Thenursemum

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Did UGG start a fundraiser too separately to the one Rosie/Susie and Megan Rose Lane did alongside Kaytees own? Was there 3 or 4 fundraisers then? I only knew of the 3 😯 how much was raised on that one, do you know?

I thought she did it with Susie? Or was part of it defo not one on her own I don’t think. I mean the fact there’s been 3 is insane when so many other families get nothing.

Can I ask who UGG is please?

She’s v funny and easy going. One of the only influencers I like really because she ain’t in it for money or fame. And she doesn’t pimp her kids out
 
Phew! I thought there was a 4th on the go then. Susie Verrill and Rosie Ramsey set one up together but lots of other influencers shared theirs. Most families who really do need help dont even set one up now after what Kaytee did. She has made people look at them differently, with caution and suspicion. Theres alot of worry amongst SEND parents that people will think their fundraisers wont be legit because of what shes done. She has caused alot of harm to the children who do need that financial support, many need people to help straight away but now alot of fundraisers take months to reach their targets and alot of those children dont have months to wait. You only have to read on here and see that people have commented that they no longer donate to fundraisers because of her. I hope she is proud of herself knowing other children are suffering the consequences of her actions.

If people read this and feel that way, please reconsider and be assured that other SEND parents struggle to ask for help, it's a last resort for many, if you see one of their fundraisers please support it, it wont be used to buy a hot tub or fancy hotel stays. Come and find us on Instagram, search other SEND accounts and you will see for yourselves the reality of our lives are very different to Kaytees and she is not our voice.
 
Phew! I thought there was a 4th on the go then. Susie Verrill and Rosie Ramsey set one up together but lots of other influencers shared theirs. Most families who really do need help dont even set one up now after what Kaytee did. She has made people look at them differently, with caution and suspicion. Theres alot of worry amongst SEND parents that people will think their fundraisers wont be legit because of what shes done. She has caused alot of harm to the children who do need that financial support, many need people to help straight away but now alot of fundraisers take months to reach their targets and alot of those children dont have months to wait. You only have to read on here and see that people have commented that they no longer donate to fundraisers because of her. I hope she is proud of herself knowing other children are suffering the consequences of her actions.

If people read this and feel that way, please reconsider and be assured that other SEND parents struggle to ask for help, it's a last resort for many, if you see one of their fundraisers please support it, it wont be used to buy a hot tub or fancy hotel stays. Come and find us on Instagram, search other SEND accounts and you will see for yourselves the reality of our lives are very different to Kaytees and she is not our voice.
I would love to follow you on Instagram 💖
 
If any of you follow the proper SEN parents who support each other, by not only putting in others fundraisers but sharing other children's milestones, celebrating their success and achievements.... And also rallying around to support parents when they are struggling with their mental health... And being an army of support when one of the SEN community looses a child.... You will see that Kaytee is definitely not in this category.

The parents who continously push their child, who do all therapies themselves, researching for anything to help their child, fighting to show others that disabilities are not something to fear.. To pity. But something to love... To include just like any other minority in society. They are always educating in a polite and nice way. They play with their children. They create bucket lists that instead of a trip to dubai... Its "jump in a muddy puddle" whilst holding their quadriplegic child who cannot hold their own head up let alone jump unaided.

The parents who have to swallow their pride to fundraise for treatment in another country... For a walker because the NHS won't fund... Who show you that after purchasing, who don't have influencer friends that can share their fundraiser. Who do raffles, tombolas, challenges, auction nights to raise that money that will literally be life saving or enhancing their child's life.

The parents who have much more complex children. Who cannot do half of the amazing abilities kaytees son can do. Who never ever focus on what they can't do.... But what they can. The slight movement in their hand, they've coughed to clear their throat for the first time... They've managed to press a switch to consistently say yes to a closed question to communicate because they cannot communicate AT ALL.

Those parents never play on their child's disabilities. They never play the pity card. Who never seem to moan... They just get on with it. Those parents who all followed kaytee and watched her charade from THE VERY BEGINNING. This hasn't just been after the fundraisers. This has been since the day she started her account. Many of us do not stop and think to take a photo of our child getting into an ambulance. We do not think to film our children vomiting, screaming, looking desperately thin, leaving our children in hospital to go get pissed on a golf course.

