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louise - Jorja's Mommy
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« Reply #30 on: January 02, 2008, 05:14:39 PM » |
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 Emma, I am so sorry to have to welcome you ourforeverbabies, and i am so sorry for the loss of Daniel. Sadly we have quite a lot of Mommies on here who have lost babies to SIDS. I look forward to getting to know you better and hearing all about Daniel when you are ready. Take Care Louise x 
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MammytoAbigail
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« Reply #31 on: January 30, 2008, 09:34:44 PM » |
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hello, ive been on here for a while but didnt no where me and Abigail 'fit' so to speak.... ive desided that we belong here hehe.............Im Lucy im 20 years old i gave birth to my beautiful Princess in December 30th 2006!...at 36weeks and everything seemed a bit het up!! Abigail was rushed to neonatel unit with breathing difficulties she was born at 4lb 14oz soooo they put it down to size.... on the 1st January 2007 they found out Abigail had a heart defect.... cutting along story short which you can read on gonetoosoon please feel free....we later found out she had no immune system and that she had CHARGE syndrome.. Abigails heart couldnt take much more and flew to heaven at 20 weeks on May 24th... im now pregnant again with Olivia, Abigails sister whom is due May 25th 2008 (very close to Abigails angel date) thank you for reading i hope i get to no you all better very soon xxx
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macysmummyKat
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« Reply #32 on: March 15, 2008, 08:10:10 PM » |
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Hiya im Kat im 28 and lost my daughter macy aged 22 months to renal failure on the 4th march
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donna64p
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« Reply #33 on: April 02, 2008, 09:33:55 AM » |
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hi my name is donna im new so dont now realy what to do . i lost my son lee in 1986 it was a cot death he was 18 weeks old they say time is a good healer but it asnt worked for me i seem to miss him more now then i did all i wish is that i could just hold him and let him now that i am there and that i love him so much
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amyclarks mummy
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« Reply #34 on: May 09, 2008, 12:12:28 AM » |
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 it's a great community to share your feelings with and i have found it does help to get it all off your chest.
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vicki73
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« Reply #35 on: March 08, 2009, 09:13:41 PM » |
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Hi, Not sure where Freya and I fit because even though she was in the NICU all of her short life she was 10 weeks old when she died so thats not strictly neonatal. Anyway, Im Vicki and my husband Steve and I lost our precious little girl Freya in April 2007. We found out after her death that she had a rare genetic disorder called complex 1. She was born at 27 weeks and was a real little fighter but sadly there was nothing more the hospital could do for her in the end.....god knows they tried. I miss her every day and have a Freya shaped hole in my heart which will remain until I meet my beautiful girl again. x 
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Teresa ~ Keaton's Mommy
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« Reply #36 on: March 09, 2009, 09:01:23 PM » |
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 Hi Everyone My name is Teresa and I am 34 years old. Keaton was my middle of three children and my only son. He was born on 28th Feb 2005 and was taken by SIDS on 15th April 2005 aged 6 weeks and four days. Keaton has a big sister who is 8 and a baby sister who is 9 months old. As with so many SIDS babies Keaton was perfectly healthy and perfectly developed his PM showed that there was no reason why our little man should of died.  love to you all and all our little angels  xxx
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kimbobt84-BensMummy
OFB Support Team
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My Little Man Ben 10/05/07-04/06/07
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« Reply #37 on: March 09, 2009, 11:40:44 PM » |
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don't think i ever filled this in. Well, ben was only 3 weeks old when he died but to me he was past neonatel as he came home and lived his short life as we knew he was dying. My names kim, i'm 25, and live in castleford, near leeds/wakefield, west yorkshire. I live with my fiance of 8yrs lee and we have been blessed with 4 gorgeous children ashleigh 5, lucy 2 and the twins ben and holly 1. I'll tell you a short version of my gorgeous little mans life but also feel free to read his story on gts, ben warburton. I carried the twins to 37wks and we wernt aware of any problems. Ben was born with a rare syndrome called Golden Har, at the severe end of the scale, ben had facial deformities which meant he was blind and deaf. He had a serious heart defect but we decided not to operate due to finding out ben was severly brain damaged. Ben couldnt move, his spine was fused, blind, deaf, would suffer fits/epilepsy, cleft palette, the mind of a 3mth old maximum, god the list is endless for what my poor boy had. We brought him home, lived as a family for 12 special days and cuddled him as he passed away peacefully in our arms, just us, at home. We miss him so much but if taking bens pain away meant living with the pain myself id do it time and time again. Bens sisters keep me going, they are all healthy.
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Gerry
Full Member
 
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Hi my name is Donna and i am Gerry's mom
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« Reply #38 on: May 09, 2009, 02:48:14 PM » |
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Please introduce yourself here and share whatever details you are comfortable with.
Hello my name is Donna. Five weeks ago our beautiful baby Gerry passed away during the night. He was 9weeks and 2 days old. The day before he died he celebrated his baptism. The postmorten didn't find anything so at the moment we are assuming it was SIDS. Do you think it is right for us to try for another baby.
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Olliemam+1
My Precious Angel
OFB Support Team
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xxxxx.
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« Reply #39 on: May 09, 2009, 05:09:50 PM » |
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Hello Donna I am so sorry for your loss, how beautiful is your Gerry xxxxx. Tyring again is such a personal thing, all I can say is that you and your partner try again when you are ready. Looking forward to getting to know you and Gerry better when you are ready. Take care Dawn xxxxx. 
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gemmab82
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« Reply #40 on: November 21, 2009, 07:49:49 PM » |
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Hi my names gemma im new to the site i lost my daughter elisha to s.i.d.s in june 2000 she was 4 months old. I was 17 at the time of her death and still blame myself. Thanx for listening xx 
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