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Coats' Disease

also listed as Exudative Retinitis

8 people found, showing 1 to 8

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

 

Cheshire East ( North West )

Jan 1953  male
Family type: not given
Siblings: 1
Disabled siblings: 0
Username: ollytheblue
Relationship: Male - Same Person
Other conditions: None

Last updated: 12 Apr 2008
Brief summary: Lost my left eye in 1956 to coats disease.

England

Mar 2006  female
Family type: two parent family
Siblings: 0
Disabled siblings: 0
Username: pochiluv
Relationship: Mother
Last updated: 14 Jul 2010
Brief summary: not given

Essex ( East of England Region )

Oct 1992  female
Family type: two parent family
Siblings: 2
Disabled siblings: 0
Username: Huffy92
Relationship: Female - Same Person
Other conditions: None

Last updated: 20 Feb 2009
Brief summary: add me on facebook Skye Hough

Palestine ( Middle East )

Feb 1989  female
Family type: two parent family
Siblings: 8
Disabled siblings: 4
Username: Abu Hatem
Relationship: Female Friend
Other conditions: None

Last updated: 13 Jul 2007
Brief summary: I am working as a consultant on health projects and through my work, I came across this female case who was diagnosed as Coats' disease. The parents of this case are from a very simple family living in a village around Hebron city in the West Bank. T

Royal County of Berkshire ( South East )

Nov 2003  male
Family type: two parent family
Siblings: 1
Disabled siblings: 0
Username: maddijp
Relationship: Mother
Other conditions: None

Last updated: 06 Feb 2009
Brief summary: My son is 5 years old and has been diagnosed with Coats' Disease. You can find and add me on Facebook under Maddi Pitfield. Please contact me on there. Thank you.

Jul 2005  male
Family type: two parent family
Siblings: 2
Disabled siblings: 1
Username: tandberg
Relationship: Father
Other conditions: None

Last updated: 19 Sep 2008
Brief summary: Male, 3 years old, normal, happy, loves life. Diagnosed with Coats disease in the left eye in September 2008.

Stirling ( Scotland )

Jun 1996  male
Family type: two parent family
Siblings: 2
Disabled siblings: 0
Username: scattiemare
Relationship: Mother
Last updated: 08 Aug 2008
Brief summary: My son had his right eye removed in 1999 at the age of 3 due to Coats Disease. He has for years displayed signs of trauma and has struggled to come to terms with having an artificial eye.

Surrey ( South East )

Jul 2003  male
Family type: two parent family
Siblings: 1
Disabled siblings: 0
Username: MONIQUE
Relationship: Mother
Other conditions: None

Last updated: 16 Nov 2006
Brief summary: We are a family of 4 who live in Surrey. In July, we were told that our son has Coats disease. He is blind in his right eye. Coats is a very rare condition and no support group currently exists.

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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 -
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
Homonymous Hemianopia 6 -
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 5 -
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) 10 -
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 0 -
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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