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         Down Syndrome:     more books (100)
  1. Down Syndrome Across the Life Span by Monica Cuskelly, Anne Jobling, et all 2005-12-05
  2. Biomedical Concerns in Persons With Down Syndrome by Siegfried M. Pueschel, 1992-07

141. MayoClinic.com - Down Syndrome
A description of the disease plus complications, risk factors, diagnosis and treatment.
http://www.mayoclinic.com/home?id=5.1.1.4.5

142. Down's Syndrome Screening
What are the screening methods for down s syndrome during pregnancy andhow can it be ruled out for definite? down s syndrome screening.
http://www.womens-health.co.uk/downs.htm
Down's syndrome screening
Down's syndrome (DS) is the commonest single cause of mental handicap in children of school age. It is caused by a change in one of the genes in the egg before it is fertilised by the sperm (at the time of conception). This is usually a completely random happening, though it is more common in older mothers. Throughout the world, the frequency of DS is about 3 per 2000 births.
Amniocentesis Down's syndrome can be diagnosed early in pregnancy (at about 15-16 weeks) by amniocentesis. This involves a very fine needle being passed into the womb, under guidance by ultrasound, and sampling of the (amniotic) fluid around the baby. It is done under local anaesthetic, and most women don't find it too uncomfortable. There is a risk, however, of about 1 in 100 to 200 of a spontaneous miscarriage after the procedure. Because of this miscarriage rate, amniocentesis is only offered to women deemed to be at high risk of having a baby with Down's syndrome. Similarly, it must be something that you have thought about at length, discussed with your partner and feel that you would opt for a termination of the pregnancy, were you found to be carrying a baby with DS. Clearly, if this is not something you would consider, then you most likely would not wish to risk miscarriage, just to know. It is also important to remember that people with Down's Syndrome can have long, fulfilling lives. There are a lot worse things that can happen.

143. GMDSA Home Page
Provides information on down's syndrome and support to parents, carers and professionals. Online newsletter, and list of resources.
http://members.aol.com/GMDSA/
GM DSA
Greater Manchester Branch of the
Down's Syndrome Association

Reg. Charity 1061474 email us
Welcome to The GMDSA Homepage
The Greater Manchester Branch of the Down's Syndrome Association, now has a presence on the World Wide Web. The GMDSA is a parent led support group to provide information for parents, carers and professionals on all matters concerning Down's syndrome. On our Web site you can:
What is the GMDSA?
We are a group of parents who live in the Greater Manchester area. Most of us care for a child or adult who has Down's syndrome. We provide information and advice through our courses, newsletter and library. Social events for the family are arranged so that families can meet one another. Committee members meet regularly and anyone is welcome to attend and lend a hand. We can arrange for new parents to be introduced to other parents for advice or just a listening ear. Who's who and who we are Visitors since 23th June 1998 Web Search Engines Google Last updated 8th June 2002

144. New Home Page
Offers support and information to families who have a member with down's syndrome and congenital heart defects. Forum and contact details.
http://www.downs-heart.downsnet.org/
DOWN'S
HEART
GROUP Information about heart defects related to Down's Syndrome UK Charity No 1011413
The Down's Heart Group is a UK charity which offers support and information to families who have a member with Down's Syndrome and congenital heart defects On this site you will find information about heart defects, tests and procedures, and other topics of interest, as well as details of the support and information available from the Down's Heart Group Everyone involved with the Group is themselves a parent (if not natural, then foster or adoptive), or in a few cases a grandparent. We have all found it helpful to be in contact with other families, perhaps it would help you too.
Contact Information
If you feel we may be able to help you or someone you know, please contact us. Telephone FAX Postal address 17 Cantilupe Close
Eaton Bray
Dunstable
Beds
United Kingdom Electronic mail Downs_Heart_Group@msn.com Mailing List You might like to subscribe to the Downs-Heart mailing list which is specifically for those interested in the heart problems associated with Down's Syndrome. Particularly useful for asking questions and sharing experiences with other families from all over the world.
To subscribe, click on the link below then follow the instructions.

