Kat's Skyrizi Journey Part 2

[Caroline]

As you know I’m also on Skyrizi.
Years ago I had scalp p for a while. I’ve not had any since.. until now, on Skyrizi.
I’ve also developed inverse p - which I’ve never had before.
I am seeing the derm soon, I know she wants me to stay on it.
I’m getting a bit fed up with their one drug fits all attitude, if it’s not working why are we being made to feel like we’re not ‘trying’ hard enough?

It is recognisable over here.
Recently there was a congress, the EADV congress, of dermatologists and other. Over there they were talking about all the choices that were there, advanced treatments and the state of medics.
I heard there was also a patient, telling the real situation and who said that all those great presentations on new drugs and patient centric treatments, but the real world was still the old fashioned way of trying everything so you could finally find the right treatment for yourself…..after…. 10 years or so.