Nearly 14 years post transplant here and not really worrying.
Putting all the effort into taking whatever steps I need to, in order to minimise risk as much as possible.
Have had a letter from my unit this week outlying what to do if I think I have it - same as everyone else really - call 111 but tell them you're a transplant recipient.
Keep taking the tablets etc.
Letter gives contact number for transplant Nurses, which I have anyway.
I have such faith in my transplant Consultant and her team, so I know they are just a phone call away if I need advice.
My next outpatient appointment has been changed from face to face to phone consultation and, quite frankly, I'm delighted!
I've been requesting this for a long time but Doc was reluctant as she likes to see her patients in the flesh.
I have a couple of questions regarding blood tests and supply of anti rejection meds but will phone Nurses next week as I'm sure they will have been innundated once those letters went out.
I'm not going out from hereonin and am cleaning things I never dreamt of cleaning in the past eg. light switches, plugs, sockets, glasses - including the arms, TV remote, phones, tablets and their cases, in short, everything that is touched! - I've even washed my door keys!!
The Goverment Coronovirus advice info which was published earlier this week, did say that we transplanted would be written to by "The NHS" with further specific advice for "us".