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#teamhonk #goodwork #Ghana #comicrelief

Red Nose Day began on the 5th Feb, 25 years ago.  To mark the anniversary, Comic Relief wanted to show the progress in Africa and the difference that money raised has made, both here and in Africa.

To raise the awareness, 3 bloggers from our community are visiting four projects in Ghana on the 4th and 5th of February to see the difference the UK Red Nose money has made.

They will tweet and blog through their stay, and everyone can follow their progress as they go.

The 3 bloggers are:

They will visit the:

Virtuous Womens Bakery
Skilling women to bake breads, cakes and pies and establish an industry around it.

African Outreach
Agbobloshie with many inhabitants faces issues around sanitation and housing.  With the project, the community is being skilled to help themselves.

Vaccination Clinic
This speaks for itself.

Basic Needs UK Trust
Mental health problems in Ghana being addressed and helped to improve their lives.

All in all, it sounds like it will be a packed programme of events, and if you want to follow the chat, simply watch the #teamhonk hashtag for more information and to keep up with what the ladies are doing.  Bloggers are becoming more and more involved in world events and charity programmes.

We need to support each other as we work through the charity connections.

Best wishes to all in #teamhonk and a safe journey to you all.

If you want to follow their progress, simply click on the badge picture and it will take you to the blog about the adventure ahead.

x

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Christmas Delivery Dates Calendar

This is a thoughtful and helpful feature from Castle Cover.  They have built a delivery dates calendar for us all to use.

If you’re not sure when the Christmas Delivery Dates are, then just take a look at the interactive pages on their website and it will help you make the right decisions about those last-minute presents you are hoping to buy.

Clicking on the Delivery Calendar image takes you to their website, were you can check the last posting dates of different types of items and some high street stores.  Don’t waste any time as we are reaching the end of the road for buying our late goodies.

Castle Cover

 

 

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What would make Scotland the best place in the world to bring up children?

Becoming a parent was the unusual route for me.   My kids are all fast approaching teenagehood, but I didn’t give birth to them, and they don’t have my genes.

When we decided to keep the 3 little boys we had come to know, it was still hard to accept the amount of work that it was going to take bringing them into our lives, and to become a family instead of just a temporary home for them.

I’ve made more mistakes in my life since the boys arrived than I think I had ever made in my whole life before adoption.  Children change us, and I don’t think it’s always for the better.

My boys are getting older, and although we have managed to get this far, it’s been really tough, and it’s still tough going.

The lack of support is what blights our lives the most.  The lack of potential future care for my middle one eats me up at times, as I worry about who will bad use him, ala Castlebeck, or the other institutions that look after special needs adults.  I balance that with some of the most wonderful people I have ever met from charities, who spend valuable time with him and are the kind of people I hope are also in his future when we are gone.

Our Government needs to give parents and potential parents peace of mind.  I’m not sure that I have the confidence in that now.  For the future, I would like to see more consistent care and I’d like to see our children have “rights,” and not just pay lip service to it.

Our kids should be the focus for the future of the Scottish Government, but I have grave misgivings on that front.  I do think parents need more support from all angles, and especially special needs parents.  Perhaps I am being selfish in that respect, but I know I am not.

A friend and I both want spaces in after school clubs for our kids.  We both have special needs kids, and neither of us can get the cover so that we can go out and be full-time, useful members of society in a pubic place and working regular hours.  She works part-time, and I take on some work at home, but nothing like as much as I would like to.

There is no child care.

For Aberdeen, it seems that there are only 8 spaces per day for special needs after school care.  I have one day allocated and she has two.  We’d both love 5 days and to be able to earn more money to support our own families fully.  It’s never going to happen without support.

Those who call special needs parents a drain on society don’t seem to know that we’d love to be like them and get out and work for our own sanity.  Our culture and our Government won’t allow that, as funding options are always cut.  The only provision we have is a charity run one, which has limited resources.

I don’t think this is just a special needs issue either.  This isn’t just all about me and mine.

It’s about all our children and all our parenting experiences.  What could we do better as a society?  If we don’t tell them, or ask for what we need, it isn’t ever going to happen.

Being a parent is so important for the future of our country, but the support and the services just don’t seem to be there to prevent future long-term dependency.

The Scottish Government wants to make Scotland the best place in the world to bring up children, and so they have put together a National Parenting Strategy to provide better support for parents.

To help them plan the Strategy, they talked to over 1,500 parents about what’s best about being a parent, what they found difficult and what help they needed.  I think they need to hear more.

