This last year has been awlful as well as the a... - Thyroid UK

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This last year has been awlful as well as the above have been diagnosed with menieres disease overlapping migraine symptoms are so bad

Elaine25 profile image
7 Replies

Including vertigo tinitus, nausea/vommiting, head fog eye & sound sensitive, have lost 60% of my hearing in both ears. Am off work as symtoms awlful anyone else have all the above?? Advice/ help would be great thanks

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Elaine25
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Marz profile image
Marz

Just been reading your post of a year ago. Did you manage to follow the advice ?

Could you post your blood test results with ranges for your Thyroid - AND for B12- Ferritin - Folate - VitD - Iron.

ALSO the thyroid anti-bodies - Anti-TPO - Anti-Tg.

Elaine25 profile image
Elaine25 in reply toMarz

Hi sorry not yet, last Oct they said I was on too much & reduced it bk to 100, last moth increased it bk to 125 as I really dropped & fatigue was exhausting as the menieres started in may they bn concentrating on that said mwy be a link

Marz profile image
Marz in reply toElaine25

I have read here that it is a bad plan to reduce or change medication according to the blood test results. Am I right in thinking that Menieres is an auto-immune condition ? If it is - have you been tested for auto-immune thyroiditis - Hahsimotos ? If not then the anti-bodies are called - Anti-TPO and Anti-Tg....please try to have them tested and the others suggested in the post above. We really do have to take care of ourselves and make things happen. Everyone here will help you and support.

jkiuyt profile image
jkiuyt

Have you researched the effect salt has on

Menieres? X

Elaine25 profile image
Elaine25 in reply tojkiuyt

No I will look into it thanks

jkiuyt profile image
jkiuyt

There seems to be a strong link between attacks and salt intake. Google it hun, there's lots of info out there on it. Hope it helps you. X

essdobs profile image
essdobs

My mum has late onset hypothyroidism and Meniere's also. She eats hardly any salt at all, and after 2 years of attacks certainly weekly if not daily, the meds seem to have kicked in and none for 5 months (fingers crossed!) She will be 90 next month.

The deafness has not resolved at all and I think it is permanent, she has discovered that digital hearing aids are worse than the old type, but they are very hard to come by.

She finds that by concentrating hard on her hands held close to her face can ease an attack (stopping the swirling etc) so that might help you until the meds can kick in. She is on the highest dose though.

Good luck, it is truly an horrendous thing Menieres, saps your energy and confidence too.

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