CHILDHHOOD CANCER AWARENESS MONTH!

Deqlan Ross Higgins - Cancer Survivor

Declan Du Toit - Brave little Angel

Hi All,





For those of you that do not know - September is childhood cancer awareness month. My dear friend Samm is honouring a warrior, angel or survivor of cancer each day and I would like to follow her example by honouring these children.





I am going to be dedicating the entire month to two very dear children that are very close to my heart:





Declan Du Toit - Angel



I followed Declan's journey by reading his blog from when he was diagnosed with cancer at a very young age and continued to follow until now, even though Declan is no longer with us, he lives on in spirit guiding everyone to do good work in his remembrance. Please go read Declan's story and go and see what his parents are doing in his memory on www.all-hands-on-dec.co.za



I was and still am amazed at the strength of a small baby, Declan had unbelievable courage and fight in him. Although Declan is sorely missed by many, he lived his purpose and left a huge imprint on everyones life. The most gorgeous little baby with the most wise eyes!



This month we thank the Lord for allowing us to be part of Declan's life and to follow his story.. We remember and honour Declan this month.



Deqlan Ross Higgins - Survivor



What more can one say about a Brave little boy! Deqlan was diagnosed with cancer round 8 months old and he fought a avery brave fight - he was determined to beat cancer and he did. I followed his story every step of the way and continue to follow his story as he goes full steam ahead, with the help of his wonderful family, to overcome his Autism. Deqlan ahs made wonderful progress and I urge you all to read his story on www.deqlanhiggins.blogspot.com



Deqlan, we are so proud of you and we can see all the strength and determination in your eyes - you are here for a divine purpose and I can't wait to see you grow up and fulfill that purpose. You have a very special place in my heart always and forever!



This month we thank the Lord for Deqlan and his continued health, we also honour you Brave Deqlan!





We also think of and continue to pray for all those little ones fighting this horrible monster. We pray that the Lord holds them in palm of His hands and heals them. We also think of and pray for all the families who have lost children to this horrible monster!



Lets stand together and create awareness for Childhood cancer!



Love

Claire

Happy Brithday Ethan!

Ethan making his entrance a year ago!
Mommy finally meeting Ethan!

Sleeping in his hospital cot - so peaceful!

Ethan at 1 year!

Happy birthday big boy!

To Our Gorgeous Baby Boy!

Time has passed by so quickly and you are growing so fast. I can remember your birth day so clear, it was a cold day, storms everywhere - there had to be big events happening beacuse the most special little boy was going to be born. I was so excited to meet you and I was so happy to see your tiny face all safe and sound once Dr Miems finally got you out!

There is never a day that you don't smile - when I walk throurgh the door everydasy after a long hard day, you are so excited to see me and smile from ear to ear.. What more could a mother ask for....

We love you so much and wish only the best for you.. We love you tons and tons. God bless and keep you safe our precious baby boy!

Love

Mommy, Daddy and Hannah

Quick Update!

Hi All,

Hope you are all well? Its been a long time since I wrote an update and thought I would quickly update you on the happenings...

My babies are doing well. Hannah has almost completely recovered from Bells Palsy and her face is almost 100% back to normal... Hannah is busy recovering from Bronchiolitis and is full of life and energy.. Ethan is trying very hard to stand for longer than 2 sec's and is doing so well. Can't believe he will be 1 in less than 2 weeks time, he has grown up so quickly!

Furthermore, we are getting ready to move - yes again... But my gut feel tells me this move is going to be good for us. So I am packing and getting everything ready and sorted for the big move next weekend..

Its Vanessa's wedding on Saturday, looking forward to that....

Have a great weekend everyone..

Lots of love
Claire

Peace Of Mind.......

Hi All,

Hope everyone is well and keeping warm.... I can't wait for summer to arrive.... The smell of summer rain, summer braais and wearing less clothes... Also the joy in watching my children enjoy the outdoors and splash in water , just having fun.. They are so irritated by staying indoors most of the time cause its so cold...

We had Hannah at the paediatrician this morning just for a second opinion and to just make sure there is nothing else causing the paralysis in her face and because we have seen no change since she started all the meds.. The paed does not seem extremely worried, he checked her from top to toe and said all looks good except for the paralysis in the face. He put her on stronger meds and said we should wait a week and come back, if there is absolutely no change, he will then insist on an MRI Scan and blood work.. We are positive that it won't come to that and that we are going to see big change...