Many parents didn’t know where to go for help. Comments included “I didn’t know where to go or who to ask” and “I didn’t have family, I only had myself”.

Their comments tell us that we need to do more and do it better so that parents can find the help they need.

This Wednesday, on the 3rd October, the Scottish Government has decided to launch the Strategy at the Parenting across Scotland conference in Edinburgh.

Aileen Campbell, MSP, the Minister for Children and Young People, will be there, to talk about what Scottish Government plans to do to make sure that mums and dads get the help they need when they need it.

What help do you think mums and dads need?

What do you think would make Scotland the best place in the world to bring up children?

They would love to hear your thoughts.  Tell them your opinions using the Twitter hashtag  #pas12, and follow the chat on Wednesday there.   If you don’t want to contact them direct, leave a comment on this post, and I’ll pass it on.

If we don’t get involved, who will?

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Bloggers Saving Lives – Share Niger – Child 6 – Welcome Hapsatou

A warm welcome to Hapsatou from the Child 6 team, organised by @merrilyme to sponsor children for #shareniger on Twitter.

I’ve previously blogged about the campaign and the journey by Sian To to Niger earlier this year.  Read more here.

The campaign has so far managed to raise enough money to sponsor 11 children and help with the food crisis for the next year.  Most of us couldn’t afford to sponsor a whole child by ourselves, so we’ve done child shares, which World Vision UK has allowed, and the lives of 11 families and their villages will improve thanks to blogger power.

The Child 6 Team as it was, but who are now the Hapsatou team are @geekmummy @frugalfamily, @danielleGparker and I.

Didn’t we all do well….

 

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FREE Telecare Systems for Special Needs, Eldercare or Disability

This post isn’t one for bleating or winging about what some of us can’t get, or miss out on for our disabled or elder care families.  This one I am actually very pleased with and at the same time, massively surprised about as it seems to be UK wide, but at what levels I am not quite sure.

It started at parents night at middlers special school.  The alarm system man was there to show off the systems that can be used to help families who need to know what is happening through the night.

Imagine waking up by hearing a crying child who’d been kicked out of their bed.  Imagine hearing a noise downstairs and then investigating to find a child with front and back doors open and four burners of the gas turned on !!!!!  The potential is enormous for many parents of special needs children.  Our solution was to have one adult sleep downstairs permanently.

I had asked doctors, consultants, social workers and more for solutions to it, and the only answers I could get were to lock the doors so he couldn’t get downstairs, or put new doors on so that they could be locked.  I had visions of horror in the event of fire, or if something happened and the kids couldn’t get downstairs or out of the front door as the key is under my pillow.

Cutting a long story short, coming across these alarms is kind of bitter-sweet.  We’ve struggled for years, when there was a solution on our doorsteps, and one that the council also provides for free here.  The only charge is for things like elder care fall alerts at  £1.80 a week to link up to a call centre.

The equipment is free for us in Aberdeen, and it looks free from a lot of the local authorities I’ve had a look at.  I think Aberdeenshire is £4 month, but I think most people could stretch to that for peace of mind.

After persuading my mother that she needed an alert too after falling downstairs and making this mess of herself, she finally gave in to the fact that there needs to be some way of raising an alarm when I’m here as well as when I’m away.  I was two rooms away and had no idea she had fallen face first from the top to the bottom of the stairs.

The picture was 2 days after falling.  By 5 days, the bruising had joined up under her eyes and cheekbones.  The kids said that her bruises were “growing”.   Although she looks nowhere near her 77 years, she has arthritis which makes falling actually quite easy.  There were no broken bones which amazed me.

She has two pendants and a wrist watch style fall alert.  If she falls with the watch on, it automatically sends an alert to my wrist watch and to the care centre, just in case I don’t hear it.   She can use the pendants to either just get my attention, or to go to a call centre for help if I am not here.

We have a door alarm on middlers door which is actually quite small (wandering alert).  It goes to a unit which I keep beside my bed and wakes me up if his door is opened.  He doesn’t know how I know that he has left his room and I can usher him back to his bedroom and safety.

Alert Handset

In Aberdeen, they are raising awareness of the systems as too few people seem to know about them.  My first question was “how much will it cost”.  Sceptical as usual….    The equipment was installed within 2 weeks of my initial self referral.  An assessor came out to do an assessment of what would be needed, and two fitters came a mere few days later to install all the equipment.

The service was absolutely amazing, and I don’t say that lightly.

