I am nearly 2 months into finding out I am primary hypothyroid (TSH was 79 with no T4) with raised TPO, but I have must have been suffering for a few years. I thought I was celiac and am now gluten free for over a year which has mostly sorted out my stomach issues.
I am nearing mid fifties and through my children's diagnosis, I realised I am dyslexic when I was about 40. I am good at maths and science just a bit slow at writing well.
Dyslexia is not all about reading and writing, as I understand it, it is about short term memory issues in listening, visual memory loops and sequencing(sentence structure etc). My short term visual is very poor and it makes copying, forms, refereeing football games harder/funnier.
I have to tell family to be please be quiet when reversing car as noise gets in way and it is quite visual.
All these memory issues have got worse with underactive thyroid, so much fatigue etc.. I would say as a child it made me less confident, as I would get things wrong. This would also change as well from day to day, which was always very frustrating. Some days flying, some days struggling.
But now it is worse. For example, in a group of people, if I am at a "bad time/foggy time", I cannot cope/filter out with two people talking at once. My dearest darling wife is very patient with me, I end up taking myself away from the group.
1) Is this the type of brain fog others experience ?
2) are there many more dyslexics in this group ? ( I did find a couple of posts in search but not much)
3) when properly medicated is the brain fog reduced ?
This Italian, paper seems to suggest a strong link autoimmune thyroid issues in children with dyslexia.
ncbi.nlm.nih.gov/pmc/articl....
Degrandi R, Prodam F, Genoni G, Bellomo G, Bona G, Giordano M, Bellone S, Monzani A. The Prevalence of Thyroid Autoimmunity in Children with Developmental Dyslexia. Biomed Res Int. 2021 Feb 8;2021:7656843. doi: 10.1155/2021/7656843. PMID: 33628813; PMCID: PMC7884110.
Abstract
Methods
We enrolled pediatric subjects with developmental dyslexia and, as a control group, healthy age- and sex-matched subjects without developmental dyslexia. Thyroid function was evaluated in subjects with developmental dyslexia measuring serum concentrations of thyroid-stimulating hormone (TSH), free triiodothyronine (fT3), and free thyroxine (fT4). Thyroid autoimmunity was evaluated in all subjects measuring antithyroid peroxidase (TPO-Ab) and antithyroglobulin (TG-Ab) antibodies. In subjects with developmental dyslexia, thyroid ultrasonography (US) was also performed.
Results
We enrolled 51 subjects with developmental dyslexia (M : F = 39 : 12, mean age 12.4 ± 9 years) and 34 controls (M : F = 24 : 10, mean age 10.8 ± 4 years). TPO-Ab positivity was significantly higher in subjects with developmental dyslexia compared to controls (60.8% vs. 2.9%, p < 0.001), while no significant difference was found in TG-Ab positivity (16% vs. 5.8%). Thyroid US performed in 49 subjects with developmental dyslexia revealed a thyroiditis pattern in 60%.
Conclusions
We found an extremely high prevalence of thyroid autoimmunity in children with developmental dyslexia. Further studies are needed to confirm our observations, but our findings may change the approach to this disorder and eventually lead to a systematic determination of thyroid autoimmunity in children with developmental dyslexia