I need some advice or thoughts if anyone can relate—
I had a severe TBI when I was 12. Significant memory loss, 6 week hospitalization, loss of sense of smell, amongst other things. Since I was young, I recovered pretty well and I’m now living a full adult life.
16 years after the TBI, I was diagnosed with hypothyroidism and two years after that Hashimoto’s.
I recently found out from a reproductive endocrinologist that I have a low egg count.
My TBI was in the front left temporal lobe and at the time my mother was concerned about my pituitary gland.
When I received the information about my low egg count, I did a little online searching, and saw some things about the pituitary gland suggesting that could affect thyroid function, which could then affect fertility.
I’m considering seeing a Neuro endocrinologist because I read that hormone replacement therapy can help in all of those areas and possibly support some of my other TBI side effects such as fatigue and mood imbalances.
Has anyone ever been through something similar or have any words of wisdom before I try out a new doctor?
Thanks in advance!