If you know someone who could benefit from peace of mind, let them know to look for it in their area.  They really are worth having and I have to say it again, I have been enormously impressed by the Aberdeen Telecare Information Service.

We’re sleeping easier and the wrecked lounge come bedroom is getting a makeover to celebrate it’s return to being solely a lounge.

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Urgent Appeal – Getting 7 year old Olivia Downie Home to the UK from Mexico

 

Update 27/6/12 – Olivia has flown back to the UK from Mexico.

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Update: Over £140,000 has been raised so far and the plane is on it’s way to get her.  Hopefully she is released from hospital in Tijuana and can come home with her family.

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This is Olivia.  She is 7 years old and she has neuroblastoma, which is a form of cancer.  She lives in Aberdeenshire in Scotland, so it is my neck of the woods.

SHE NEEDS OUR HELP TO GET HOME – Her parents are only allowed to spend 45 minutes a day with her in Mexico.

Could you imagine being in the position of having a very sick child who is stuck in a foreign country after taking a turn for the worse?  It might never happen to us, but it has happened to Olivia and her family.

She is now so gravely ill that she cannot be flown home on a chartered flight, and needs specialist help to get back as she is dying.   Her family can’t afford to get her home again, and there is a just giving page set up to enable them to raise enough cash to take Olivia home.

As at 4pm tonight, the fund is sitting at £79,000 and it needs to get to £110,000 to get her home.

If you have a few pounds to spare, please visit her just giving page at Olivia Downie Appeal. 

You can donate by text.  Text OLIV95 and your amount £1 –  £10 to 70070.

Head on over to the Appeal page and leave what you can and pass it on using one of the two twitter hashtags on the go #getoliviahome #bringoliviahome

Olivia hasn’t got long, I am hoping everyone can get her home.

If you don’t have the money to donate to the appeal, please tweet, facebook, digg, stumbleupon, reddit and more.

Don’t comment here, go and visit the just giving page.  Olivia Downie Appeal. 

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Bloggers Saving Lives – Help Us Sponsor Children for #shareniger

Who says bloggers don’t get anything done?  Well not us, that’s for sure, we do have blogger power.

Parent bloggers have raised enough for 6 children so far, and are on the way to 7 children in Niger for the next year.  Help us do more and expand the network willing to help.  Lots of us can’t justify the whole price at over £20 a month each, so the sponsorships are being gathered in a way that almost everyone can afford to join in with.

A subscription for anything from £1 gives us some to add to the pot, or even just a one of donation of whatever you can afford gives enough to sponsor a child for a year when it is added into the pot.  Some bloggers are doing a child share and for £6 a month, they are committing to 1/4 a child each.  Two children have just donated for 1/4 of a child.  How fabulous is that.

#ShareNiger came about when blogger Sian To went to West Africa and the Niger region with World Vision.  The trip was shared among our community by blogging and tweeting, and the media picked up on the stories.

How could anyone fail to be moved by the plight of this lady trying to keep her whole family alive on the pack of baby food she is given to feed just one child.

I know you need to know more.  I have pledged and paid for my 1/4, if you can pledge anything, a family will live a little easier in the Niger region.  Supported by World Vision, and with promises from the Government to pledge £1 for every £1 we raise, Sian and Merry Raymond are gathering bloggers together to sponsor children in the deprived area Sian visited.

If you can’t afford to give money towards sponsoring a child, you could help to do your bit by retweeting or blogging and helping raise awareness among your own online community.  For anyone who read this far, thank you for reading, and lets see us get to 10 children with the support of social media.

If you can join in, click here to sponsor a child in Niger.

Sian To –  Share Niger Story

Chris Mosler – Vaccines One Year On 

Merry Raymond – how to join us and sponsor a child in Niger.

 

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Robert Gordon University, Aberdeen. Best of British Show in aid of The ARCHIE Foundation – 25th May 2012

I’m happy to host this guest post from the fashion management students at my old Uni, The Robert Gordon University, who are raising money for The ARCHIE Foundation for children.

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Since it began in 2008 the annual charity fashion show at Robert Gordon University has raised tens of thousands of pounds for deserving charity foundations.

Now into its fifth year third-year fashion management students are hoping they can raise more money than ever before.

On the night of May 25th the Aberdeen Business School will be transformed on to accommodate 400 guests for what is hoped to be a marvelous and memorable evening of fashion, shopping and entertainment, with The ARCHIE Foundation being the sole beneficiary of the show.

