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Re: mito and miscarraiges

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I also have had 2 miscarriages, but am thought to be free of mito and am

relatively healthy. LOL

My oldest daughter (8yo) is healthy, followed by first miscarriage at 9

weeks, second miscarriage at 19 weeks(we did do chromosome studies this

time, came back totally normal 46 X,Y), then came Gracie, 3yo, (with

who knows what kind of something going on), and then 13 months later

came Matty (Pearsons syndrome and Kearns-Sayre syndrome).

Sorry a little late in responding to this thread. I also had 2 miscarriages. My son Jake will be 8 in April and now undergoing extrensive work-up do the the fact that they think he may be mildly effected with the same mito disorder as Clayton. After Jake I got pregnant when he was 9 months old. I lost that baby at 26 weeks - due to a placental abruption - she was stillborn. I am told that she was healthy - or at least no chromosomal damage. After the fact I was found to have a high ANA and anticardio lipobodies (I think that is the name) and thus with my next pregnancy - the twins I was on heparin, baby aspirin and predisone. Well actually between the twins and Jake - and very early - before I started the regimn above - I lost one at 6 weeks. They do not know why. After that I carried the twins to 34 weeks - but very difficult pregnancy - and also they did see lots of problems with clayton throughout the whole pregnancy.

Well Clayton was diagnosed with mito - complex I in April of 1999 and now we are having a work up on Jake. Clayton's twin Cole seems to be ok.

Love,

Sharon

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In a message dated 02/14/2001 5:44:24 PM Eastern Standard Time,

lawblond7@... writes:

<< Sorry a little late in responding to this thread. I also had 2

miscarriages.

My son Jake will be 8 in April and now undergoing extrensive work-up do the

the fact that they think he may be mildly effected with the same mito

disorder as Clayton. After Jake I got pregnant when he was 9 months old. I

lost that baby at 26 weeks - due to a placental abruption - she was

stillborn >>

I have been wanting to respond to this also. I had endometriosis, diagnosed

at 19 years old. I had an ovarian cystectomy in 1994 and after one month of

pergonal I became pregnant. I had a partial placenta abruption at 33 weeks

with Nolan and delivered him at 35 weeks weighing 6 lbs 9oz. I am wondering

if any of these signs were early signs of mito.

Additionally, Nolan was hypoglycemic and jaundiced (9 days under lights), at

5 weeks had bronchiolitis and at 3 months had severe colitis.

Michele

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had an ovarian cystectomy in 1994 and after one month of pergonal I became pregnant. I had a partial placenta abruption at 33 weeks with Nolan and delivered him at 35 weeks weighing 6 lbs 9oz. I am wondering if any of these signs were early signs of mito.

Additionally, Nolan was hypoglycemic and jaundiced (9 days under lights), at 5 weeks had bronchiolitis and at 3 months had severe colitis.

I also needed pergonal to become pregnant with the twins - this is after Jake and after the stillborn and the miscarriage. I could then not get pregnant- but after one month on perganol I got pregnant with twins - VERY HIGH RISK.

I also had endrometriosis and also had to have my left ovary removed after the twins as I had a pound and a half ovarian cyst and that needed to be removed and crushed my ovary. Twns were born at 34 weeks - clay was 4.4 and cole 5.5. Clay initially had problems maintaining his body temop and was also hypoglycemic and slightly jaundiced. He aspirated at 6 days due to reflux and was placed on a monitor. As for me I had to have my gall bladder removed 8 weeks after the twins. I am now remarried and thinking of having one more child - but obviously I am scared.

Love,

Sharon

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It's my understanding that if the foetus get a lot of the bad mitochondrias,

it can't live, and the result is miscarrige.

I've had one, my mother had one, my maternal grandmother had several ...

Ingvild

>From: lawblond7@...

>Reply-To: Mito

>To: Mito

>Subject: Re: mito and miscarraiges

>Date: Wed, 14 Feb 2001 17:20:49 EST

>

>In a message dated 2/9/2001 12:19:24 PM Eastern Standard Time,

>whyten@... writes:

>

>

> > I also have had 2 miscarriages, but am thought to be free of mito and am

> > relatively healthy. LOL

> > My oldest daughter (8yo) is healthy, followed by first miscarriage at 9

> > weeks, second miscarriage at 19 weeks(we did do chromosome studies this

> > time, came back totally normal 46 X,Y), then came Gracie, 3yo, (with

> > who knows what kind of something going on), and then 13 months later

> >

>

>Sorry a little late in responding to this thread. I also had 2

>miscarriages.

