Hello, I am 51 and recently diagnosed with moderate crohns in August. I was initally on predesilone tapered and subsequently Infliximab/Remicade. I am due my 4th infusion on 14th but not sure whteher to delay this as I am experiencing joint pain/weakness and hair loss. I am not sure if it is the actual crohns disease or infliximab causing this. I am in a much better place since being on it and joint pain/weakness is manageable.
I am hoping the next infusion will continue to help and reduce the flare but don't want to have it if it will make my joint pain and hair loss worse and would rather try an alternative. IBD nurses are quick to brush it off and say its the crohns although research says it could be the infliximab.
Has anyone else experienced this?