The parents who sleep upright in a chair beside their child. Who have had a much tougher ride than kaytee. Watching her tell her followers how severe her sons abilities are. Insisting her son scores high in areas their children do when her son doesn't even qualify to score low on these areas. Who constantly uses her son to gain popularity.

That woman will never in a million years represent the SEN community I follow and am part of. Her whole outlook on disabilities, her using that as her platform to get ad work... To fund a lifestyle she has always wanted from the start of her Instagram blogging. The only reason people are seeing it more is because it's getting more frequent, her lies and inconsistencies are beginning to catch up with her. But I assure you they have always been there.
That woman has never wanted to be an advocate for this community. She's wanted carers for herself because she cannot cope. She doesn't want to care for her child. She wants others to do that whilst she lives her influencer, adventure lifestyle.

Her blatent lack of compassion to others in a worse position than herself disgusts me. For someone wanting to be the voice of a community she supposedly cares for, she has treated them appaulingly.
 
If any of you follow the proper SEN parents who support each other, by not only putting in others fundraisers but sharing other children's milestones, celebrating their success and achievements.... And also rallying around to support parents when they are struggling with their mental health... And being an army of support when one of the SEN community looses a child.... You will see that Kaytee is definitely not in this category.

The parents who continously push their child, who do all therapies themselves, researching for anything to help their child, fighting to show others that disabilities are not something to fear.. To pity. But something to love... To include just like any other minority in society. They are always educating in a polite and nice way. They play with their children. They create bucket lists that instead of a trip to dubai... Its "jump in a muddy puddle" whilst holding their quadriplegic child who cannot hold their own head up let alone jump unaided.

The parents who have to swallow their pride to fundraise for treatment in another country... For a walker because the NHS won't fund... Who show you that after purchasing, who don't have influencer friends that can share their fundraiser. Who do raffles, tombolas, challenges, auction nights to raise that money that will literally be life saving or enhancing their child's life.

The parents who have much more complex children. Who cannot do half of the amazing abilities kaytees son can do. Who never ever focus on what they can't do.... But what they can. The slight movement in their hand, they've coughed to clear their throat for the first time... They've managed to press a switch to consistently say yes to a closed question to communicate because they cannot communicate AT ALL.

Those parents never play on their child's disabilities. They never play the pity card. Who never seem to moan... They just get on with it. Those parents who all followed kaytee and watched her charade from THE VERY BEGINNING. This hasn't just been after the fundraisers. This has been since the day she started her account. Many of us do not stop and think to take a photo of our child getting into an ambulance. We do not think to film our children vomiting, screaming, looking desperately thin, leaving our children in hospital to go get pissed on a golf course.

The parents who sleep upright in a chair beside their child. Who have had a much tougher ride than kaytee. Watching her tell her followers how severe her sons abilities are. Insisting her son scores high in areas their children do when her son doesn't even qualify to score low on these areas. Who constantly uses her son to gain popularity.

That woman will never in a million years represent the SEN community I follow and am part of. Her whole outlook on disabilities, her using that as her platform to get ad work... To fund a lifestyle she has always wanted from the start of her Instagram blogging. The only reason people are seeing it more is because it's getting more frequent, her lies and inconsistencies are beginning to catch up with her. But I assure you they have always been there.
That woman has never wanted to be an advocate for this community. She's wanted carers for herself because she cannot cope. She doesn't want to care for her child. She wants others to do that whilst she lives her influencer, adventure lifestyle.

Her blatent lack of compassion to others in a worse position than herself disgusts me. For someone wanting to be the voice of a community she supposedly cares for, she has treated them appaulingly.
Bravo my lovely, Bravo! 😘😘😘

I was only thinking today she has no shame, embarrassment or guilt about what she has done and continues to do. And you are so right in pointing out this isn’t new. I see a lot of people who think she’s changed or has recently shown her true colours yet we have seen it for much longer. Like you say since the beginning. It’s just more obvious now because she feels invincible and untouchable....so why even pretend.
 
