Back in January 2020 I sought my GPs advice regarding Hand tremors. I thought he might discuss Hypo symptoms or even refer me to an Endo but instead I was referred to a Neurologist. In 3 years (partly understandably through Covid) I never met the Neuro, he just phoned up and asked questions and left me on a wait list until a face to face appointment opened up. It never did and he signed me off without any diagnosis.
I have a father with Parkinson's, hence my fears.
In frustration I paid for a private Neuro consultation. After a very thorough exam, I was told it was a Levothyroxine side effect and to ask my GP for Beta Blockers. There are Heart issues in my family history so I have not done this yet. I'm reluctant to take another drug to fix an issue caused by the first.
Is this something that the lovely folk here have experience of?
Background:
Hypothyroid diagnosed in 2015 though symptomatic for several years before. On 100mg Levo and feeling OK ish. I NEVER get the same Levo brand and have been trying to determine if one or other results in fewer shakes. Sometime I find the tremor alarming, it can be an effort to use a knife and fork, my left hand is worst
I welcome your advice.