This year’s show takes on the theme ‘Best of British’; rather fitting in the year of 2012 which sees both the Royal Jubilee and the London Olympic Games and plenty of patriotic celebrations along with them!

Catwalk themes including the British seaside, countryside, music, sport, people, designers, royals and the traditional tea party will showcase the very best of British style, and what’s more guests will be invited to enjoy a whole host of other entertainment on the night too.

Alongside the fashion catwalk there will be some fantastic on-stage performances and the opportunity to indulge in some of Britain’s finest foods and not to mention lashings of cocktails too!

Guests will have the chance to browse and buy within a unique shopping area dedicated to hosting a variety of local retailers; from fine wine to fashion there is something for everyone.  To add to the mix there will be a both a silent auction and a prize raffle on the night too.

With everything from cocktail mixology sessions to designer handbags, restaurant vouchers to fitness memberships, there are some fabulous prizes up for grabs and plenty of chances to win. With all proceeds going to The ARCHIE Foundation the students are determined to raise enough money to make a considerable contribution to the charity and its work.

As the official charity of the Royal Aberdeen Children’s Hospital, the Children’s Wards in Inverness and Elgin and Community based Child Health throughout Grampian, Highland, Orkney and Shetland, the ARCHIE Foundation is dedicated to making a difference to the lives of sick children through providing state of the art medical equipment, specialist staff, funding into research and of course lots of toys too!

The ARCHIE Foundation is so incredibly deserving of financial donations.  Its work really is invaluable to sick children and their families.

With the aim of surpassing last year’s total of £11,000 the third-year Fashion Management students have been up to all sorts in order to raise money in the lead up to the show. We’ve had our measuring scales and mixers out to host bake sales on campus, and we’ve put our creativity to the test too with kids’ crafts and face painting at the Bon Accord.

We’ll be proving our knowledge with a special Best Of British pub quiz, be doing supermarket bag packing and we’ve been out and about in the pubs and bars of Aberdeen promoting the show and collecting donations too all whilst planning what is sure to be the biggest night in Aberdeen’s fashion calendar.

The Best of British Fashion Show will be held on May 25th 2012 in Aberdeen Business School, Robert Gordon University, and Garthdee Road, Aberdeen.

Tickets for the show are priced at £15 each, or for VIP ticket priced at £25 guests will receive special goody bag, front row seats and access to the exclusive VIP room, and are available by contacting:

fashionshowrgu@gmail.com

We announce all of our exciting news and fundraising updates on Facebook and Twitter too:

Facebook

Twitter

We also have a Just Giving page where online donations to The ARCHIE Foundation can be made:

Donate to The ARCHIE Foundation

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Celebrities joined forces with Young Epilepsy to launch My Purple Pledge

Did you know that 112,000 young people in the UK are living with epilepsy?  Young epilepsy released a flagship campaign called “My Purple Pledge” this month, to help make a difference.  “My Purple Pledge” day was 26 March 2012,  and it was to build up for the international day to mark epilepsy awareness and National Epilepsy Awareness Week in May 2012.

Young epilepsy would like all of us to do something purple to help raise awareness of the condition.

Your something purple pledge could be:

  • Painting your toenails purple
  • Wearing a purple shirt or blouse.
  • Selling purple cakes.
  • Making purple toffee.

Anything purple can be count, no matter how small.

My Purple Pledge aims to raise money for the UK’s only dedicated charity for young people with epilepsy and other neurological conditions.

Lisa Farmer, Director of Fundraising at Young Epilepsy, commented: “My Purple Pledge is a fun way of generating awareness about a very serious condition.  All monies raised through the campaign will be used to provide life-changing support through our special school, college, medical centre and residential homes.  Ultimately, it will help young people with epilepsy across the country to fulfill their potential.”

Epilepsy is a serious debilitating disorder of the body’s nervous system causing symptoms such as paralysis, muscle weakness and seizures.  It affects around one child in every primary school and five in every secondary school.   Around 6,000 young people will experience communication, learning or behaviour problems. In some cases they will also have a significantly higher mortality rate.

The Children’s ISA is the main My Purple Pledge sponsor for 2012, with the first commercial partner being EasyLink UK, which provides epilepsy seizure monitors.

Please visit www.mypurplepledge.com for more information or follow My Purple Pledge on Twitter @purplepledge.  We may have missed the Purple Pledge official day for this year, but there will still be plenty of opportunities to get involved in fundraising for young people who need help.