Phew! I thought there was a 4th on the go then. Susie Verrill and Rosie Ramsey set one up together but lots of other influencers shared theirs. Most families who really do need help dont even set one up now after what Kaytee did. She has made people look at them differently, with caution and suspicion. Theres alot of worry amongst SEND parents that people will think their fundraisers wont be legit because of what shes done. She has caused alot of harm to the children who do need that financial support, many need people to help straight away but now alot of fundraisers take months to reach their targets and alot of those children dont have months to wait. You only have to read on here and see that people have commented that they no longer donate to fundraisers because of her. I hope she is proud of herself knowing other children are suffering the consequences of her actions.

If people read this and feel that way, please reconsider and be assured that other SEND parents struggle to ask for help, it's a last resort for many, if you see one of their fundraisers please support it, it wont be used to buy a hot tub or fancy hotel stays. Come and find us on Instagram, search other SEND accounts and you will see for yourselves the reality of our lives are very different to Kaytees and she is not our voice.

I’d follow and support. I’m not a SEND mother but my
Godson has Duchenne Muscular Dystrophy and I can imagine the fear, and the need for help with equipement etc.

I wish I could do more to shout about those in need and why. I don’t feel I know enough about these things to be able to give SEND needs justice and that’s my own fault. I will Endeavour to learn and read more.

I’m ashamed to say I was a follower of Kaytee and felt sorry for her. I feel like I’ve been scammed. A bit like PTWM who did a number on people for charity money and kept it for herself.

WHY DO PEOPLE DO THIS???

If any of you follow the proper SEN parents who support each other, by not only putting in others fundraisers but sharing other children's milestones, celebrating their success and achievements.... And also rallying around to support parents when they are struggling with their mental health... And being an army of support when one of the SEN community looses a child.... You will see that Kaytee is definitely not in this category.

The parents who continously push their child, who do all therapies themselves, researching for anything to help their child, fighting to show others that disabilities are not something to fear.. To pity. But something to love... To include just like any other minority in society. They are always educating in a polite and nice way. They play with their children. They create bucket lists that instead of a trip to dubai... Its "jump in a muddy puddle" whilst holding their quadriplegic child who cannot hold their own head up let alone jump unaided.

The parents who have to swallow their pride to fundraise for treatment in another country... For a walker because the NHS won't fund... Who show you that after purchasing, who don't have influencer friends that can share their fundraiser. Who do raffles, tombolas, challenges, auction nights to raise that money that will literally be life saving or enhancing their child's life.

The parents who have much more complex children. Who cannot do half of the amazing abilities kaytees son can do. Who never ever focus on what they can't do.... But what they can. The slight movement in their hand, they've coughed to clear their throat for the first time... They've managed to press a switch to consistently say yes to a closed question to communicate because they cannot communicate AT ALL.

Those parents never play on their child's disabilities. They never play the pity card. Who never seem to moan... They just get on with it. Those parents who all followed kaytee and watched her charade from THE VERY BEGINNING. This hasn't just been after the fundraisers. This has been since the day she started her account. Many of us do not stop and think to take a photo of our child getting into an ambulance. We do not think to film our children vomiting, screaming, looking desperately thin, leaving our children in hospital to go get pissed on a golf course.

The parents who sleep upright in a chair beside their child. Who have had a much tougher ride than kaytee. Watching her tell her followers how severe her sons abilities are. Insisting her son scores high in areas their children do when her son doesn't even qualify to score low on these areas. Who constantly uses her son to gain popularity.

That woman will never in a million years represent the SEN community I follow and am part of. Her whole outlook on disabilities, her using that as her platform to get ad work... To fund a lifestyle she has always wanted from the start of her Instagram blogging. The only reason people are seeing it more is because it's getting more frequent, her lies and inconsistencies are beginning to catch up with her. But I assure you they have always been there.
That woman has never wanted to be an advocate for this community. She's wanted carers for herself because she cannot cope. She doesn't want to care for her child. She wants others to do that whilst she lives her influencer, adventure lifestyle.

Her blatent lack of compassion to others in a worse position than herself disgusts me. For someone wanting to be the voice of a community she supposedly cares for, she has treated them appaulingly.

