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Club Foot

10 people found, showing 1 to 10

To save room on the page we use the term disabled to indicate those with disabilities, special need or a medical condition.

 

Bedford Borough ( East of England Region )

Jul 2006  male
Family type: two parent family
Siblings: 1
Disabled siblings: 0
Username: Lewman
Relationship: Mother
Last updated: 16 Aug 2009
Brief summary: My little trouble maker has clubfoot, XYY syndrome and is very hypermobile. Also delayed speech and terrible temper tantrums can switch between happy and screaming mad at the blink of an eye!!!

Lincolnshire ( East Midlands )

Feb 2011  male
Family type: two parent family
Siblings: 0
Disabled siblings: 0
Username: scunny_titch
Relationship: Mother
Last updated: 19 Sep 2011
Brief summary: I'm 22, married and have one child, Lucas. He has XXYY syndrome, which is a genetic disorder, along with a couple of other hiccups which were picked up as soon as he was born.

location not given

Aug 1976  not given
Family type: not given
Siblings: 1
Disabled siblings: 0
Username: rabbit25
Relationship: Female Affected Adult
Other conditions:
Larsen syndrome (14)

Last updated: 10 Jan 2006
Brief summary: I have a Clubfoot aswell as Larsen's Syndrome.

London Boroughs ( England )

Jun 2012  female
Family type: two parent family
Siblings: 0
Disabled siblings: 0
Username: CatsMummy
Relationship: Mother
Last updated: 15 Jan 2016
Brief summary: Child with several health conditions including: Congenital Talipes (clubfoot); multiple allergies; sleep disorders; respiratory problems; immune deficiency and anxiety disorder. Two parent home but currently without any additional support.

Northamptonshire ( East Midlands )

Jul 2004  male
Family type: two parent family
Siblings: 0
Disabled siblings: 0
Username: Rachit
Relationship: Mother
Last updated: 14 Feb 2005
Brief summary: Both my son and my partner have Beals syndrome.

Renfrewshire ( Scotland )

Feb 2006  male
Family type: two parent family
Siblings: 2
Disabled siblings: 0
Username: elliebell
Relationship: Mother
Other conditions: None

Last updated: 08 Dec 2008
Brief summary: my name is carol iam 43 my son is ross who is nearly 3 he has a chromosome defect called 18q which causes him to have a lot of problems low muscle tone delayed development he has kidney reflux and is parcially sighted

South Tyneside ( Tyne and Wear )

Feb 2014  female
Family type: two parent family
Siblings: 2
Disabled siblings: 0
Username: mckenzie14
Relationship: Mother
Last updated: 01 Apr 2014
Brief summary: Hannah was born 10th Feb 14. She has been diagnosed with myleo Spina Bififa, Hydrocephalaus, Charii maliformation, Bilatired clubbed feet.syringomyelia and reflux.

Staffordshire ( West Midlands )

Aug 2008  male
Family type: two parent family
Siblings: 0
Disabled siblings: 1
Username: darek4
Relationship: Mother
Other conditions: Talipes (31)

Last updated: 06 Nov 2012
Brief summary: my son born with talipes, he after 4 operation on foot for now, he have problem with speach and behaviore.

United States of America ( Americas )

Jun 2011  male
Family type: two parent family
Siblings: 1
Disabled siblings: 0
Username: earthhe
Relationship: Female Family Member
Last updated: 14 May 2012
Brief summary: my nephew is nearly 1 and has: thin corpus callosum, nystagmus, hypotonia, an arachnoid cyst, high myopia, one club foot, microcephaly, and possible ventriculomegaly and micrognathia.

Nov 2013  female
Family type: two parent family
Siblings: 0
Disabled siblings: 1
Username: undefined1
Relationship: Mother
Last updated: 18 Feb 2016
Brief summary: My daughter has VACTERL association (VATERS) for her it includes: solitary kidney, tethered spinal cord,imperforated anus, double hip dysplasia, club foot, nurogenic bladder, and grade 5 bladder reflux, SUA, butterfly vertebra, and VSD.

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Related conditions 

There are conditions similar or related to this one that have people listed against them. They are listed below. If there are UK Support groups available, they will be indicated by this G icon. Click this icon to view the list of available support groups.

Condition (also listed as) No. of members Support Group
Congenital Vertical Talus 1 -
Dysplasia Epiphyseal Punctata (Epiphyseal Punctata) 0 -
Femoral Hypoplasia-Unusual Facies syndrome 31 -
Fibula Deficiency 0 -
Fibula Hemimelia 2 -
Idiopathic Chondrolysis of the Hip (ICH) 0 -
Kohler's disease 0 -
Larsen-Johansen syndrome 0 -
Lumbo-Sacral Plexopathy 0 -
Osgood Schlatter syndrome 0 -
Osteochondritis of the Upper Femoral Epiphysis 0 -
Perthes disease (Larsen-Johansson syndrome; Osteochondritis of the Upper Femoral Epiphysis; Epiphyseal Dysplasia) 47 G
Pes Cavus 0 -
Proximal Femoral-Focal Deficiency 21 -
Severs disease 4 -
Slipped Epyphysis 1 -
Talipes 31 -
Tibial Hemimelia (Congenital Longitudinal Deficiency of the Tibia) 2 -

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