My gorgeous boy, growing up fast
We saw the physio last week which was really positive. Physically he is now on the lower end of normal and she thinks he will be sitting on his own soon. We see her again in 3 months and then hopefully he will be discharged. On Wednesday we met up with the hv who was a bit negative and burst my bubble a little bit. She wants him to go to TOG and have more physio. She says he is very small for his age. I think he is doing really well. Putting him more upright in the buggy seems to have helped the puking or maybe it's more time spent at home now it's the holidays. Weigh in tomorrow. I think he's grown quite a bit but we'll see. I managed to get his milk delivered this week as well which has saved us several very long walks. Because of the nits on tuesday we had to cancel Malachi's appointment with Nicola so we will be seeing her again on 30th August.
My life with 5 children, all with special needs. 2 with mobility issues, 1 premmie with health issues, a cuddly miracle baby and an eccentric livewire on the spectrum
I'm Sophie, married to Simon and mum to Jeremiah (10), Isaac (8), Malachi (5), Ezekiel (3) and Zechariah (2). Also our 2 little ones in heaven, Eleanor (2005) and Elisha (2011).
Jeremiah has Autism.
Isaac has hypermobility syndrome/Ehlers Danlos type 3 and uses a wheelchair for anything other than very short distances.
Malachi has hypermobility and wears piedro boots to support his ankles
Ezekiel has a cleft palate, hydrocephalus, hypotonia and development delay
Zechariah was born with sepsis and has mild development delay.
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