I want to say I feel completely stupid (can’t think of a better word) for being fooled by this person and for even slightly thinking she’s so
Much worse off compared to others.
 
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Bravo my lovely, Bravo! 😘😘😘

I was only thinking today she has no shame, embarrassment or guilt about what she has done and continues to do. And you are so right in pointing out this isn’t new. I see a lot of people who think she’s changed or has recently shown her true colours yet we have seen it for much longer. Like you say since the beginning. It’s just more obvious now because she feels invincible and untouchable....so why even pretend.
This is what I don't understand when I see people say... Since the fundraisers. No. This behaviour hasn't started since then... This behaviour of hers has been there right from the start. She's known all along the direction she wants to go, knowing how to go about that thru filming herself in hospital, portraying herself as single mum kaytee to a very complex child living in hospital, she's not the first.... There are thousands who have been in her shoes and have lived in hospitals a lot longer. Not that it's a contest as to whose had a tougher ride but the way she writes, and portrays herself you'd think she's the only woman in the world to have stayed in a hospital with her poorly child. She knows graphic pictures and videos will get people giving her attention. It's quite concerning that the first thing that enters her head when an ambulance comes is to get out her phone to take a picture or video to post on social media. Her whole life is for social media. Non of it is private, except her family and her sons dad that she purposefully doesn't talk about and plays down because she knows that doesn't fit with her narrative.
She's a narcissist. Plain and simple. And that has had to have been there way before her son came along. She used to have a fb account that you could see past status's on there... An old twitter account all of which have been either deleted or privacy settings changed because she doesn't want people seeing.
She used to run a pole dancing class at university. From the stuff I've seen and read there must have been some bad blood there too. She isn't the nice person people think. I don't understand when people say she's a brilliant mother because she isn't.

Her son is amazing. His abilities should be shouted from the roof tops. Because he's doing fantastically well.
But kaytee I am sorry is a nasty, attention seeking manipulator and she's pulling the Puppet strings on every one of her followers.
 
If any of you follow the proper SEN parents who support each other, by not only putting in others fundraisers but sharing other children's milestones, celebrating their success and achievements.... And also rallying around to support parents when they are struggling with their mental health... And being an army of support when one of the SEN community looses a child.... You will see that Kaytee is definitely not in this category.

The parents who continously push their child, who do all therapies themselves, researching for anything to help their child, fighting to show others that disabilities are not something to fear.. To pity. But something to love... To include just like any other minority in society. They are always educating in a polite and nice way. They play with their children. They create bucket lists that instead of a trip to dubai... Its "jump in a muddy puddle" whilst holding their quadriplegic child who cannot hold their own head up let alone jump unaided.

The parents who have to swallow their pride to fundraise for treatment in another country... For a walker because the NHS won't fund... Who show you that after purchasing, who don't have influencer friends that can share their fundraiser. Who do raffles, tombolas, challenges, auction nights to raise that money that will literally be life saving or enhancing their child's life.

The parents who have much more complex children. Who cannot do half of the amazing abilities kaytees son can do. Who never ever focus on what they can't do.... But what they can. The slight movement in their hand, they've coughed to clear their throat for the first time... They've managed to press a switch to consistently say yes to a closed question to communicate because they cannot communicate AT ALL.

Those parents never play on their child's disabilities. They never play the pity card. Who never seem to moan... They just get on with it. Those parents who all followed kaytee and watched her charade from THE VERY BEGINNING. This hasn't just been after the fundraisers. This has been since the day she started her account. Many of us do not stop and think to take a photo of our child getting into an ambulance. We do not think to film our children vomiting, screaming, looking desperately thin, leaving our children in hospital to go get pissed on a golf course.

The parents who sleep upright in a chair beside their child. Who have had a much tougher ride than kaytee. Watching her tell her followers how severe her sons abilities are. Insisting her son scores high in areas their children do when her son doesn't even qualify to score low on these areas. Who constantly uses her son to gain popularity.

