arterious venous malformations?

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pictures or diagrams of arteriovenous malformations
Hope this is enough...  (+ info)

can you get a medical marijuana license for an avm(Arteriovenous malformation)?

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  (+ info)

What are symptoms of chiari malformations?

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Just to name a few:
Headache
Dizziness
Difficulty sleeping
Weakness in arms/hands
Neck pain
Numbness/tingling in arm, hand
Fatigue
Nausea
Shortness of breath
Blurred Vision
Tinnitus
Difficulty swallowing
Leg weakness
Balance problems
*Please note this is not a full list of symptoms  (+ info)

What Is an Arteriovenous Malformation (AVM)?

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how dangerous! Im a 32 years male!!
A cerebral arteriovenous malformation (AVM) is a congenital disorder of blood vessels within the brain, characterized by tangle(s) of veins and arteries. While an arteriovenous malformation can occur elsewhere in the body, this article discusses malformations found in the brain  (+ info)

If you had a baby and it had severe malformations would you have any legal right to put it to sleep or ?

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It is an odd subject but if you were the parents of a newborn with severe genetic malformations such as elephantiases or holoprosencephaly. Would you have any legal right to have the baby's life terminated just on the grounds that it will probably have a horrid life ? Like a mercy killing.

note : I am just curious if this has ever been brought up in court or anything I don't plan to have kids (much less with severe genetic defects) anytime soon)
"I don't plan to have kids (much less with severe genetic defects) anytime soon"
not planning on having kids is one thing, but you cant really plan on having a "normal" child.... just saying....

and i dont think that you are allowed to kill ur baby for being deformed.....  (+ info)

Arteriovenous Malformation (AVM) in the uterus...?

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I was diagnosed with Arteriovenous Malformation (AVM) in the uterus in Oct. the doctors said that it may or may not allow me to carry a child in the future. I have research this topic and found out that it may cause you to hemmorage.Just wondering if anyone had heard of this or what it can cause. Thanks!
~Joanna
Be educated about what the doctors tell you. I knew a woman who went into the hospital to have her second child and had a uterine artery tear and hemorrhage. she kept telling the doctors that this pain was different and something was wrong, but they just get giving her pain medicine. Finally the artery ruptured and she was rushed into surgery where they found a liter of blood inside the abdominal cavity. she had to have transfusions and died twice on the table, obviously they told her she can't have any more kids. just be careful and don't take what the doctors say lightly. good luck.  (+ info)

arteriovenous malformation?

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I want to know everything about this case arteriovenous malformation
If there is a process of how the ratio of success Please rapid reaction Please
  (+ info)

Can a person have Down's syndrome and NOT have the facial malformations associated with the syndrome?

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yeah, my ex-boyfriend is one of them!  (+ info)

Can Black Cohosh cause birth defects/malformations?

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I took black cohosh the first 3 months of pregnancy and I am scared to know that my baby will born with defects/malformations. Please help me.

Read link

http://www.naturalchildbirth.org/natural/resources/labor/labor38.htm
I took them on my own. I am scared. Please help.
I took them on my own. I am scared. Please help.
The only cases where issues of Black Cohosh came up regarding heart defects were either the doctor didn't know any cause so chose to blame the herb OR the woman took very large doses (way over thei recommended dosage). It still may not be the herb involved. This was discussed as a letter in one of the medical journals. I think you are fine provided you use only the amount recommended by your midwfe.  (+ info)

Know anything about Chiari malformations?

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I have an Arnold Chiari Malformation, type 1. My son's biological sister got diagnosed with the same thing last month. We're trying to find statistics on how rare it is, how many people per thousand are diagnosed, or whatever. And we're also wondering, is it genetic or hereditary? Links appreciated.
I saw a special on that about a year ago...
I remember that they weren't sure how rare it is, but that it seemed to be more common than had previously believed and that it did seem to run in families.

Best of luck!  (+ info)

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