Hi zebras . I have joint hypermobility and know this to be Hypermobility spectrum disorder now . I asked the doctor if I can be diagnosed with MCAS . We both agreed there is no diagnostic test so I said can he not look at what I have and do it he then said let’s get bloods done and we can go from there ? Anyone any experience of having bloods done to diagnose MCAS ( I know that there are no blood tests for this ) . Should he test for antibodies ( I already know about this as I have hashimotos disease ) . Any advice greatly appreciated

Posted by gyll5 at 2022-05-05 09:11:44 UTC