Hannah is 2yrs 7months today.. She is growing so quickly and learning so much.. She basically says everything you say, so we are very careful what we and others say around her.. Its amazing how they learn a persons tricks and sayings...

Anyway have a great day and thank you for all the prayers for Hannah, I just know they are working..

Love
Claire

Bell's Palsy???

Hi All,

Hope everyone had a good weekend with your loved ones and friends....

We had a pretty eventful and very stressful start to our weekend....

It all started when I got home on Friday afternoon after work.. I walked into 2 smiling children except there was something wrong with Hannah's smile... Her smile was just not the same smile and I just took a deep breath and sat down on the couch and kept saying to her " look at mommy", "smile for mommy"... It looked as though the entire right side of her face had no emotion and was not responding when she smiled or cried or spoke... My heart sank right to my feet and I started to panic... I was almost sure I was seeing things but my gut instinct was telling me there is something wrong!

My aunt was on her way to me and I thought I would just wait for her to get to me and see if she see's the same... I called Stephan and he said I must just wait till he gets home and he will check her face but he said he is sure its nothing!! My aunt walked thorugh the door and took one look at Hannah and said she see's exactly the same thing!! Now, I was really worried, I loaded Hannah and Ethan in the car and off we went to the doctor...

We finally saw the doctor and all he said was that she has Bells Palsy.... Huh, what is that!! Well, its a tempory facial paralysis that is caused by a virus that attacks the facial nerve and causes damage... Sounds scary!! The paed says the prognosis in children is very good but its very rare to see Bells Palsy in a child Hannah's age.. The doctor does not seem as worried as Stephan and I though! He said we must give it till Thursday and if we see now change by then, he will draw blood and start all the big scans etc, to make sure there is no underlying problems!

All I ask is for prayers that Hannah recovers full and quickly and that there are no other underlying issues.. We are very positive that she will recover nicely and that this is just merely a bump in the road!


God Bless..

Lost of love
Claire

Declan Day

DECLAN DU TOIT - The Inspiration

Stephan, Me, Simon & Gillian

Pet & Caelum

Nadine, Fabienne & Isabella

Liesel doing face painting - I think Liesel did a great job!

Fern and Amy - what a cute baby girl! I loved holding her...

Liesel and Me

Precious Aiden - Kim's little one



Hi All,

Hope everyone is keeping warm in this very cold weather we are having.. I definately think winter has finally arrived..

What an awesome weekend we had, especially on Sunday..

Sunday was an extra special day, it was Declan Day! Stephan and I are part of a charity called All Hands On Dec Friends, inspired by the brave Declan Du Toit, which fought so hard and lost his battle to cancer on 8 February 2009..

So many people came out in the cold to show their support and love they have for this brave little soul and to do a little to help save lives. There were over 60 new Stem Cell Bone Marrow donors and over 60 pints of blood donated.


You could just see Declan smiling down on Gillian & Daryl..


Gill & daryl, what an amazing day it was.. A day to honour your son! It was perfect in so many ways.. Your dedication and love shows and your bravery shines so bright.. Thank you for giving us the opportunity to be part of All Hands On Dec Friends.. Its an honour and privillage!


See pictures above of Declan Day! Everyone was smiling, just like Declan did..

God Bless and Keep you all safe!

Love
Claire

This is why.....

Hi All,

Samm sent me pictures of the Scrub a dub dub handout at Kalefong hospital and I am so glad she did.. I know that there is a lot of you that don't understand why I do what I do!! I don't have kids with cancer so how on earth can I possibly care so deeply for these other kids battling the disease?? This question is asked to me over and over again...

Well, I care so incredibly much because these kids are so very brave.. Braver than any adult I have ever known.. They endure so much... I want to make a difference, be it a small one, at least I know I have tried.. I love children and love seeing them smile and be happy..

I could carry on, but have a look at these pictures and then you will see why I do what I do!! Why I care so much... Have a look at the sparkle in their eyes, have a look at the moments happiness just a few simple things bring, that we take for granted everyday.. Maybe then you will understand!

Lots of love

Claire