> My son Jake will be 8 in April and now undergoing extrensive work-up do

>the

>the fact that they think he may be mildly effected with the same mito

>disorder as Clayton. After Jake I got pregnant when he was 9 months old.

>I

>lost that baby at 26 weeks - due to a placental abruption - she was

>stillborn. I am told that she was healthy - or at least no chromosomal

>damage. After the fact I was found to have a high ANA and anticardio

>lipobodies (I think that is the name) and thus with my next pregnancy - the

>twins I was on heparin, baby aspirin and predisone. Well actually between

>the

>twins and Jake - and very early - before I started the regimn above - I

>lost

>one at 6 weeks. They do not know why. After that I carried the twins to

>34

>weeks - but very difficult pregnancy - and also they did see lots of

>problems

>with clayton throughout the whole pregnancy.

>

>Well Clayton was diagnosed with mito - complex I in April of 1999 and now

>we

>are having a work up on Jake. Clayton's twin Cole seems to be ok.

>

>Love,

>Sharon

_________________________________________________________________________

Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com.

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dr tick, the doctor who diagnosed my sister and me, did not say anything

about miscarriages and premature babies being related to miscariages.

But it is my own feeling that they are. They also run in my family with my

maternal grandmother having at least one we know of. My aunt we know had

one stillborn baby, my mother had one. I myself was also premature but i do

not know how early. My sister's first baby was born at 24 weeks or so,

lived one hour. Her second was born at 29 weeks. She also had a

miscarriage in between there. I was fortunate. My son was born a month

early because we decided to induce as there was not enough fluid around him

and i was diabetic.

If you are thin may have something to do with it also. Or, like someone

else said, if the mitochondria are very bad, it is the bodies way of not

bringing that baby into the world.

Re: mito and miscarraiges

> >Date: Wed, 14 Feb 2001 17:20:49 EST

> >

> >In a message dated 2/9/2001 12:19:24 PM Eastern Standard Time,

> >whyten@... writes:

> >

> >

> > > I also have had 2 miscarriages, but am thought to be free of mito and

am

> > > relatively healthy. LOL

> > > My oldest daughter (8yo) is healthy, followed by first miscarriage at

9

> > > weeks, second miscarriage at 19 weeks(we did do chromosome studies

this

> > > time, came back totally normal 46 X,Y), then came Gracie, 3yo, (with

> > > who knows what kind of something going on), and then 13 months later

> > >

> >

> >Sorry a little late in responding to this thread. I also had 2

> >miscarriages.

> > My son Jake will be 8 in April and now undergoing extrensive work-up do

> >the

> >the fact that they think he may be mildly effected with the same mito

> >disorder as Clayton. After Jake I got pregnant when he was 9 months old.

> >I

> >lost that baby at 26 weeks - due to a placental abruption - she was

> >stillborn. I am told that she was healthy - or at least no chromosomal

> >damage. After the fact I was found to have a high ANA and anticardio

> >lipobodies (I think that is the name) and thus with my next pregnancy -

the

> >twins I was on heparin, baby aspirin and predisone. Well actually between

> >the

> >twins and Jake - and very early - before I started the regimn above - I

> >lost

> >one at 6 weeks. They do not know why. After that I carried the twins to

> >34

> >weeks - but very difficult pregnancy - and also they did see lots of

> >problems

> >with clayton throughout the whole pregnancy.

> >

> >Well Clayton was diagnosed with mito - complex I in April of 1999 and now

> >we

> >are having a work up on Jake. Clayton's twin Cole seems to be ok.

> >

> >Love,

> >Sharon

>

> _________________________________________________________________________

> Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com.

>

>

>

>

> Brought to you by www.imdn.org - an on-line support group for those

affected by mitochondrial disease.

>

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Thanks to everyone thats commented on this possible connection...it

really has helped. My sister is going to be able to travel with me and

the kids to see Dr Cohen at the end of this month (10 days and counting)

so it will be interesting to see if he has any comments on it while we

are there. I promise to let you all know if he has anything to say

about it!!!!

I also wanted to offer my condolences for your losses. I have never

been through the pain of a miscarraige, so can only imagine how

difficult it is to get through, and talk about even a while after the

fact. So your willingness to share this with me has meant a great deal

to me and I am deeply appreciative of your openess here.

BIG hugs,

Kass, mom to Chance(7 1/2) and Madison(4)...both suspected mito, seeing

Dr. Cohen on the 26th, and Abby(3)

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