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location not given

Affected Person: Aug 2007 
Family type:
Siblings: 1
Disabled siblings: 0

Username: adamalex0508
Relationship: Mother

Other conditions: None

Last updated: 29 Nov 2007

Brief summary: I was 21 when I gave birth to my perfect son. My husband and I decided to try again and found we were pregnant with #2. I was 22. After some slight bleeding, I went in for my first ultrasound. It was found that the baby had died. After going for a D&C, it

Worcestershire ( West Midlands )

Affected Person: Jan 2008 
Family type:
Siblings: 1
Disabled siblings: 0

Username: BILLY44
Relationship: Mother

Other conditions: None

Last updated: 18 Aug 2008

Brief summary: I FOUND OUT THAT MY BABY HAD TRIPLODY AT 36 WEEKS AND WE DECIDED TO END THE PREGRENCY, WAS POORLY ALL THE WAY THROUGH BUT NO ONE MEDICAL WISE COULD FIND ANYTHINK WRONG BUT DEEP DOWN I NEW IT DIDNT FEEL RIGHT ! EVENTUALLY I WAS GIVEN A CVS TEST AND AMIO WH

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Condition (also listed as)	No. of members	Support Group
Chromosome 1 Disorder	10
Chromosome 10 Disorder	5
Chromosome 11 Disorder	1
Chromosome 12 Disorder	14
Chromosome 13 Disorder	1
Chromosome 15 Disorder	9
Chromosome 16 Disorder	0
Chromosome 17 Disorder	14
Chromosome 19 Disorder	1
Chromosome 2 Disorder	4
Chromosome 20 Disorder	3
Chromosome 21 Disorder	3
Chromosome 22 Disorder	3
Chromosome 3 Disorder	3
Chromosome 4 Disorder	4
Chromosome 5 Disorder	5
Chromosome 6 Disorder	5
Chromosome 7 Disorder	2
Chromosome 8 Disorder (Chromosome Disorders, Tetrasomy 8p)	9
Chromosome 9 Disorder	3
Chromosome Marker	0	-
Chromosome X Inversion syndrome	0	-
de Grouchy Syndrome I (18p- syndrome; 18p deletion syndrome; chromosome 18p monosomy; del(18p) syndrome; deletion 18p syndrome; monosomy 18p; partial monosomy 18p )	4	-
De Grouchy Syndrome II (18q- syndrome; 18q deletion syndrome; chromosome 18q; del(18q) syndrome; deletion 18q syndrome; monosomy 18q; partial monosomy 18q )	9	-
De La Chappelle syndrome (XX Male syndrome)	0	-
isodicentric 15 (idic(15))	10	-
L1 Syndrome (L1 Spectrum; L1 Disease; CRASH syndrome. Includes: HSAS; MASA syndrome; SPG1 (X-linked complicated hereditary spastic paraplegia type 1); X-linked complicated corpus callosum agenesis.)	1	-
Monosomy 1p36 deletion syndrome	28	-
Mosaic Variegated Aneuploidy	0	-
Penta X Syndrome (XXXXX Syndrome)	0	-
Ring Chromosome 18	0	-
Ring G Monosomy	1	-
Ring X	0	-
Translocations	5	-
Trisomy 14 Mosaic (Trisomy 14,Mosaic Trisomy 14,Trisomy 14 Mosaicism Syndrome)	0	-
Uniparental Disomy	0	-
XYY Syndrome (Jacob's Syndrome)	13