I got her diagnosis a week ago.
My DD had fallen in height from 75 percentile to 8. She was blood tested a year ago as I was concerned about her lack of growth and was being told it was due to steroid inhalers for asthma, but they went ahead and tested her, however the hospital failed to act on the results, it just fell through the cracks. I found out December 2021 when I asked at a clinic appointment for something else. Cue quick referral to endocrinology, more blood tests and the diagnosis.
So parking the fact I am livid her treatment could have started a year ago, had anyone ent experience of this?
My son has congenital hypothyroidism so I know it quite well in terms of the development of babies and the critical developments until age 3, he was very strictly monitored and his levels controlled. Now my DD but because of hashimoto and I know next to nothing about what it means at her stage of development.
We are waiting on a bone age scan result also.
Any stories of catch up growth, successfully hitting puberty really appreciated!