Hope everyone is well and enjoying a bit more freedom now lockdown is starting to ease down. I must say I'm looking forward to getting back to some kind of normality, especially ' visiting 'restaurants and pubs'
Feeling guilty posting about pain with RA when so many people have lost their life through Covid19, but need some advice. My RA has been treating me well over the last 6 months ( I'm on Adalimumab) however I've noticed that my joints have started to get angry! A few days prior to injecting my joints: balls of my feet, hands and knees start to to get very painful., not sure this is normal, today I found it hard to take my injection. It s very worrying that success is short lived! I'm worried that my RA is more severe than I thought or after 18 months i still havent found the right meds. Maybe Biosimilars are just not as effective? I have spoken to my nurse, she wants me to stay on them for another 3 months yuk! I have a very busy time coming up so very bad timing!