That woman will never in a million years represent the SEN community I follow and am part of. Her whole outlook on disabilities, her using that as her platform to get ad work... To fund a lifestyle she has always wanted from the start of her Instagram blogging. The only reason people are seeing it more is because it's getting more frequent, her lies and inconsistencies are beginning to catch up with her. But I assure you they have always been there.
That woman has never wanted to be an advocate for this community. She's wanted carers for herself because she cannot cope. She doesn't want to care for her child. She wants others to do that whilst she lives her influencer, adventure lifestyle.

Her blatent lack of compassion to others in a worse position than herself disgusts me. For someone wanting to be the voice of a community she supposedly cares for, she has treated them appaulingly.

I think I love you for this!
 
I dont like how she builds things up so followers begin to fret or wonder what's going on. She filmed him being wheeled down for his MRI under GA 22 hours ago, she's been mentioning the dangers around GAs for J quite a bit recently, she saw fit to share him being wheeled down yet theres been no update since. GOSH work off 2 lists a day for MRI under GAs.

It doesnt matter if your on the morning or afternoon list, your child is usually discharged within a few hours of the MRI even if your on the afternoon list, they very rarely stay in unless theres complications or severe side effects of the GA. J was having a MRI not a procedure or surgery. GOSH are used to doing MRIs under GAs for medically complex children who are high risk under GA, she has mentioned having to have a specialist present during the MRI but that is nothing new and pretty standard from our own experience plus other GOSH children I know. GOSH are the best of the best, they will have specialists present just to be on the safe side.

Kaytee knows her followers are invested in J, her DMs will be full of people concerned as she hasnt given a update that things went ok. If she saw fit to film him before, but hasnt seen fit to update everyone after, it makes you wonder if something has happened or if she purposely delays in updating people for the attention. She has done this before, built it up so people are waiting for news that alls ok but then leaves it ages before updating. It does make you worry about J, it makes you check her account for news and so many will be thinking of him not knowing if hes ok.
 
I dont like how she builds things up so followers begin to fret or wonder what's going on. She filmed him being wheeled down for his MRI under GA 22 hours ago, she's been mentioning the dangers around GAs for J quite a bit recently, she saw fit to share him being wheeled down yet theres been no update since. GOSH work off 2 lists a day for MRI under GAs.

It doesnt matter if your on the morning or afternoon list, your child is usually discharged within a few hours of the MRI even if your on the afternoon list, they very rarely stay in unless theres complications or severe side effects of the GA. J was having a MRI not a procedure or surgery. GOSH are used to doing MRIs under GAs for medically complex children who are high risk under GA, she has mentioned having to have a specialist present during the MRI but that is nothing new and pretty standard from our own experience plus other GOSH children I know. GOSH are the best of the best, they will have specialists present just to be on the safe side.

Kaytee knows her followers are invested in J, her DMs will be full of people concerned as she hasnt given a update that things went ok. If she saw fit to film him before, but hasnt seen fit to update everyone after, it makes you wonder if something has happened or if she purposely delays in updating people for the attention. She has done this before, built it up so people are waiting for news that alls ok but then leaves it ages before updating. It does make you worry about J, it makes you check her account for news and so many will be thinking of him not knowing if hes ok.

THIS. So now I’ve seen her for what she’s really like it winds me up that’s she’s left people dangling when she wouldn’t ever do that normally on a daily basis. Even if something was wrong she’d be on SM because she can’t help herself it seems
 
I dont like how she builds things up so followers begin to fret or wonder what's going on. She filmed him being wheeled down for his MRI under GA 22 hours ago, she's been mentioning the dangers around GAs for J quite a bit recently, she saw fit to share him being wheeled down yet theres been no update since. GOSH work off 2 lists a day for MRI under GAs.

It doesnt matter if your on the morning or afternoon list, your child is usually discharged within a few hours of the MRI even if your on the afternoon list, they very rarely stay in unless theres complications or severe side effects of the GA. J was having a MRI not a procedure or surgery. GOSH are used to doing MRIs under GAs for medically complex children who are high risk under GA, she has mentioned having to have a specialist present during the MRI but that is nothing new and pretty standard from our own experience plus other GOSH children I know. GOSH are the best of the best, they will have specialists present just to be on the safe side.

