Carole Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 28, 2011 Report Share Posted July 28, 2011 " So dont be fobbed off with that old nut; we cant prescribe it. " Hi again, GP went further than that. She said she couldn't go off those blood results that I had (mitochondrial testing bloods.) Basically if it's nutritional, or un-licensed they don't prescribe it. No doubt these things vary between surgeries. In the grand scheme of things, I will have achieved something if I secure my T3 prescriptions in the long-term, which is more than I would have, where I was before. Glad you get this amount of help though, as financially it must mage a huge difference. Fiona Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 28, 2011 Report Share Posted July 28, 2011 Hi fiona, I agree. One step at a time, although it shouldnt be like that we both know. I have not been a drain on the NHS previously and it has taken me 30years of pain aggro and hassle to get a diagnosis (privately) and then treatment initiall privately. In the meantime I have tried all sorts of stuff acupuncture, herbs, reflexology, Iridology, hair analysis and multiples of supplements, nutritionalist, homeopathy oh golly you name it. I could have bought my daughter a lovely house with the money I have 'WASTED' and paid off my own mortgage, because I remained undiagnosed and untreated and with a growing list of symptoms, pains and difficulties. Then at one of my appointments for yet another infection, another GP in my surgery saw me (before diagnosis, but I had repeated said I had hypothyroidism and it was in my notes) and demanded I take Statins as my cholesterol was high and rising, (yes because I was hypoT douh! Tehe; also Statins are contraindicated in hypothyroids!!!). I do not acquiesce so easily normally, but I took them, (you get tired of fighting sometimes!) . I immediately suffered muscle pain and weakness (which remains). They were changed and this time the side effects were worse and I suffered what iI was later told was mild subarachnoid haemorrhage. It didnt feel mild I can assure you. The headaches were excrutiating and since I am used to pains in my head having suffered sevee migraines for 33years you can imagine, these were horrendous. I had not experienced these terrible headaches previously before taking Statins and the day I stopped taking Statins I stopped experiencing them. The docs all said no it wasnt the drugs, including a neurologist.!!! OK so what was it a coincidence? Hummmm I think not. When I got my diagnosis and since I had said for 30+ years I was suffering hypothyroidism and no-one listened. The damage and the trauma I suffered I think made my usual GP (who didnt prescribe the Statins) a little concerned. So when I got my diagnosis and my treatment (thanx to Myhill DOCTOR), he agreed to prescribe my treatment and the vitamins she suggested and then a few more I had previously been taking to support my adrenals (hair analysis) and one or two I added!!!! and of course the CoQ10 to TRY to improve the muscle damage I had experienced from the Statins. Bless him. I will be forever grateful. So I took what was offered. It no way compensates for all of the 30+ years lost, but its better than nothing I suppose. If I stop the CoQ10 for any reason (I get sick of taking pills and stubournly stop them occ), then the muscle pains and weakness get worse. Dr Duane Graveline has written of his experience in several books on the subject. He suffered side effects and he managed to stave the problems for a while, but I think he is now wheelchair bound! So I wont be pleased if that happens. So I dont feel at all guilty for getting this stuff, but I do tell as many people as possible so that they too may try to get the same support. I am sorry you GP is so difficult. So yes I am lucky. "So dont be fobbed off with that old nut; we cant prescribe it."Hi again, GP went further than that. She said she couldn't go off those blood results that I had (mitochondrial testing bloods.) Basically if it's nutritional, or un-licensed they don't prescribe it.No doubt these things vary between surgeries.In the grand scheme of things, I will have achieved something if I secure my T3 prescriptions in the long-term, which is more than I would have, where I was before.Glad you get this amount of help though, as financially it must mage a huge difference.Fiona Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 31, 2011 Report Share Posted July 31, 2011 hello fiona well that's shame you weren't prescribed them ...must have been wishful thinking on my part! were the specialist tests you had done (the mitochondrial function test) private tests? ...could that be why you were not prescribed coq10 ..coq10 specifically supports our mitochondria ...it would make sense to prescribe it wouldn't it! trish > > > but i was referring to getting coq10 prescribed (as opposed to getting t3 prescribed). > > > Hello Trish > > I'm afraid I don't get any coq10 or any other supplement prescribed by the GP. I recall speaking to a pharmacist, who said that none of my list of supplements are black-listed from prescription though. I guess nothing is impossible, but clearly the GPs don't see the evidence for supplements, and would rather prescribe medication only. I did ask though. > > Fiona > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 31, 2011 Report Share Posted July 31, 2011 Yes Trish, the mitochondria tests were private. You know what GPs are like, if it's not a blood test from them... Fiona. Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.