Tag Archives: leyasjourney

Leya’s Journey Not for Profit Organisation

Sorry I haven’t updated much we have been busy getting settled in at home and just being a family again!! But I just wanted to do a quick update on the NFPO and what we are fundraising for. 

So Leya’s Journey is now all up and running as a not for profit organisation with its own bank account and paypal account. This basically means that we have a committee that oversee all of the fundraising events, can apply for grants and have control of the bank account. 

Leya

So what are our aims?? 

Our immediate aim of the group is to raise money to help Plymouth CHDU purchase 3 sets of sensory lights for use on the ward (currently they have 1 set between 4 beds).While Leya was in CHDU she was attached to loads of wires and monitors so it was impossible to move her and these lights were a godsend to keep her calm while she was having a coughing fit and to keep her occupied while me and Dan would take a break. We would love for the unit to be able to have one per bed so that the little ones do not have to share. We would also like to donate some money to the Plym unit where Leya had her operations. There is a waiting room for parents to sit and watch TV and also and area for the older children to play once they have recovered a little. This area is 100% dependable on donations to keep it running!

We also want to fund Makaton sign language lessons, firstly for Leya’s  immediate family but hopefully we will be able to have a pot of money so other parents/children in the community will also be able to learn! As Leya’s recovery is still a bit of an unknown we are unsure of what items she is going to need at this point. We know that she is going to need speech therapy in the future but she may face other problems when the tracheostomy is removed (including when this will actually happen). I will be keeping this blog as well as the fundraising page up to date so if things change and our goals change we will adapt our goals to help Leya in any way we can. 

But this is were we are dreaming big!! Our LONG term goal is to able to provide a place in Bude for disabled children to go, currently we have to travel a long way to attend groups, sensory sessions etc this is a hassle as the amount of equipment we have to take is a lot but also we are unable to travel with Leya alone so we need someone with us. I would love to have somewhere in Bude where parents could go without to much upheaval and where parents feel safe and happy for their children to attend. So we are going to dream big and see what we as a community can do!!

If anyone would like to raise money for Leya by taking part in a sponsored event, organising a fund raiser or just donating how ever much you can then please dont hesitate to contact the committee by email: leyasjourney@hotmail.com and we will forward a short application form to you.

You can keep up to date with Leya’s progress at her facebook page: https://www.facebook.com/Leyasjourney?ref=bookmarks

You can see how the fundraising is going and events being held at: https://www.facebook.com/groups/1428626847416602/

And you can donate via our paypal account: https://www.paypal.com/uk/cgi-bin/webscr?cmd=_flow&SESSION=cvyjuaZDWjsfi_JSVNokaderT6ICJco2Y5RfPUITqWJvGzptyvGOI8LeZlu&dispatch=5885d80a13c0db1f8e263663d3faee8d69a70501aadbc2ff6a1e7e8cc0df6b0b

Thank you in advance for any donations, events and help it is all greatly appreciated!!! 

Lots of Love 

Dan, Casey and Leya

Leya 2

 

 

Advertisements

Finally Some Good News and the Best News EVER!!

So where do I start these last few days have been emotional, amazing, confusing and basically a haze!!

So to start we had a NG tube put in so that Leya could have top up feeds and put weight on. So she is now on only high energy milk taking 120ml 5 times a day which is amazing and shows as she has put weight on and now weighs 11.5lbs!! This meant we needed to go shopping so our 16week old baby is finally out of tiny baby and newborn and into up to 1 month as 0-3 months is still far to big!!

20140723-110128-39688340.jpg
Daddy also came back to give me a break as I was physically and emotional shattered and Leya was so happy to see him, all smiles, giggles and snuggles!! And we also managed to get out of the ward when she was cleared of whooping cough but didn’t get far before she threw up all in her new pram yuck!!

20140723-110326-39806453.jpg

20140723-110328-39808031.jpg
This is where you have to listen carefully!! So if you follow Leya’s facebook page you know that she had a mini operation on Monday. For those of you who don’t know this was to remove a Granuloma and to check there wasn’t anymore! Well Leya was first on the list so she was fasted from 7.15am but didn’t actually go in till 4.30pm so was starving. She finally went in and came back out!! She didn’t come round very well, she was really unsettled which was unusually as this hadn’t happened the last 2 times.

We got back to the ward and she was really pale and clammy all night and her oxygen was rather low so she was on oxygen all night but seemed to pick up on Tuesday.

But the operation went well. She had a Granuloma just inside her throat which was removed and one just at the top of her stoma also removed!! They checked her food pipe to make sure that was ok and all was good then came the news that hit me and Dan like a tonne of bricks!!

HER VOCAL CORDS WERE MOVING!!! Cue the tears 😂 We couldn’t believe it in 1 month they had started to work and she can have the Trache taken out!! OMFG was this really happening. I was apprehensive and wanted them to wait a little longer to make sure all was ok but they put in a size smaller but unfortunately she couldn’t breathe with that one capped. Because Leya is small she needs a small Trache to let enough air pass for her to breathe if they cover it over. So the plan now is to let her grow for a while and then try again until enough air can pass and she is able to breathe on her own!!

