For those who missed the This Morning Programme today - Jayne talking about her vasculitis.

[John_Mills]

This is a link to read... it’s about Jayne Hardman talking about living with vasculitis. Wegener’s Granulomatosis ( GPA ). Such an inspirational and brave lady.

digitalspy.com/tv/this-morn...

[gilders]

Thanks John. Shame it was only a 38 sec clip from the This Morning interview. I'll keep an eye out for the program she was promoting.

I'll try find the full interview. It's always good to see Vasculitis getting some exposure on national TV!

[John_Mills Volunteer in reply to gilders]

This tells you a little more about the programme Jayne took part in last night too digitalspy.com/tv/this-morn...

[lou1972]

Amazing lady. Feelings of emotion and happiness for her. We are all on here for different types of Vasculitis, but I did crumble when Jayne said you forget what you were like before the Vasculitis started.

I said those same words last weekend to my eldest daughter. I have Cutaneous Vasculitis and I don't think my legs will ever be the same again.

But Jayne was amazing and wish her well.

[Katie18]

Here’s a link to the Davina programme - I’ve just watched it on catch up - Jayne is in the last quarter of an hour so you can fast forward - amazing & very moving!

itv.com/hub/this-time-next-...

[Greenkit]

I watched this last night, Jayne is such an inspiration to everyone, she certainly lives up to the saying "never give up hope" XX

[MAC12]

What an incredibly brave woman!

[BooBoo39 Volunteer]

Thanks for that John.. What an amazing lady and such a positive role model.

[Hidden]

I often wondered why V seems to like to attack our sinus/nose. I did manage to speak to GP ..partly thanks to her raising awareness.