MOnica I moved from the black country Dudley heath authority. To Merseyside and the health care I have had is excellent. I only picked my GP because the bus stopped opposite. And I couldn't have chosen better.
In 2020 sent to my new neurologist who prescribed Clonazepam and after 32 years of limb jerks and 4 seizures within 2 weeks my limbs where still. He sent my blood to have my whole genome genetically tested. But didn't get sent the results until March 2022 because of covid. I was born disabled but didn't know until April 2022 what with I was finally was diagnosed with hereditary Hyperekplexia gene mutation SLC6A5 type 3.
Also my GP sent me to see a cardiologist and over 2020/2021 and was finally diagnosed with paroxysmal atrial fibrillation and found I was born with small hole in the side of my heart . And on heart medication. But I had to laugh when my cardiologist told me as I have had 3 major and 2 minor ops all with a dicky heart.
Moving here changed my life for the better healthwise and am living my life to the full instead of just existing like I did after my husband died. Moving here made my happy even though things have happened that tried to mar it. I can honestly say I have a home again and real friends and see my daughter and family regularly.
Having the 2 diagnosis my whole life finally made sense and found people with HPX. I am no longer weird but normal for HPX and PAF. Funny how life can change in a few years.
how are schools handling students who memorize books but can't actually decode
