I took Kaden back to the doctor on Thursday as he'd been fevered and coughing all night Wednesday.The doctor checked him over and said he heard something in his chest and because of his history he would give Kaden an antibiotic for a weeks course and to also keep giving Kaden calpol to keep his temperature down.
Since Thursday Kaden has been up and down,he follows me round the house saying hug..hug all day long.I hate to see him so miserable.Every night Kaden cant get slept for coughing and the last 2 nights i've switched off his pump during the night as he's being sick with coughing.
Tonight we are all having a early night with the hope of getting some sleep - although we better get used to sleepless nights as its only 6 weeks until baby brown appears!!
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'Our Wee Man'
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'Kadens Journey'
This about our unborn son Kaden who was diagnosed with a diaphragmatic hernia known as CDH while in my womb at 18 weeks.After hearing about the condition and all possible outcomes we decided to give our baby the best chance in life.The doctors gave him a 50/50 chance of survival.Knowing our unborn baby had a long fight ahead we picked a name for him with a meaning - Kaden means ;fighter and he did exactly that.At 37 weeks gestation we had a MRI scan to find most of our babys organs were in his chest - his stomach,spleen,left lobe of his liver,bowel and intestines.At 39+1 weeks Kaden was born by c-section on Wednesday 25th July 2007.Kaden was operated on at day2 to have his organs put back where they belong.After an emotional 6 weeks of which Kaden spent 4 weeks in intensive care and a further 2 weeks in the Neo-natal.
Kaden was allowed home on the Wednesday 5th September 2007.
Kaden has had 4 operations in all - 1 lifesaving op at day 2,1 fundo and gastrostomy and 2 hernia repairs.
Although Kaden has feeding issues - we are so proud of 'Our Special Little Boy'who continues to thrive every day.And we are so Thankful to have 'Our miracle'.
Kaden was allowed home on the Wednesday 5th September 2007.
Kaden has had 4 operations in all - 1 lifesaving op at day 2,1 fundo and gastrostomy and 2 hernia repairs.
Although Kaden has feeding issues - we are so proud of 'Our Special Little Boy'who continues to thrive every day.And we are so Thankful to have 'Our miracle'.
Cdh support - Cherubs
CDH - Babies
If you want to email me my email address is:-
gil.brown@talktalk.net
About Me
- Gillian Brown
- Full time mum of four cherished children Brooke 13, Regan 11 and of course our special son Kaden 'The Fighter', 2 and baby jaxon born in April and beyond doubt my wonderful husband Mike.
' Kaden '
'Our Wee Man'
1 comment:
I hope Kaden starts to feel better very soon!! I loved the photo of him sleeping on the treadmill!
Vicki
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