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Homonymous Hemianopia

6 people found, showing 1 to 6

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

 

Devon ( South West )

Dec 2005  female
Family type: two parent family
Siblings: 3
Disabled siblings: 0
Username: FREYASMUM
Relationship: Parent
Last updated: 04 Sep 2008
Brief summary: Our very lively little girl has lots of health problems. She is hypothyroid, has no left field of vision, hearing difficulties, failure to thrive, hypermobile, anterior placed anus, developmental delay, some dysmorphic features (a little bit elf like- ver

Hertfordshire ( East of England Region )

Jun 2001  female
Family type: two parent family
Siblings: 2
Disabled siblings: 1
Username: scampie
Relationship: Mother
Last updated: 16 May 2008
Brief summary: My daughter Mia was born with hydrocephelus caused by bleed before she was born. She has 2 VP shunts, hemiplegia, and severe visual impairment. She has more recently developed epilepsy.

Kensington and Chelsea ( London Boroughs )

Dec 1999  male
Family type: single parent family
Siblings: 2
Disabled siblings: 0
Username: Wonder
Relationship: Mother
Last updated: 09 Mar 2006
Brief summary: My son has quadraplegic cerebral palsy, left field homonymus hemianopia, mild nystagmus, (registered partially sighted),arrested hydrocephalus and global deveopmental delay. Where to go to play/meet people

Kent ( South East )

Jul 1997  male
Family type: single parent family
Siblings: 2
Disabled siblings: 0
Username: lilmannmum
Relationship: Mother
Last updated: 23 Jan 2010
Brief summary: my son had a massive brain haemorhage in 2007, he was 9... it left him with permanent brain damage

location not given

May 2005  male
Family type: two parent family
Siblings: 2
Disabled siblings: 0
Username: huxleycastle
Relationship: Mother
Other conditions: Hydrocephalus (87)

Last updated: 20 Mar 2006
Brief summary: My son was born with hydrocephalus after 2 brain haemorrhages pre natal and has left haemianopia. He has a sister and brother.

Somerset ( South West )

Oct 2005  female
Family type: two parent family
Siblings: 0
Disabled siblings: 0
Username: clockhouse
Relationship: Mother
Other conditions: None

Last updated: 11 Dec 2006
Brief summary: right hemonymous hemianopia

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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
3rd Nerve Palsy of the Eye 2 -
Achromatopsia 0 -
Acute Zonal Occult Outer Retinopathy (AZOOR) 0 -
Adie Syndrome (Holmes-Adie Syndrome) 2 -
Ametropia 0 -
Aniridia (Congenital Abnormality of the Iris) 13 -
Anophthalmia (Heminasal Aplasia) 4 G
Axenfeld Syndrome (Axenfeld Anomaly; Axenfeld-Rieger Syndrome; Rieger Syndrome) 0 -
Axenfeld-Schürenberg Syndrome (Cyclic Oculomotor Paralysis; Congenital Cyclic Oculomotor Paralysis) 0 -
Cataracts 20 G
Choroideremia 0 -
Chromotosia Congenita 0 -
Coats' Disease (Exudative Retinitis) 8 -
Coloboma 13 -
Colourblindness 0 -
Cone Dystrophy (Combined Cone-Rod Degeneration; Progressive Cone-Rod Degeneration; Cone-Rod Dystrophy; Retinal Cone Degeneration; Retinal Cone Dystrophy; Retinal Cone-Rod Dystrophy) 1 -
Congenital Stationary Night Blindness 6 -
Corneal Dystrophy 5 -
Eales Disease 1 -
Familial exudative vitreoretinopathy (FEVR) 2 -
Glaucoma 10 G
Idiopathic Optic Atrophy 1 -
Keratoconus 2 G
Macular Disease 0 G
Macular Dystrophy 1 -
Microphthalmia 5 -
Nystagmus (Spasmus nutans,Congenital Idiopathic Nystagmus) 21 G
Nystagmus and Astigmatism 7 -
Ocular Disorders (Drusen Syndrome) 0 -
Optic Nerve Atrophy 6 -
Optic Nerve Dysplasia 2 -
Optic Nerve Hypoplasia 20 -
Persistant Hyperplastic Primary Vitreous 2 -
Peter's Anomaly 7 -
Peter's Plus Syndrome (Peter's Plus Anomaly) 11 -
Pigment Epithelium retinal detachment 0 -
Post Polymorhous Corneal Dystrophy 0 -
Reis-Büclers (Reis-Bncklers) 0 -
Retinitis Pigmentosa (Bulls Eye Dystrophy; Central Areola Choroidal Dystrophy; Retinal Dystrophy, Tapeto Retinal Degenaration) 2 G
Retinopathy of Prematurity 1 -
Rieger's Anomaly 1 -
Rod Monochromatisim 0 -
Sclerocornea 3 -
Spheromicrophakia 0 -
Thyroid Eye Disease (Thyroid Ophthalmopathy; Thyroid Associated Ophthalmopathy; Graves' Eye Disease; Graves' Ophthalmopathy ) 1 G
Uveitis 1 G

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