But she wont have the Trache for life and for not much longer hopefully. My amazing trooper has managed to heal, grow and strengthen in 1 month and she will be having the Trache out as soon as she is big enough!!

20140723-110715-40035493.jpg
So with that exciting news she then decided it was time to start to try and roll over but hasn’t yet got the hang of it yet!!

20140723-110817-40097239.jpg
So keep an eye out for the next blog to see how Leya is doing and where we are in her journey that has a little longer to go!!

Love Dan, Casey and Leya xx

20140723-110934-40174259.jpg

Finally home….But only for 2 Days 😢

So as the title says we managed to get home on Monday YAY!! So we got the news that unfortunately it could take anything up to 2 months to get Leya’s humidifier sorted and we could stay until then (HELL NO was my answer) so we were sent home with extra nebulisers till this is to be sorted out!!
20140712-192730-70050772.jpg
So I rang mum (we didnt have the car because of the MOT fiasco!!) to ask her if she was busy and if she wasnt could she come and pick ALL 3 of us up 😃 commence the shouting down the phone!! At first she asked if I was lying then put me on speakerphone to tell Leya’s Great Grandad (g-dog) and her Uncle Kyle and Cameron to say they were happy was an understatement!!

So mum arrived and her and Dan took our things to the car (there was a lot after nearly a month of being in here) and of course there was no parking spaces near but in car park E the furthest away!! They filled the car then the waiting began….and carried on and on and then finally we got Leya’s 2 carrier bag full of medicines (I would like to state here that my daughter is not a avid drug user but they supplied us with two weeks worth 😜). So we could finally escape.

We got downstairs and I swear both myself and Leya hissed and started to burn when we came into the light (yes a vampire comparison) we had been in there for so long that the light (it was a dim day) was just far to much for our eyes!!

So we arrived home (sorry the picture is dark) to the family who couldn’t quite believe we were really home. Well Tieran the most as they didn’t tell him we were coming home so his face was the best 😁.

20140712-193448-70488290.jpg
Let the first night commence…all was back to normal Dan sleeping through the night and me not sleeping a wink just incase I missed Leya crying but once again our little piglet was fantastic and slept all the way through!!

20140712-193618-70578390.jpg

20140712-193617-70577158.jpg
So we were settling in, sorting out our new room, getting used to the equipment (your used to seeing it in hospital but its looks strange at home), teaching everyone how to care for Leya and the new sounds she makes all was good!!

20140712-194006-70806587.jpg

20140712-194005-70805001.jpg
Wednesday came and we went and spent the afternoon with our friends!! Which was amazing to catch up and see how much the not so little ones had grown!! Leya took a liking to Ethan and his arm which she decided tasted amazing.

20140712-193916-70756157.jpg

20140712-193917-70757395.jpg
So this is where the trouble starts. I take a walk to morrisons (in our new buggy which is amazeballs) to get some tea, Leya decides that she was to have a blue episode and stop breathing 😩 so I calmly suction her and helped her to calm down and she starts breathing again (i though I was going to have to do an emergency trache change) so i get home and she has another one not good. This is when the sinking feeling starts to occur, have they diagnosed the right thing, have we put her through all this for no reason??? So to be on the safe side we decide to change the Trache just in case its blocked. It was then we saw the Granuloma, for those of you who are thing WHAT THE HELL IS THAT?? It is basically Leya’s body trying to repair the hole that shouldn’t really be there, no biggy we put the new Trache in and called HDU to see what we had to do.

The ENT want to see Leya just to check all was ok, so of we went to Plymouth thinking we were heading for just a day out, how wrong was I.

20140712-194929-71369157.jpg
Leya was seen by the ENT team when she arrived, they cortarized the granuloma and gave us some steroid cream but this is when she decided to go blue TWICE in front of him. Bring in the Peds consultant… “We are not happy for Leya to return home we would like to observe her overnight”

Mum and Cameron left with the new pump (yes this is the day one of her suction pumps decide to break) this is when my daughter decided that in front of the nurse and just for fun she would have quite a few apnea episodes, go blue and drop her oxygen sats!! Que me feeling sick to my stomach with worry as to what is causing my little girl to struggling to breathe again. On goes the humidification and back to our second home of HDU.

20140712-195401-71641323.jpg
So bringing to story to a close we have been told we are back to square one, they think someone else is wrong but they are not sure what or where. She has had a chest X-ray which is clear, loads of blood test (i cried as it was a lot and her poor little hand is now bruised) and more tests to come.

Today she has been put on IV fluid as she has started to throw up her feeds again and has lost weight so she is dehydrated. We have been put into a cubicle as she has a viral infection (once again dont know what or where) which could be whooping cough so we have to be on the safe side.

So until we find out more or what is wrong with Leya and she has a had a prolonged period of keeping her oxygen up, not going blue and breathing all the time we will be staying in hospital. So as Dan worked out today our little poorly piglet has been in hospital for more than a third of her life already 😢

Oh and just to make life a little more exciting for us someone decided to reverse into our car and take the paint work and scratch our back bumper, just another think I need to be dealing with right now NOT!!!

So we are hoping that someone up there is willing to give us all a break and get us home again (for a long time) and let nothing else be wrong with our baby girl.

Lots of Love

Dan, Casey and Leya xxx

20140712-200440-72280599.jpg