Kaytee knows her followers are invested in J, her DMs will be full of people concerned as she hasnt given a update that things went ok. If she saw fit to film him before, but hasnt seen fit to update everyone after, it makes you wonder if something has happened or if she purposely delays in updating people for the attention. She has done this before, built it up so people are waiting for news that alls ok but then leaves it ages before updating. It does make you worry about J, it makes you check her account for news and so many will be thinking of him not knowing if hes ok.

We all know his dad lives in London. It’s highly likely she has taken him there and could either be in a hotel again or back home in Nottingham for a child free weekend.
Not the first or last time it’s alluded to that something is wrong when it’s simply her being shady. No she doesn’t have to check in with SM and her life is her own but the image she portrays, the sympathy she expects and now the financial investments she demands from her followers means she has a duty to say if all is well or not.
And I don’t know anyone else who has used a stories to show themselves after finding out a friend has passed away.
 
Sorry it’s munchausin by proxy.

In the UK it's now known as FII, fabricated induced illness. It's a tricky one, it's extremely rare although it might not be as rare as people think as many case go undetected/reported. If you take 100k children there wont even be 100 cases of FII as it is that rare. It's a really rare form of child abuse but a really serious form.

It's not a nice thing for any of us in the SEN community to accuse other parents of. A high proportion of parents are treated as though they are fabricating their childrens symptoms, for instance ASD parents trying to get a ASD diagnosis for their children are often parent blamed, told they are exagerratting their childs needs and abilities, behaviours are blamed on parenting or trying to get disability benefits. Its very rarely the case but its the go to thing for professionals who dont take into account how rare and unlikely it is to be the case.

FII is complex, it can be done for different reasons, most cases are done by the mother and usually because they enjoy being the caregiver and the attention/sympathy they get from others. There has also been cases of FII for financial gain, those who have fabricated or caused their child to become ill or to increase their childs needs and decrease their abilities, in order to claim disability benefits or raise money. This is really rare.

Most people think FII is done by a parent with children who are 100% fit and healthy, infact it can be either those with existing diagnoses or those with no health concerns at all.

Regardless of if Fii is the case here or not, this is the damage Kaytee is doing to the SEN community. People will be talking, looking at her actions and as she claims to be the voice of the sen community, people will start to wonder about others. Theres alot of SEN parents who give up fighting for assessments and diagnoses because of professionals judging them instead of listening and assessing the child first. If Kaytee is ever found to be FII the damage to the sen community could be horrific.

Whether FII is the case or not, without a doubt the professionals around them will be looking at FII being possible. She has created alot of attention around her so they will be viewing her page just like we do. They will 100% know more information than any of us do.

They will notice things we wont even notice. For instance if Kaytee has exaggerated or lied about meetings, assessments and decisions that have been made. They will know what attitude she has with professionals, how she acts in meetings, they may have reports off people who have reported her or raised concerns. There may be meetings and appointments that she has failed to attend. They will be concerned if communication with them is poor but she is constantly online. They will know about the fundraisers and will have noted the things she claimed she needed money for was funded and she never admitted that until weeks later once alot of money had been raised. There may be concerns raised by carers, we already know she was reported by one for coming home drunk and having a domestic. They will be concerned with why she doesnt disconnect his tube leading it to cause discomfort and increasing the risk of infection which increases the likelihood of hospital visits and admissions. She may have already been told about this which will concern them more if they are viewing her page and seeing she is still doing it. They will know shes aware missing meds and feeds can cause devastating consequences but she admits to doing it. The feeding school programme would have been another red flag because they will know GOSH advise ALL parents against this.

Each thing is a individual safeguarding concern, so collectively she is causing a huge safeguarding issue. As she has put her self into the public arena, there is no way they will overlook things in her case, and it wouldn't be the first or last time professionals got their own back for being made to look bad publically.

Without a doubt FII will be a concern for them that they have already noted and may be looking into. They have professionals dutys and I would not be shocked if they have raised quite a few safeguarding concerns. It's not for any of us to say if FII is the case here and people should be mindful that it is incredibly rare. But her own actions are questionable and professionals have a legal duty to act on concerns. If a professional even read this thread they would be duty bound to report safeguarding concerns. J should be on a CIN plan, if that has not been progressed to a child protection plan I would put money on it being progressed to that level soon.

