Hello again. Just had repeat blood tests to check I'm on the right dose of Carbimazole. I have been diagnosed with graves disease and have decided to take the tablet route first. I've noticed a massive amount of hair loss in recent weeks and was hoping it was just my tablets that needed altering but endo had said I'm normal now. TSH 2.58
T4 13.3
T3 4.5
Any suggestions as to why I'm losing hair if my levels are OK??? Any suggestions to stopping it?
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Spagbol24
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That’s frustrating, you can request copy of test results via endocrinology department secretary / receptionist- or most hospital have records department with a set form to request records. Can be done by email / may need ID & witness signature.
Doctors view 5mg as lowest possible dose, but you can split a pill of take every other day. So if you do learn the FT4 & FT3 are low speak to you doctor about lowering dose.
Low ferritin can often affect hair, has that been tested?
I was told by my endocrinologist that the hair loss was from the initial onslaught of the thyroid going wrong. I had hair loss for quite a while and even when my levels got back in range. The condition of my hair also changed too. It became quite brittle and lacking substance. It stopped over time and recovered so don’t be too worried about it.
Thank you. I was wondering about that. Whether it could be delayed from before when I wasn't on medication. I had a thyroid storm in January... so maybe its the after effects of that. I do appreciate your reassurance
I think your T3 and T4 now ' look too low ; wht are the ranges and this may well cause disabling symptoms.
Hair loss could also be down to iron levels ?
When metabolism runs too fast as in hyper or too slow as in hypo the body struggles to extract key nutrients through food no matter how well and clean you eat -
so it's sensible to also get your core strength vitamins and minerals run as non optimal levels of your ferritin, folate, B12 and vitamin D can compromise your ill health further than necessary.
You do not need to accept RAI thyroid ablation - many people say No - and stay on the AT drug and if this doesn't work out well for them - opt for a thyroidectomy - so please try and find a way forward on the least invasive option - the Anti Thyroid drug.
I sent you the links to the research papers suggesting RAI is not the best option for the patient - just print these out and if feeling pressured discuss these findings with your endocrinologist and doctor.
To be honest, the hair loss has taken a back seat cause I had a small spot removed from my tongue two weeks ago and I now think that's triggered Burning Mouth Syndrome. It never seems to end at the moment
Can you please supply your blood test results at diagnosis and which antibodies were found over range and positive and the medical evidence attached to having Graves Disease.
I ask as there are 2 AI diseases that effect the thyroid and often confused in the first phase of an overactive thyroid but only Graves is treated with an Anti Thyroid drug.
Your TSH has recovered well and no longer under an immune system attack - which is a little unusual this quickly when with Graves Disease.
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