Tuesday, February 21, 2012

REGISTERED CARE MANAGER - Deafblind Charity

[Article Ad for position for working with deafblind people from he Guardian in the UK. ~K]

REGISTERED CARE MANAGER - Deafblind Charity: Are you a Deputy or a Registered Care Manager looking to
develop a specialism in working with deafblind people? Our client is a national charity providing support and advice to people who are deafblind, their families, friends and professionals.

How I’m Coming to Terms With the Genetic Condition I May Have Passed to My Son

efore having children, the farthest I thought about genetics was assumptions on whose eye color my children would have or whether they would get my nose, or my husbands hands. I thought of the word “hereditary” in relation to characteristics, not in regards to diseases, illnesses and conditions.
But a quick google search after Arlo’s diagnosis of Ocular Albinism at 3 months old led me to the words “x-linked hereditary” — meaning it is most commonly passed from mother to son. I felt a knot forming in my throat as I read that the gene can be passed from generation to generation before it presents itself in a member of a family. It also meant that if I carried the OA gene, there was a 50% chance that any son we had would also have the condition.
I gave him this, I thought my eyes burning with tears. I felt dirty, betrayed by my genetic makeup, angry that this wonky gene had layed quietly inside me and now I had passed it to my son. I was ashamed of it, mostly because I didn’t understand albinism yet. I was so fearful of the unknown.
Six months since his initial diagnosis, my mindset around albinism has changed drastically. I’ve discovered that first and foremost, albinism is nothing to fear. As far as chromosomal abnormalities go, it’s a pretty mild one. It doesn’t effect his life span, his bodily functions (save for his vision to some extent, bit there are a lot of resources to help him there) and it does not cause him pain. Arlo is also fortunate in that he does have some pigmentation, so most people are not even aware that he has it.


[For the rest of the story follow this source link: http://blogs.babble.com/babys-first-year-blog/2012/02/21/how-im-coming-to-terms-with-the-genetic-condition-i-may-have-passed-to-my-son/]

Amblyopia and Strabusmus

My two month-old baby’s eyes don’t seem to work together. Since I had a “lazy eye,” do you think my son will too?
There are several different medical conditions that may be referred to by the lay population as lazy eye. The two major types are Amblyopia and Strabismus.
For the nine months that the child was developing inside the uterus there was no need for the eyes to focus on a single point with both eyes. Once the child is delivered he/she needs to learn how to focus on a subject in front of him/her. Initially the eyes see independently. This of course could be very confusing to the brain to process these separate images and understand it’s environment. Thus over the first four months of life, the child develops this ability to focus with both eyes thereby developing binocular vision (3-D vision with depth perception). If there is any obstruction to clear vision (such as a cataract), if the eye can’t focus, or if there is another condition not correctable by eyeglasses, Amblyopia will develop. Since it is too difficult to make sense of the unfocused and focused views, the brain “shuts down” the blurred vision. Thus, if there is no intervention made, the child’s vision will worsen in the eye that started with the problem. This condition is estimated to occur in approximately 3 percent of children. Most of these types of problems are random conditions, and do not seem to “run in families.”
Chidren with a Strabismus are unable to align their eyes for proper vision due to a weakness or descepancy in the length of one of the muscles of the eye; therefore, when the eyes try to focus, they cannot do so for more than a short time, and the eye will stray. This causes two separate images, and the child may see “double” because of it. Once again, since this is difficult for the brain to proces, it will frequently “shut down” one of the eye’s images thereby reducing the acuity of that eye. This then leads to Amblyopia or a true “lazy eye.” The incidence of this condition is approximately 5 percent of children. There is a tendency to see this trait in families without a true genetic inheritance. If one parent had a “lazy eye” in their past, then there is a somewhat greater degree of one their offspring to have one; however, it is not that much greater than the general population.
Children prior to four months will have eyes that seem to “wander.” After this time they should remain straight and focused. If there are any concerns, it is necessary to make sure that your child is evaluated.
Good Luck
DRTOM

Friday, February 17, 2012

Young golfer doesn't accept blindness as handicap

Young golfer doesn't accept blindness as handicap

Underage Drinking Video Contest for Teens

MADD National is sponsoring a teen video contest, and the prizes are awesome - like iPads and trips to D.C.  The link below explains it all.