We all know his dad lives in London. It’s highly likely she has taken him there and could either be in a hotel again or back home in Nottingham for a child free weekend.
Not the first or last time it’s alluded to that something is wrong when it’s simply her being shady. No she doesn’t have to check in with SM and her life is her own but the image she portrays, the sympathy she expects and now the financial investments she demands from her followers means she has a duty to say if all is well or not.
And I don’t know anyone else who has used a stories to show themselves after finding out a friend has passed away.

Shes also removed the grid picture of her and her friend which seems odd to me and a little bit disrespectful unless the family have asked her to remove it
 
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In the UK it's now known as FII, fabricated induced illness. It's a tricky one, it's extremely rare although it might not be as rare as people think as many case go undetected/reported. If you take 100k children there wont even be 100 cases of FII as it is that rare. It's a really rare form of child abuse but a really serious form.

It's not a nice thing for any of us in the SEN community to accuse other parents of. A high proportion of parents are treated as though they are fabricating their childrens symptoms, for instance ASD parents trying to get a ASD diagnosis for their children are often parent blamed, told they are exagerratting their childs needs and abilities, behaviours are blamed on parenting or trying to get disability benefits. Its very rarely the case but its the go to thing for professionals who dont take into account how rare and unlikely it is to be the case.

FII is complex, it can be done for different reasons, most cases are done by the mother and usually because they enjoy being the caregiver and the attention/sympathy they get from others. There has also been cases of FII for financial gain, those who have fabricated or caused their child to become ill or to increase their childs needs and decrease their abilities, in order to claim disability benefits or raise money. This is really rare.

Most people think FII is done by a parent with children who are 100% fit and healthy, infact it can be either those with existing diagnoses or those with no health concerns at all.

Regardless of if Fii is the case here or not, this is the damage Kaytee is doing to the SEN community. People will be talking, looking at her actions and as she claims to be the voice of the sen community, people will start to wonder about others. Theres alot of SEN parents who give up fighting for assessments and diagnoses because of professionals judging them instead of listening and assessing the child first. If Kaytee is ever found to be FII the damage to the sen community could be horrific.

Whether FII is the case or not, without a doubt the professionals around them will be looking at FII being possible. She has created alot of attention around her so they will be viewing her page just like we do. They will 100% know more information than any of us do.

They will notice things we wont even notice. For instance if Kaytee has exaggerated or lied about meetings, assessments and decisions that have been made. They will know what attitude she has with professionals, how she acts in meetings, they may have reports off people who have reported her or raised concerns. There may be meetings and appointments that she has failed to attend. They will be concerned if communication with them is poor but she is constantly online. They will know about the fundraisers and will have noted the things she claimed she needed money for was funded and she never admitted that until weeks later once alot of money had been raised. There may be concerns raised by carers, we already know she was reported by one for coming home drunk and having a domestic. They will be concerned with why she doesnt disconnect his tube leading it to cause discomfort and increasing the risk of infection which increases the likelihood of hospital visits and admissions. She may have already been told about this which will concern them more if they are viewing her page and seeing she is still doing it. They will know shes aware missing meds and feeds can cause devastating consequences but she admits to doing it. The feeding school programme would have been another red flag because they will know GOSH advise ALL parents against this.

Each thing is a individual safeguarding concern, so collectively she is causing a huge safeguarding issue. As she has put her self into the public arena, there is no way they will overlook things in her case, and it wouldn't be the first or last time professionals got their own back for being made to look bad publically.

Without a doubt FII will be a concern for them that they have already noted and may be looking into. They have professionals dutys and I would not be shocked if they have raised quite a few safeguarding concerns. It's not for any of us to say if FII is the case here and people should be mindful that it is incredibly rare. But her own actions are questionable and professionals have a legal duty to act on concerns. If a professional even read this thread they would be duty bound to report safeguarding concerns. J should be on a CIN plan, if that has not been progressed to a child protection plan I would put money on it being progressed to that level soon.



Shes also removed the grid picture of her and her friend which seems odd to me and a little bit disrespectful unless the family have asked her to remove it

Thank you for this insight. Can I ask what’s a child protection plan and what would it involve?
 
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