Some Facts:

Around one in ten (6,000) experience severe communication, learning or behaviour problems due to their epilepsy.

  •  On average there is a child with epilepsy in every primary school and five in every secondary school.
  • There are around 600,000 people in the UK diagnosed with epilepsy.      That’s about one in every 131 people.   There are around 50 million people with epilepsy in the world. Around 75 people are diagnosed with epilepsy every day.

About epilepsy:

  • Epilepsy is a neurological condition – which means it affects the brain.
  • Epilepsy is described as the tendency to have seizures. Epilepsy is only diagnosed after the person has had more than one seizure.
  • Seizures are sometimes called ‘fits’ or ‘attacks’. Seizures happen when there is a sudden interruption in the way the brain normally works.
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Clic Sargent – A Yummy Grand Mummy

The CLIC Sargent Yummy Mummy Week is the 10th to 18th March 2012.   Anyone can join up and do something positive to help children with cancer.

This year, they are asking us to Do Something Yummy  and come up with new ways to raise money.  Click on the Yummy Mummy Link to join up and request an event pack.

Yummy Mummy is a fundraising campaign run by CLIC Sargent, the children’s cancer charity and for six years, mums in the UK have raised money to support the charity through the year.

Nickie @nickie72 From Typecast blog is one of the 4 Lead Blogggers on this campaign with Clic Sargent.  She has set writing prompts to help bloggers join in with promoting the campaign and spreading the word.  Visit her blog if you would like to take part.

I have chosen to do a Yummy Post as I do know someone who has had cancer and survived.

My mother is well into her seventies, although she certainly does not look it.  She was diagnosed with breast cancer a month after our boys came to stay with us.

It was difficult coping with three toddlers who had no boundaries at the same time as trying to help a mother who then had to go through treatment, surgery and the aftermath – while I tagged along three bundles of mischief.  It certainly brightened up the hospital ward.

She fought, and she fought hard.  The treatment was tough and the stay in hospital was tough.  She also had to contend with arthritis, thyroid disease, sciatica and is a type 1 diabetic.

The boys have been here for 8 years now, so the length of time she has been a survivor for is easy to remember.

It’s been hard going for her, so how difficult is it for a child to cope with?  We all need to help with local charities and get involved where we can.  I support a local charity with time already, and helping to spread the word about this scheme is an easy ask for me this week.

Nickie would love to see 50 link-ups for her writing prompts this week so please feel free to blog and link up with us on her blog on Thursday.

More Information

Yummy Mummy
Twibbon your Twitter avatar
Facebook page
#dosomethingyummy hashtag on Twitter

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Internet Safety Day & Online Games for Children

http://www.youtube.com/watch?v=cV1ZCF4oueQ

It was Internet safety day yesterday, and while I didn’t get to writing a post about it, I came across something that is aimed at children which worried me.

I am pretty vigilant with my boys lives online, which is probably a bit hypocritical considering how large my own online footprint is these days, but that probably makes me more aware of the possibilities.

My two had joined the growing army of young children who were playing Roblox.   I would ask that all parents whose young children use it to exercise caution.  Please research the reviews well and use the forums before you decide to allow your children to use it.  I would recommend that this site be used for over 16’s and possibly over 18’s.

Obviously it is up to each parent to decide what their children have access to online, but I would stress to do your homework around the online world style games offered to children.

When I first read the access request, I felt reassured that it was similar to the Penguin Club style interaction which keeps it safe for children, but it is very different indeed.

Moving on to the positive, there is a yearly campaign that helps promote safer use of the Internet among children and young adults.

This year they ran with the tagline:

“Connecting generations and educating each other, with the slogan: “Discover the digital world together… safely!”

This videos I have attached to this post are quite powerful.

Our children and young adults can be easily led.  We wouldn’t open our front doors to children and let strangers in, yet we don’t monitor our children enough online to ensure that they don’t open a portal to their safety bubble through the online world.

Be aware – check what your children are accessing, and who they are talking to.   Try it out for yourself when they ask for access to a new Internet game or craze as that is the only way you are going to know if it is age appropriate or not.

 

 

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Adoption Week Part 1. Not the Step Forward I’d Imagined

It has been adoption week this week, and as someone with three adopted children, I thought I should add my tuppenyworth to the discussion and share some of my “ranty wisdom”.  I will also do a jollier post later this week about more of the positives.

I felt like taking my remote control and throwing it at the TV when I began to see some of the coverage that adoption was getting this week.  The Cameron man on the telly moaning on about the process just got my back up, but that’s not unusual for me.

