mandy

Before it all kicked off with me, I'd already Noticed I was becoming intolerant to things I couldn't drink pepsi max anymore would Be bloated etc but also jittery and anxious (Maybe the caffine) I used to consume: Muller light yogurts Cadburys hi lights hot chocolate (used to mix it With my porrige and have it for breakfast Was sooooo nice) Both of these have aspartemaine in them. When I started out my journey I ended up at A homeopath she said out of everything Your not good with aspartemane is the worst For me!! I really notice now if I do have something with a

Hi.. I've got acv ..when I take it ..it makes my reflux even worse -ve not taken it oftern enough to see any real Results to get rid of fungi. Peaches - so is this why I feel better on Totally yeast free diet? The trouble is its so restrictive and even With a homeopath and taking special supplemsnts For 8 months it won't go... Do you think I could screw test results by doing such A strict candidas diet? I just eat egg, lean meat and fish, veggies ( No corn, carrott or potatoes), olive oil, Some salad, tiny amount of skim milk... Is the fungi mainly a cushy probl

This is so true, we are living proof of this!!! Glad its getting noticed!! I went to see my GP as specialist put me on tablets and was 10mg I was having major head pressure, facial pain, even more anger, suicidal,crying anxious, Foot cramps all this stuff but couldn't get hold of my specialist.. So I went to GP as you'd think you'd get some support! He said there's no point Coming here I don't know what's wrong with you! Your under specialist And you've had a lot of tests they may find what's wrong with you in 100 years But its likley you'll never get better and will have to live

Yes, flouride is a problemb for hypothyroid..which is why tea is bad for hypot's apparently

I'm not suprised!! All the crap put in our food, antibiotics given out so frequently!! Seems as though all these rare diseases aren't that rare anymore...probably where they are Poisoning us...with medsand food!! Now toothpaste!!

Hope it may help some one on here!! http://www.endocrinology.org/meetings/2007...urseBooklet.pdf XX

Hi Guys, I found this whilst trying to find confirmation that you can have low DHEAS in cushings and it discusses a patient who has same as me high androstenedione and low normal DHEA. Ive got the endo calling me soon and will be going back to see them at Barts, so Iam feeling stronger again and more confident that it is more than just a thyroid problem (With the help of a special lady on here and a lady on a thyroid forum). RESULTS Plasma cortisol values of 15 patients with Cushing's disease (range 326?1140 nmol/l, normal range 190?690 nmol/l) were elevated in 9; In contrast, plas