主题:【文摘】一场正在围绕小女婴展开的公共事件 -- 酥油茶
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vmelove (2 days ago) Show Hide
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My little boy was born with imperforate anus and since he had surgery at a couple of days old, we've been dilating him for 4.5 months now.
I've found a very good support group on facebook if anyone is interested - "imperforate anus support group"
sophiedumighan (1 week ago) Show Hide
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hi my daughter was born with this which went undetected for 3 weeks she had the op which went well but now she is 5 and she can not control her bowel which is really upsetting as she is at school now and the other children are picking up on it she is on the waiting list for the ace op. which she will have a little hole in her belly where we can do wash out through which she will need for life as the doctor said her anus cant contracted because it was made for her
CPower84 (4 months ago) Show Hide
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Why are you smiling, Sir? You are talking about innocent, sick babies.
Show a little more sensitivity, please.
SectorClear (3 months ago) Show Hide
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It seems like the language and voice tone he uses is meant to give hope and to not scare the parents.
If your baby had this, would you want your doctor to sound hopeful or troubled?
nacha86 (1 year ago) Show Hide
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My daughter was born with a imperforate anus but with a fistula and 3 days after birth she had surgery. right now she is 3 months old and one a day i have to dilate her till she turns 1 yr old. i want to ask you mommys if your baby is a year old or older is there any complication with your babys bowel movements?
oceanna20 (1 year ago) Show Hide
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My daughter was born with this, bladder problems, renal failure and lower spinal problems. She is 5 this year and has a colostomy 4 life and she has bladder incontince. She is due 2 have a kidney transplant in the near future and bladder reconstruction. She indured many many oporations and has many 2 come. Shes a remarkable and stunning little girl. and im so lucky 2 have this little miracle.
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Amber14544ht (1 year ago) Show Hide
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FREESEXYPORNSTARS . net_
You S U C K
Caperfae (1 year ago) Show Hide
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My daughter was born with this.
Her corrective surgery was when she was 3 weeks old.
She didn't need a colostomy as the surgeon was able to find a fistula while in the NICU after delivery .. which we had to dilate a couple of times a day using Hegar dilators until her surgery.
Post surgery her anal opening had to be dilated until she was about 1 year old using the Hegar dilators and the circumference increased as the months passed.
Neicy2 (1 year ago) Show Hide
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My son was born with the same exact thing and we also had to dilate him twice a day till his surgery at 6 months then again after the surgery till he was 10 months. He is doing great now at 17 months old.
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无肛症有很高的可能和心脏、肾脏的异常结合,但是除了极严重的情况,孩子会在手术后正常的发展。
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