Coming home was great, tried to breast-feed Poppy, I had enough milk to feed the whole of a maternity wing, but was she interested? No! I decided long before that there was no point in getting stressed over it. Just go to Mothercare and buy some bottles - "easy". Unfortunately not. The feeding became increasingly harder to do - one ounce here, ½ an ounce an hour later. Very itsy bitsy. Alarm bells started to ring for me. Unfortunately not for anyone else. When I took her to be weighed they said, "Maybe that's the way she is", or "Oh well, we can't all have a healthy appetite". Being a bit more suspicious of my daughter's inability to consume any quantity of milk, I asked to see the doctors. Looking disgusted they made me an emergency appointment.

Telling the doctor all my concerns, and her looking blankly back at me, and probably thinking 'the anxious mother line'. She listened to Poppy's heart, and her attitude changed, "I think you should go to the hospital." Relieved and in tears I phoned John (Poppy's Dad) She was diagnosed with a VSD - and sent for lots of test. Luckily it didn't require surgery at that moment, might still do in time. I was so happy, I know that sounds strange, at least I knew why she was feeding so poorly...

Back to the consultant at the hospital, to be told that wouldn't cause the feeding problems that we were experiencing. I heart broken. What was it then?

On seeing the orthopaedic consultant, Poppy was put in a frame, making the next 15 weeks very difficult, but through it all she was growing in to a beautiful, happy girl. And the bond, though very strong at birth was becoming increasingly stronger.

The consultant at the hospital, at my request, had a scan of her kidneys done, my worry was that it is hereditary on John's side to have polysistc kidneys. I waited for the results, the consultant said there was only one kidney!!

In shock and baffled by what they were telling me - they said there were too many underlying problems and they wanted to do a chromosome test. The results would take 6 weeks to come through. They would refer me to a dietician in the meantime and do more tests on her kidneys.

In the meantime things had been hectic, we were moving house, and the phone call came, the consultant wanted to see us at the hospital. I knew the results had come back. But it was the day I was supposed to move - what a disaster! We went to the hospital at 10 am. It was like the firing line. Two consultants were there to meet us. I knew (mother's intuition) that the results were bad. I originally thought that it was cerebral palsy as she had a weaker side and the development, physically, was delayed. But sitting there, they handed me a bit of paper with:

"22q11.2 deletion

DiGeorge Syndrome"

It was like a foreign language. I'd never had, or needed to know of, anything like this before. One of the consultants said, "I think I'll remember this forever. We're so sorry. We should have listened. Sometimes mothers know best." The tears started falling and didn't stop for about a week. The people who moved out of our new house must have thought I had really lost it, there was me in floods of tears.

Poppy is now 20 and our only child at home . The other four have flown the nest . Married and we have seven  beautiful  grandchildren between  them .

Poppy has had many issues  in that time, but still continues  to be a beautiful kind caring young lady .

At 3 years old then again at 5  Poppy had a phlangoplasty to correct nasal speech . The two surgeries together have been a complete success .At this time Poppy also had gromments on several occasions , this was not a success , so poppy wore  hearing aids till the age of 12. And continued with several  years of speech therapy.

The other issues have been diagnosis of sensory processing disorder , separation anxiety and Autism.

Poppy showed signs of mental health  issues at about 10 years old by the age of 12 we were under camhs and medicated .Unfortunately  when Poppy was 14 she lost her maternal grandfather .Due to the situation i moved in with my mum and nursed my Dad until the end . But this meant i couldnt be poppys full support . This contributed in Poppy having a breakdown  and was hospitalised in Great Ormond street for 8 weeks . 

This illness unfortunately triggered further  diagnosis of chronic fatigue syndrome and fibromyalgia.  This has been  extremely hard to diagnose as Poppy is selectively mute and couldnt explain the constant pain and extreme fatigue. This has been so heartbreaking and I've watch the mental health and medical symptoms   change our daughter into a young lady that struggles to go out of the house, and slowly takes a little bit more of her .

We have been very  lucky to have had excellent adult mental health care  with the crisis time being involved on many occasions .we currently  are under psychiatrist psychologist and severe pain team.

On education Poppy has always attended  at special needs school and continued  that post 16 at a special needs college that  specialised in mental health and Autism. 

 Now after 3 years we are starting a new venture of a day centre mainly participating in art activities . Poppy is being funded for two morning a week this is because Poppy struggles with activities due to being in so much pain.We also receive a  social package. 

 I feel like i should list Poppys diagnosis i feel that  all fall under the bigger umbrella of Di George syndrome .

22q11, Autism, Sensory processing, Selectively mute, VSD, Migraines, Missing rib on left side, Missing kidney left side, Cleft in t6 vertebrae, Chronic fatigue syndrome, Fibromyalgia, Mental health issues, Severe anxiety, Severe pain, Compromised immune system, Hypomobility, Scoliosis. 

I feel like I’ve missed chunks of time in this update . But believe me this has been a journey with lots of twists  and turns  . Lots of tears and lots  of laughter .

Our 22q journey keeps giving and throws up some curve balls at time. We continue  to fight and embrace our journey.

On reflection Poppy has given us so much joy as parents .And  continues to teach  us so many different  skills, we tackle every one with positivity .

We have met some truly remarkable people and life long friends .

To all you parents of newly diagnosed children i would like to say  that this journey you are venturing  on will test you to your limits , will test you patience knowledge and let you acknowledge skills you never knew you had . Seek advice and support  from parents  that have  gone before you . Its a beautiful journey  and the smile on your childs face at the end of the day makes  its so much easier .