Earlier this year I had a cold that landed me in A and E when my throat swelled up alarmingly. Def wasn't a covid thing.
Since then I have had some odd symptoms I have been ignoring. Ignoring because I have a severely disabled young child who needs continual care.
I've had sore hands and feet. I'm typing this with one finger because the rest hurt too much to want to move them. Hot, swollen joints and fingers DH has likened to a pack of sausages. And my only comfortable shoes at the moment are my trainers. Fatigue that means I have been taking 2+ hour naps during the day and the simplest things tire me out to the point of exhaustion. And in the mornings DH has been calling me the tin man. Seemingly I have 'frozen' overnight and I am so stiff and sore it takes a long time (think anything up to an hour) and at least 1 cup of tea to get moving. Mornings are always worst.
It's almost like I have the flu without having the flu- especially with the body aching. I'm fairly hardened to pain anyway due to a different, physical thing but the pain in my hands is like nothing I have ever experienced before.
Still testing negative for covid- both LFT and PCR
I have an appointment Monday AM with the GP for blood tests. However I am not silly and I know where this is going. I have professional experience of RA plus my mother has it as well. Hers started in exactly the same way and it was her that pointed out my odd collection of symptoms and said I needed an appointment. And I am scared. I have seen what RA can do to people. I don't want it to happen to me. My child needs me. They'll be very unlikely to achieve independence and will always need to be cared for.
Sorry for the long message, I just wanted to get my thoughts out to a neutral place. I don't want to tell DH just yet how I am feeling.