Since starting on thyroxine back in May this year, I've had increasing problems with an indigestion feeling in my throat. I've read about l-glutamine and gut healing, so definitely think I need something to help this but don't want to risk any tumours that I don't know about growing in size. My Dad died of stomach cancer.
Does anyone else have this indigestion feeling in their throat? It's not severe but reminds me that I'm probably not doing enough to heal my gut. I take digestive enzymes and probiotics when I remember but it's now more difficult to fit more supplements in as I take two doses of T3. The symptom seems to be worse again after starting T3.
I've taken apple cider vinegar with mother twice a day for months and find this easier to fit into my schedule. Hopefully it's helped digestion in general but hasn't helped this symptom. Has anyone had reduction in these symptoms with another supplement?
Thanks in advance for any advice and sharing of experiences.
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Highland49
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Thanks shaws, I need to try and take them more regularly. Some days I felt the betaine/pepsin ones were making me worse but difficult to say for definite.
Keep some in your handbag so you have them to hand if you are eating out. You can also put them on your table so that it is easier to remember. Also as SlowDragon suggests, it could be the Teva (if you take that make).
If not, it's time to ask GP to get your stomach checked.
I definitely want to try Mercury Pharma next time round. It's working out for taking my second T3 as I have that in my pill box when I'm out and about but I now need another phone reminder for the probiotics!
Thanks for your reply SlowDragon. I've only taken Teva as I was prescribed 75mcg and this dose hasn't changed (except my reduction when I started T3).
I don't believe I'm lactose intolerant but any dairy eaten fairly recently made my breathing worse so have gone dairy free for the last 3 months at least. I'm hoping when I return to endo in December that he reduces my levo dose then I can take a different brand and see if that is any better. Maybe Mercury Pharma will be better. I am right in thinking that 75mcg is only manufactured by Teva?
Thanks for your reply and all that information SlowDragon. Saying about needing a dose increase, I've increased my levo back to the 75mcg from the 50 as felt more lethargic.
I'm definitely improving but I do wonder if I would do better on a different brand.
To help with my next battle of T3 on the NHS, my results are available on the DIO2 gene test so I just need to see if my endo will have the results sent to him or whether I'll need to pay for the independent practitioner through Regenerus. It's good that they have their code of conduct but I just want the answer, yes or no!
Unfortunately I've already emailed the secretary but of course, they might not be happy to be involved. What's your reason for advising against it SlowDragon?
I'm very lucky that he's already prescribed T3 so let's hope it doesn't affect his future prescribing if I don't test positive. So not straightforward all this, eh?
Getting DIO2 gene test, definitely helped strengthen my argument to be prescribed on NHS. I think it also got me a slightly higher dose than might have been prescribed otherwise
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