Mum of eight dies after spending years indoors so people wouldn’t look at her

Devoted mum and grandmother was ‘glamorous and outgoing’ until a rare illness dramatically altered her appearance

A «glamorous» mum-of-eight has died aged just 47 — after spending her last years inside her house to avoid people staring at her.

Nicola Kilby’s son Kieran has told of how she could barely bring herself to look in a mirror after a rare illness changed her appearance. She fought an inflammatory blood vessel disease for five years but the condition, Wegener’s Granulomatosis (GPA), had already started to change her appearance before she was diagnosed.

The condition attacks the ears, nose, sinuses, kidneys and lungs and, in Nicola’s case, left her deaf in both ears, damaged her soft pallet to the point that she struggled to talk, and caused her nose to collapse.

Nicola Kilby with six of her children (Image: Kieran Lane)

Nicola, a devoted mother and grandmother, died last month, after spending a number of years at home because she was so scared of strangers judging her appearance. Now Kieran, 25, hopes to raise awareness of GPA, and is fundraising towards his mum’s funeral costs and for Vasculitis UK research.

He told Birmingham Live : «My mum was an amazing person, she put everyone before herself. She was very outgoing, she was one of the most glamorous people I’ve ever met.

«She adored her children and her grandchildren and gave anyone who came through the door the warmest welcome, like they were family. She was a very strong woman and even when she was in the worst pain imaginable, she’d never let on. She didn’t want to subject anyone else to what she was going through.»

Nicola lived in Cirencester in the Cotswolds with her husband-of-ten-years, Kevin. She leaves behind eight children aged between eight and 27.

Mum-of-eight Nicola Kilby was a ‘glamorous and outgoing’ woman before Wegeners Granulomatosis took its toll on her physical and mental health (Image: Kieran Lane)

Of his mum’s battle with GPA, hotel worker Kieran said: «It’s one of the most horrendous things I can imagine anyone going through. One of the things my mum struggled with most was how dramatically her appearance changed. It ate away at her nose, she became deaf in both ears and she lost a lot of her soft pallet so she couldn’t talk properly anymore.

«Something minor like a cold would really affect her, to the point she could end up in hospital. It made the covid pandemic very difficult for her. The doctors originally said she could live for ten years with it, but it affected her very rapidly. It got to the point where she couldn’t even use the stairs, she was so weak.

«It was hard for my mum because she didn’t leave the house for years. She was so self-conscious about people staring at her.

«Even looking in a mirror was too difficult for her because of the damage it did to her nose. None of us have any pictures of my mum from the past five years because she wouldn’t allow it — not even with the grandkids on her birthday.»

Kieran recalled his mum’s reaction to an episode of ‘This Time Next Year’, with Davina McCall, where a woman from Redditch with vasculitis was given a prosthetic nose. «All my mum ever wanted was a normal nose,» he said.

«It was weird when she saw that episode on TV because most people have never heard of GPA, it’s not a word you hear often like cancer. My mum started asking questions about prosthetics. We all started looking into getting her a nose for Christmas, but all the clinics we could find were in America or they were extortionate.»

He added: «Not only did it affect her physically but it had a huge impact on her mental health as well. Because she wouldn’t leave the house, she became very isolated.

«Me and my siblings bought her a French bulldog to keep her company. It got to the point that she was so lonely that she started accepting random friend requests from strangers on Facebook so she had some friends to speak to. That’s something that really stuck with me.

«She went from being a normal outgoing mother to feeling self-conscious. She just wanted to be able to take her children to the park and do normal mum things, but it changed every part of her life completely.»

Kieran has set up a GoFundMe page to help pay towards his mum’s funeral costs. Money raised will be shared between the funeral, charity Vasculitis UK and a memorial bench to give Nicola’s children a place to visit and remember her. To donate, visit the Go Fund Me page.

Hello,

My names Kieran a son, a grandson and a brother and I’m raising money for the charity Vasculitis UK and my mothers funeral to help ease the stress on the family in a time where nothing could be more painful. Please take a moment to read and understand why, letting me break it down into two vital things.

One — My mother suffered from a long standing Illness called Wegener’s Granulomatosis or other commonly know as GPA. GPA is a type of primary systemic ANCA associated vasculitis (AAV). It is the most common type of this group of vasculitis diseases. It usually affects the kidneys, lungs, ears, nose and sinuses. GPA is characterised by inflammation of the small blood vessels including the capillaries which is a horrendous disease to endure. Even a slight cold could turn a sniffle into hospitalisation, It’s far from comfortable. She endured this for over 5 years holding on until she couldn’t no more.

Two — Funerals are unbelievably expensive and although there are many of us the cost just isn’t viable for some and this woman deserves the best send off possible. Unfortunately we can’t do it alone and that’s the hardest and saddest thing to admit. The last thing we want is for her to leave this world in the opposite way of who she was a person and in life. She was a woman of glamour and style. A beautiful wife, a loving mother and the best friend everyone deserves ! She always put others above herself no matter what. So i ask, if you can help please donate, we can’t do this alone.

So what’s the plan ?

If you donate then you help us support the chosen charity — Vasculitis UK
The majority of funds will go to the charity fighting for support against this horrendous disease, allowing sufferers to live their life more comfortably and for better research into the detection and prevention of the illness. This will all be published publicly, showing how much is given with detailed information on how you can also raise money.

The final percentage will go to her funeral. Allowing her family to say their final goodbyes and sending Nicola out in style. Easing any stress put on the family in this very tough time, she was a pillar to so many in life and without her they are beyond lost.

We hate to ask but if you can donate even the tiniest amount then Our mums life meant something and with the money raised can change/help someone else going through the same as she did knowing that they won’t suffer the way she did. Please donate what you can ❤️ R.I.P mum this one’s for you xx

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