And to top it off, my hackles rose when I watched the segment about the woman complaining about the process and how long it takes to be assessed here, but who had plenty of dosh and managed to find the readies to go abroad and adopt the youngster she wanted.

Now don’t get me wrong, I would have gone abroad if I hadn’t managed to find my forever children in the UK, but come on, complaining about the system you have to follow to get those children is just plain wrong if you don’t even adopt from here.

Let me tell you about how the adoption process was before they made it that little bit tougher.  We went overnight from no children to 3 children who were not fully socialised.  Foetal alcohol babies are hard work, I can tell ya.  Imagine your trouble with a crying baby with colic who doesn’t sleep, and multiply that by a factor of 1000 x 1000 with knobs on and that could be the potential.

All those wannabe mums out there think that a little bit of love is going to make it all right – well it doesn’t.  Those cute little bundles may very well end up as aggressive, troubled tots who don’t get the help they need to survive.  Lots of families disrupt, even now when they can’t cope with the changes that children with high needs means.

Make no mistake, if you have a diagnosis of Autism, or an “acceptable” condition, the world will sympathise and help you with your children.  If your children have a diagnosis of Foetal Alcohol Syndrome or your child is Drug affected, you are going to hit your head up against a brick wall to get help.  And if you do say what the diagnosis is, people will think you are a raving alcoholic and start crossing the street and avoiding your kids party invites.

The bottom line is that most of the young children in care nowadays are disabled, alcohol or drug related births.  There are some who are orphans or young mums not wanting the responsibility, but they are certainly not the norm, and potential parents HAVE to get it through their heads that love is NOT enough to bring up drug and alcohol affected children.

I HATED the adoption process.  With an enormous passion.  I thought it was too long and I thought it was ridiculously monotonous and repetitive, but the authorities HAVE to try to suss out as many of the nutters who try to adopt for other reasons as they can.  If they handed over kids to a ring of child abusers, we would all be up in arms that the process wasn’t comprehensive enough.

Lets get down to the nitty gritty.  Adoptions take so long because there is NOT ENOUGH MONEY in the pot to get the work done that needs to be done to keep everyone safe.   Social workers have too many groups to assess, and to be frank, lots of approved adoptive parents sit waiting for the phone to ring rather than being pro-active and finding their future kids across the country.  There are also some fabulous homes not being used because there are not enough staff to get the meetings set up, organised, pulled together and finalised.

I do think the inflated considerations about race and ethnic backgrounds are pretty crap to be honest.  Lets just chuck kids into uncontrolled and often violent childrens homes eg just because they might be black and christian and a council only has white protestant adoptive parents on their books.

If I get the religions wrong, I apologise – as being a non-believer I just don’t care what religion anyone else is as long as they don’t try to sell me their faith.  That doesn’t mean I wouldn’t happily support a child who needed to learn more about their own faith and culture.

I’d like to see the kids put into homes that will stick with them through thick and thin, support their race and ethnic backgrounds, and to hell with the rules of what colour skin, race or nationality we should be before we can help a child escape from institutionalisation, temporary parents and abusive homes.

After care is rubbish.  Yes, there are “supposed rights” but considering post adoptive care says there is no money in the pot to provide anything, then it really is an empty promise unless it is desperate in my experience.

I am afraid that the negativity far outweighed the positivity that it should have showed, and would put people off finding out more, or moving forward with a process that needs to be shored up.

Right down to basics, adoption is about being parents.   In the same way that parents take on responsibility for children and have to fight for their needs, there is nothing different.    There is no special treatment in being an adopter once you are there so think about it long and hard, and treasure the preparation process because it is there for a reason.

If Mr Cameron wants to make the system work, stop complaining and support the Councils who are mostly doing their best with the means they have at their disposal (money, people and imposed rules) and ringfence pots of money for adoption and disability.

Yes, there are problems and yes, there are always nasty people who don’t do their jobs right, or get in the way of things happening, but they are in the minority.

I saw those segments, and rather than feel good about what was being said, I was conscious that if I were a new potential adopter, that it would massively put me off if I thought that the system was as difficult to breach as it sounded.

Mr Cameron needs to put his money where his mouth is to find alternative methods of moving adopters through the system and helping approve positive matches for families with support to help families cope with the potential problems they will face.

I’ve said my piece and now I will settle back and sort out my three adopted boys photos for christmas cards.   The whole process was worth every rotten moment it took to get through.