Helenlight
New member
Hi,
Our daughter has been diagnosed with CF (no bloodwork yet), and has been given Vit A,C, and D (E still to come), Sodium Chloride, and now the enzymes with apple sauce. She's also currently on Augmentin and I've added an infant-friendly pro-biotic.
We've started to get the hang of syringing all except the enzymes into her mouth bit by bit, in-between her crying, it's not very nice, but she won't take a bottle yet and I put her to the breast afterwards and she's happy enough. But now we have the enzymes as well and she's not interested in the apple sauce and seems to hate the feel of the gritty enzymes. She won't swallow it, so I have been putting the mixture on my nipple when she feeds. This seems somewhat successful in that she swallows some of it, but she still hates it every time and I don't like the idea of breastfeeding being traumatic for her, because it was her 'safe place' before- the place she can be comfortable and secure and is our bonding time.
I'm finding it really hard (I've been really strong so far, through her hospital stay at 5 weeks, the ongoing cough and vomiting that comes from it), it just seems to be one thing after another. My partner is really helpful, but it is getting to him too. It's just so hard to see our once happy, thriving daughter, not only become affected by the CF, but become sad too. How do you all cope?
Thanks xx
Our daughter has been diagnosed with CF (no bloodwork yet), and has been given Vit A,C, and D (E still to come), Sodium Chloride, and now the enzymes with apple sauce. She's also currently on Augmentin and I've added an infant-friendly pro-biotic.
We've started to get the hang of syringing all except the enzymes into her mouth bit by bit, in-between her crying, it's not very nice, but she won't take a bottle yet and I put her to the breast afterwards and she's happy enough. But now we have the enzymes as well and she's not interested in the apple sauce and seems to hate the feel of the gritty enzymes. She won't swallow it, so I have been putting the mixture on my nipple when she feeds. This seems somewhat successful in that she swallows some of it, but she still hates it every time and I don't like the idea of breastfeeding being traumatic for her, because it was her 'safe place' before- the place she can be comfortable and secure and is our bonding time.
I'm finding it really hard (I've been really strong so far, through her hospital stay at 5 weeks, the ongoing cough and vomiting that comes from it), it just seems to be one thing after another. My partner is really helpful, but it is getting to him too. It's just so hard to see our once happy, thriving daughter, not only become affected by the CF, but become sad too. How do you all cope?
Thanks xx