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Re: Re: Children after PMG child

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Food for thought..............if you do decide to get pregnant again start

taking prenatal vitamins now.

Just to help make sure of no neuro tube defects.

Good luck in your decision!

Donna

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Hi all! My son was born 11/11/01, and 06/02, we found out he

had PMG. I had gotten pregnant with my daughter Emma in 05/02/ So I

was about a month along when we found out about . She was born

at 35 weeks, and after her ordeal, we had her brain scanned. And

everything looked normal. But until then we pretty much held our

breath. She is now going through these terrible 3's. UGH. I want

to pull my hair out!!! ANyway, as hard as it has been on me having

them so close, and him not able to walk. It has been great for

. He wants to do everything she does, and is very interested in

what she does. Hope this sheds some light.

Dianna

11/11/01, BPP

Emma 12/04/02

Re: Children after PMG child

To: polymicrogyria

<span><p><span><p>

That is a great idea and it certainly could nothurt<BR>

<BR>

<BR>

& gt;<BR>

& gt; Food for thought..............if you do decide to get pregnant

again <BR>

start <BR>

& gt; taking prenatal vitamins now.<BR>

& gt; Just to help make sure of no neuro tube defects.<BR>

& gt; <BR>

& gt; Good luck in your decision!<BR>

& gt; <BR>

& gt; Donna<BR>

& gt;<BR>

<BR>

<BR>

<BR>

<BR>

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<br><br>

<div style= " width:500px; text-align:right; margin-bottom:1px;

color:#909090; " >

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I won't lie to you it is hard work having a special needs child

> and a

> new baby, I applaud some of the parents who have posted on here

> who have

> 3, 4 and 5 additional children - I really don't know how you do it !

> The only thing I can liken it to is having two babies, twins if you

> like, but it is so rewarding when they sit and smile, laugh and

babble

> at each other, there was some jealousy to start with (as with any

> siblings) but they really do show affection for each other now.

I really felt like I had twins. was born in Nov, and Emma the

following Dec. They are 12 months and 23 days apart. It was harder

than heck to say the least, Emma didn't walk til 16 months. UGH. But

now I wouldn't trade it for any other way. wants to do

everything she does, what an incentive for him. And he wwill always

have a friend on HIS side.

Dianna

Re: Children after PMG child

To: polymicrogyria

> *** Before acting on this email or opening any attachment you are

> advised to read the Eversheds disclaimer at the end of this email ***

>

> My son Dylan (3 years old) has PMG and epilepsy and we have

> recently had

> another child who is now 6 months old. We agonised over

> whether to

> have another child, but after having been told by our geneticist

> that it

> was highly unlikely that it would happen again we decided to go

> for it.

> I was very carefully monitored by the maternity unit at our hospital

> they gave me an ultrasound scan every 4 weeks up to 30 weeks and also

> carried out 2 mri scans to check the baby's brain. They could never

> give a 100% guarantee that he wouldn't be affected but thankfully

> everything turned out ok.

> I won't lie to you it is hard work having a special needs child

> and a

> new baby, I applaud some of the parents who have posted on here

> who have

> 3, 4 and 5 additional children - I really don't know how you do it !

> The only thing I can liken it to is having two babies, twins if you

> like, but it is so rewarding when they sit and smile, laugh and

babble

> at each other, there was some jealousy to start with (as with any

> siblings) but they really do show affection for each other now.

> Dylan - PMG and epilepsy - 3 yrs old

> Solihull, England, UK

>

> Jo

> Secretary to Charlotte Digby,

> & Pringle

> Commercial Litigation - Eversheds - Birmingham

>

> Direct Dial : +44 (0)

> Direct Fax : +44 (0)

> Email : joanneErobinson@...

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>

>

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