145. The Young Downs Group
A support group for parents of young children with down's syndrome in Norwich. Meeting and contact details.
http://www.paston.co.uk/users/maygurney/dsa.html
The Young Down's Group For families, carers and friends of Young Children With Down's Syndrome.
A chance to share the difficulties and the joys,
information and ideas over a coffee.
Every Wednesday from
10 am to 12 noon
at
St. Anne's Church
Colman Road
Norwich
(Car Parking available) If you bring your children with you there will be plenty
of toys to play with. Brothers and sisters are most welcome If you would like more details or would like to come but have difficulty with transport please contact Email Wayne Doman Return to index page The Portsmouth Down's Syndrome Trust The Down's Syndrome Association ... For All the Special Kids in the World

146. CERI Down’s Syndrome Page
The down’s syndrome Page. Additional discussions of down’s syndrome havetaken place in the Question Answer section of Smart Drug News.
http://www.ceri.com/downhome.htm
Return to the Cognitive Enhancement Research Institute Home Page or Special Menus Page
The following two articles are reproduced here in their entirity, complete with graphics, charts, sidebars and scientific references. targetted nutritional intervention (TNI). Starting with the pioneering work of Dr. Henry Turkel and leading up to the latest contributions of Dixie Lawrence, this article lays a foundation for the articles to follow. It is reproduced here in its entirity. An Interview with Dixie Lawrence: This full-length interview with Dixie Lawrence detailed many of the approaches Dixie pioneered with her daughter and provides many practical tips for the successful implementation of nutritional therapy and piracetam in children. It is reproduced here in its entirity. The following three articles are presented only in part. Introductory paragraphs are presented in full-text, and the rest of the articles are summarized. References are omitted. This article focusses on nutrition issues surrounding collagen (connective tissue) metabolism, methylation metabolism, ammonia metabolism and mineral deficiencies. i.e.

147. Dsa-northeast.org.uk
Branch of the down's syndrome Association offers parental counselling, subsidised leisure activities, Christmas parties and events, playgroups, and newsletters to people with down's syndrome, their families and their carers.
http://www.dsa-northeast.org.uk/
The website for dsa-northeast.org.uk can be found by clicking here . dsa-northeast.org.uk is registered through Easily.co.uk - get web site hosting or domain name registration here

148. Ups And Downs
A support group of parents of children with down's syndrome in Southampton. Information about activities and resources, with contact details.
http://mysite.freeserve.com/UpsandDowns/

149. PODS (Parents Of Down's Syndrome)
Provides support, friendship and information for parents and carers of children with down's syndrome in Barnet and surrounding areas. Information on activities, stories, and contact details.
http://www.pods.org.uk/

150. The Young Downs Group
A support group for parents of young children with down's syndrome in Norwich. Meeting and contact details.
http://www.pastonroot.co.uk/maygurney/dsa.html
The Young Down's Group For families, carers and friends of Young Children With Down's Syndrome.
A chance to share the difficulties and the joys,
information and ideas over a coffee.
Every Wednesday from
10 am to 12 noon
at
St. Anne's Church
Colman Road
Norwich
(Car Parking available) If you bring your children with you there will be plenty
of toys to play with. Brothers and sisters are most welcome If you would like more details or would like to come but have difficulty with transport please contact Email Wayne Doman Return to index page The Portsmouth Down's Syndrome Trust The Down's Syndrome Association ... For All the Special Kids in the World

151. Untitled Document
Collaboration between the down's syndrome Association and St George's Hospital Medical School, University of London, has produced a comprehensive information resource, with particular emphasis on the ability of medical professions to empower their patients.
http://www.intellectualdisability.info/

