Police in Los Angeles are appealing for public help in finding the sister of actress television aasha Davis, said the woman had disappeared six weeks ago after an argument with her husband.
Detective Chris Gable a press conference said that 46 years, Lesley Herring has not seen since February 8, and her husband, Lyle herring, not fully with the authorities.
Davis has had recurring roles in "Friday Night Lights" and "South of Nowhere".
Lesley herring, 44, was reportedly last visit, February 8 by her husband, Lyle, police in Los Angeles. She noted that the absence of his sister after discovering that his brother does not show up at work for several days.
At a press conference outside the lack of housing in 2700 Ms. Cahuenga Boulevard East, LAPD Detective Chris Gable indicated that the man is not his wife disappeared.
"I would be working as its fragmented and no less useful (a little) I wait for a man in mourning," said Gable.
But the detective, that humans are not considered suspects at this time.
"I know that no matter how crazy it seems. We study everything before I went to the Rush," said Gable. "It looks suspicious, and it seems, but I'm not on him (man), a suspicion confirmed, until I asked."
Lyle Herring also talked to reporters.
"If it's outside Lesley heard, please call us. Come to the house. Let us know what he said." I know we have much to discuss with the family, mother, your father, your brother and sister. "
In response to a direct question from a journalist KCAL9, if in any way responsible for the disappearance of his wife, herring replied: "No!"
Channel 9 Herring also said that his sister in law reported his wife missing, he also Rosarito Beach in Mexico in search of him. According to the couple took a leave for Valentine this place.
Gable told journalists that the man had appeared on 14 February, by cutting off his dreadlocks. He also said Lyle Herring was threatened, and with men of money, but not control, except to say that this was a guided tour.
[...]
Thursday, March 26, 2009
Sunday, March 22, 2009
Rebecca Alexander lose both visually and hearing impaired
This is the main story I never said. It is also the hardest. My sister, Rebecca, is wise, nature and really hysterically funny, the impressive and remarkable woman I've ever taken. She works as a psychotherapist and practitioner towers coming Spin she teaches 15 classes per week. It has it all, despite a disability, take away their vision and his hearing at a time.
Stop for a second opinion on that! The doctors told my sister, she is likely to go totally blind and deaf in the next 10 years. Since my sister he says, "It is, as I am slowly on the world around me, that the end of an old cartoon from the Warner Brothers television where the image is more smaller holes, and they fall and fades to black. "
Rebecca, 30, is a rare genetic disorder called Usher syndrome type III. It is among the most cruel of progressive disease of the normal flight of nearly 16,000 people in France. And currently, there is no treatment or cure. Rebecca bravely every day life with the hope that a treatment is found, before it is too late. My family and many others are determined by our commitment with the following organizations.
An extraordinary research effort is already under way by "Usher-III of the" Vision for the hope that if a team focuses on Rebecca error. I recently spoke with Dr. David Saperstein , Scientific Director of Usher III initiative, which said that its researchers are working on a multidimensional approach to slow or stop disease progression, including the development of specific drugs and gene therapy.
In addition, the fight against blindness of the Research Foundation of a wide range of retinal degenerative diseases, including Usher syndrome, and was the first important work helped to characterize the gene for Usher syndrome Type III.
There is no time passing, where I did not recall or put into question my loss of sight or hear, but it's my life and what are the cards I was dealt. I am not frightened by the progression of my condition, but I am concerned about the things I can not hear or see.
I have the same hopes and dreams like everyone else completely secure in person and consultation and my dreams are not weakened by the gradual loss of my visually impaired and deaf, but my disability was stronger and ready for all day. When I started losing my hearing, I learned the language and have a sense of belonging to the community of deaf and hearing impaired. When I started to deal with the idea of being blind, I was looking for a specialist mobility I learned how to be with a cane, if the time I needed, I would be prepared. I do not have time, and think of all sorts of things that can happen to me. I do not have time.
I always have on my life, whatever. So it'sa challenge to get help from others. However, as my visual and hearing are again in hindsight, I always easy to ask for help. Indeed, it was very liberating. It really helped me a connection with others, and others more comfortable and open with me about their own lives. I'm incredibly lucky, have a wonderful, loving and very loyal to family, friends. More I came to myself and my own face challenges, most are your relations with others to have. What I learned is that we can not live life on our own. We all need each other to help as many different ways.
Unfortunately, many of my greatest fears have been realized. I refused, my people, if discovered about my disability. I was alone in a very strong and dark bar people who do not understand that I needed to make your stay on my side. I even take a taxi. You name it, it's likely happened to me! But I can not live my life, because I face obstacles every day. My disability has a passion and energy to live my life fully. [...]
Stop for a second opinion on that! The doctors told my sister, she is likely to go totally blind and deaf in the next 10 years. Since my sister he says, "It is, as I am slowly on the world around me, that the end of an old cartoon from the Warner Brothers television where the image is more smaller holes, and they fall and fades to black. "
Rebecca, 30, is a rare genetic disorder called Usher syndrome type III. It is among the most cruel of progressive disease of the normal flight of nearly 16,000 people in France. And currently, there is no treatment or cure. Rebecca bravely every day life with the hope that a treatment is found, before it is too late. My family and many others are determined by our commitment with the following organizations.
An extraordinary research effort is already under way by "Usher-III of the" Vision for the hope that if a team focuses on Rebecca error. I recently spoke with Dr. David Saperstein , Scientific Director of Usher III initiative, which said that its researchers are working on a multidimensional approach to slow or stop disease progression, including the development of specific drugs and gene therapy.
In addition, the fight against blindness of the Research Foundation of a wide range of retinal degenerative diseases, including Usher syndrome, and was the first important work helped to characterize the gene for Usher syndrome Type III.
There is no time passing, where I did not recall or put into question my loss of sight or hear, but it's my life and what are the cards I was dealt. I am not frightened by the progression of my condition, but I am concerned about the things I can not hear or see.
I have the same hopes and dreams like everyone else completely secure in person and consultation and my dreams are not weakened by the gradual loss of my visually impaired and deaf, but my disability was stronger and ready for all day. When I started losing my hearing, I learned the language and have a sense of belonging to the community of deaf and hearing impaired. When I started to deal with the idea of being blind, I was looking for a specialist mobility I learned how to be with a cane, if the time I needed, I would be prepared. I do not have time, and think of all sorts of things that can happen to me. I do not have time.
I always have on my life, whatever. So it'sa challenge to get help from others. However, as my visual and hearing are again in hindsight, I always easy to ask for help. Indeed, it was very liberating. It really helped me a connection with others, and others more comfortable and open with me about their own lives. I'm incredibly lucky, have a wonderful, loving and very loyal to family, friends. More I came to myself and my own face challenges, most are your relations with others to have. What I learned is that we can not live life on our own. We all need each other to help as many different ways.
Unfortunately, many of my greatest fears have been realized. I refused, my people, if discovered about my disability. I was alone in a very strong and dark bar people who do not understand that I needed to make your stay on my side. I even take a taxi. You name it, it's likely happened to me! But I can not live my life, because I face obstacles every day. My disability has a passion and energy to live my life fully. [...]
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