152. Initiative For People With Down's Syndrome
Includes photos of children from around the world, and an online exhibition entitled Variety Enriches Our World.
http://members.aol.com/InitiativeDown/index.htm
Exhibition Gallery UPPS
Initiative for people with
Down's Syndrome
Ultrasound picture of a child with Down's syndrome in the .week of pregnancy Initiative for people with Down's Syndrome Dr. med. Bernhard Möller und Isabella Möller Kiefernweg 26D - 33014 Bad Driburg Germany to the german version of this site I n December 1998 founded association in Germany, which wants to inform the public about and support people with Down's syndrome. D own's syndrome is no disease, but a variant of the human chromsomes with the chromosome 21 present in each cell three times (instead of otherwise twice). It is usually not hereditary, but emerged by chance. Children with Down´s syndrome show a slower development, which extent is individually different. No one knows, which possibilities of development exist with appropriate help. W e would like to encourage affected parents, to accept their child as it is, in order to say"Yes". We fight for these right to live and will never let the human dignity of our sons and daughters be undermind. We think it is not acceptable, that today in 98 % pregnancy is interrupted after prenatal diagnosis of down's syndrome.You must remember, that according to the law in Germany an abortion is possible from medical indication until the moment of birth.

153. Camp Jened - Rock Hill, NY
Provides a vacation for adults who have a wide range of physical and developmental disabilities, such as Cerebral Palsy, Downs syndrome, Autism and Behavior Disorders. Located in New York.
http://www.campjened.org/

Camp Jened
Serving adults with disabilities Are You Ready For Some Magic?
Who Does Camp Jened Serve?

Staff Information

Staff Application

Contact Us
...
Camp Jened Mailbox

154. The EASe "Electronic Auditory Stimulation Effect" CD For Auditory Hypersensitivi
For auditory hypersensitive, autistic, downs syndrome, pdd and add children.
http://www.vision-audio.com/visiondocs/ease.htm

155. Living With Asperger's Syndrome
One family's story of the ups and downs when one of its members is affected by Asperger's syndrome.
http://www.mumof4.pwp.blueyonder.co.uk
living with asperger's syndrome A family's story with links for information on autism, asperger's syndrome and support sites. Please click above to enter This site is a member of WebRing. To browse visit here

156. BADSS - Bristol Area Downs Syndrome Support
A parentled support group for the parents and carers of those with Downs syndrome.
http://www.dsa-bristol.org.uk/
BADSS - Bristol Area Downs Syndrome Support Click here to enter site To contact BADSS, email info@dsa-bristol.org.uk or telephone 0117 9652974

157. Wonderland Camp For The Physically And Mentally Disabled
Missouri camp provides summer programs for adults and children with physical or mental challenges including MS, multiple dystrophy, cerebral palsy, downs syndrome, praderwilli syndrome.
http://www.wonderlandcamp.org/
    Welcome to Wonderland Camp
A Special Camp for Special Friends
On the Lake of the Ozarks
W
onderland Camp is dedicated to serving mentally and physically challenged individuals of all ages for over 30 years. Great News
The Missouri Jaycees
Mid Missouri Mavericks
Night at the Ball Park!
It will be on Friday, August 13, 2004 7pm at the University Campus Taylor Stadium. Tickets are $4.00 and Wonderland Camp will receive 1/2 of every ticket sold!!
For tickets please contact Jackie Bax at 573-897-9937, baxj@lincoln.edu (work), bax60590@midamerica.net (home)
or you can call Gerry Moore at 314-591-2960 (cell) 636-397-6391 (home), Gmmotgrs@aol.com
Don't forget you can always call Wonderland Camp at 573-392-1000.
Hope to see you there!! About Us
Wonderland Camp is the dream of Charles J. Miller. He worked with the Missouri Jaycees to build a residential summer camp for the mentally and physically challenged children and adults. Today Wonderland is a place where they can enjoy the exhilaration of outdoor living and play together for one magical week. Click here to learn more about Wonderland Camp Camping Programs
We offer summer camp programs from the end of May through August. Campers can enjoy the beauty of the outdoors, develop friendships, and participate in special events. Click here to learn more about our

158. A Parents Resource

http://www3.sympatico.ca/terry.edwards/Shelby.html
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159. DSA Information
hyperlink to index hyperlink to index.
http://www.dpa.org.sg/DSA/

160. Online Shopping
Translate this page Online Shopping ENTER Special links Hotel. Online Shop. Kleinanzeigen.Shopping. Hotel intern. Servicerufnummern. CDs. Warenproben.
http://dsapenang.freeservers.com/

Online Shopping

ENTER

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