| Q. | Is this normal for a Beta fish? | Related Search: Fish | | | The fish bowl seems to have bubbles formed on the corner of the bowl. Every 2 or 3 days i change the water and the same thing happens.The fish is by itself, no other fish are in the bowl. I have never had a beta fish before so i'm not sure if i should be worried. Also, I'm not sure if its a male or a female. The fish is regularly fed with pellets. Any other info i should know about beta fish??
--thanks
| | A. | This is probably the "bubble nest" it's what male bettas create to protect it's eggs while they're maturing. This happens with male bettas with or without a female betta and means that your betta is pretty healthy. Only male bettas do this so safe bet is that your fish is male...these fish are most commonly sold male in pet stores...they definately need to be kept alone! Hope this helps! | | | |
| Q. | My email settings somehow switched to something called original yahoo. How do I get my normal settings back? | Related Search: Other - Yahoo! Mail | | | There are no beta icons anywhere on my format since it is so old. Does anyone know anything about this. I have tried pressing help but I couldn't find anything related to this. An ad for a more advanced form of yahoo email had popped up when I clicked the mail icon and I had pressed go back to original at&t yahoo mail and I think that I have the 1994 version now so there are none of the newer feature buttons or links in my inbox. How do I get back to my normal email settings?
I don't have an upgrades feature or any of that since I am stuck in the older version.
after that there the same stuff is in the top right corner and no yahoo beta. there are categories though such as
mail management
personalization
and delivery service
none of which relate to yahoo beta
the only selectons in the top right corner
My yahoo
Yahoo
Options
Sign Out
Help
and that's it before and after i press the options butt on they are still the same.
| | A. | Try doing a system restore back to a date when you know your yahoo e-mail was working the way you prefer | | | |
| Q. | What does it mean if HCG levels started off rising quickly but have slowed way down? | Related Search: Pregnancy | | | At 6w4d, I had spotting and cramping and I went to the ER. They tested my HCG level and it was at 33,000. I went for a follow up blood test at 6w6d and it was 38,000. I went for an ultrasound at 7w4d and the heart was beating at 156bpm and the doctor said everything looked good but wanted me to go for one more round of blood work. Later that evening I took another beta HCG test and my level was at 57,000. At 7w6d, I took another blood test and it had only rose to 63,000.
It seems with the initial level of 33,000, my levels were doubling as normal, but have now slowed to a doubling time of approx. 10 days. Has this ever happened to anybody? What does it mean when they start to slow down this early before the placenta forms, but the ultrasound still looks good?
| | A. | I know it can take 4 days for hcg to double once you get above 6,000, but 10 days seems a little long. Since you've seen a good strong heartbeat I would assume everything will turn out fine. Either way, try not to worry. | | | |
| Q. | After I had an episode of thyroiditis (Hyperthyroid oriented) I am NOW suffering from itching, is this normal? | Related Search: Other - Diseases | | | Last year I took beta blocker 50 MG a day (Metoprolol) &
10 MG a day of Methimazole, I took these meds from July 2007 to December of 2007. My last blood labs came back very normal as far as my TSH, T3, & T4 levels.
But now after I stopped all the meds it has been a full month and half that I am stil ridiculously itching everywhere. I never ever had this problem before but now I'm just icthing everywhere my hips, in between my toes, my hair, my hands are sore and red from itching. I have bought every Gold Bond cream & powder to tone down the irritabilty of my itching but has anyone else suffereed form this and if so will this icthing subside because I WON'T take another med like Claritin and then worry about sparking my second hyperthyroid episode.
I don't even itch my skin that hard but continously suffering like this is not helping me function in life. Is this a residual effects from the generic meds I was given during my thyroid episode?
| | A. | Your thyroid hormones are probably skyrocketing since stopping the meds. Your test results were normal because the meds were working for you, not because you were cured.
When your thyroid hormones increase or decrease suddenly, you get the all over, full body, no relief itching.
Go back to your doctor, get new blood tests to see where you are at, and get back on your meds. | | | |
| Q. | Is This A Scam- Yahoo's report form does not work? | Related Search: Other - Yahoo! Mail | | | The All-New Yahoo! You Must Be A Part Of It To Avoid Your Yahoo Account To Be Closed
With the all-new Yahoo! Mail Beta you can Fill the Informations Below To Verify Your Account ,PleaseThis For Your Benefit. Read Below To Understand More.
Yahoo User
Due to the congestion in all Yahoo users and removal of all unused Yahoo Accounts, Yahoo would be shutting down all unused Accounts, You will have to confirm your E-mail by filling out your Login Information below after clicking the reply button, or your account will be suspended within 24 hours for security reasons.
* Username: .................................
* Password: ...................................
* Date of Birth: ................................
* Country Or Territory: .................................
After following the instructions in the sheet, your account will not be interrupted and will continue as normal. Thanks for your attention to this request. We apologize for any inconveniences.
Warning!!! Account owner that refuses to update his/her account after two weeks of receiving this warning will lose his or her account permanently.
| | A. | The online report form doesn't work most of the time,try using>first click on full headers and then frwd the letter [Link] . If it is a yahoo address they can help but other servers have their own abuse adddresses to us for reporting spoof/fraud/scams/spam/ Google has been the most helpful and easiest to report to. Like the others said never give out personal info to letters like this.You can check where it came fromby finding the originating IP ###s in the full header and then go to>[Link] and at least see what country it came from. | | | |
| Q. | Scientific evidence in favour of Sigmund Freud - your opinion? | Related Search: Psychology | | | Most of the critiques of Freud one reads nowadays are from people who
favor a reductionistic view that equates mind and brain and views
phenomenological exploration of the inner life of human beings as
inherently unscientific.
Evidence in favour of Freud comes from the field of
Neuropsychoanalysis:
Neuropsychoanalysis and benefits of the usage of reconstruction as an
intervention (Mitchell Slutzky, PhD, Geriatric Psychologist)
"[...] I want to distinguish between new models that reject the
importance of unconscious factors from those that continue to hold
these forces central to the change process. [...] as a whole,
psychoanalysis is losing effectiveness when it denies unconscious
motivations.
One of the most striking omissions from current psychoanalysis,
including problems with relational treatment models, is the omission
of the use of reconstructions in interpreting what could have
potentially occurred during preverbal phases of development, or which
have been "forgotten" after a severe trauma. To support this
assertion, I refer to the development of the brain from birth through
age 5 as having a developmental sequence that his just now becoming
fairly well understood. In addition, I will describe the effects of
trauma on the memory centers of the brain. Finally, I will
demonstrate the value of reconstruction, especially when memories are
not encoded or retrievable from the hippocampus. For this I will draw
upon my own clinical experience in treating patients with dementia
using a neuro-psychoanalytic approach.
At birth, an infant has a fully functioning amygdala and
hypothalamus, with most processing going upwards from the amygdala to
the right frontal lobe. The amygdala stores information in
fragmentary forms that have emotional valence indicating whether a
perception is of something safe, dangerous, appetizing, etc. This
knowledge, more emotional than cognitive, continues to play an active
role throughout human development. Next online, beginning at
approximately 3 months, is the hippocampus, a structure necessary for
more factual-based knowledge. Even so, it relies extensively upon
feedback from the amygdala which provides the emotional significance
to the fact. It should be noted that the hippocampus does not rely
upon verbal processing until much later, around the age of 12 months,
although precursors of this can be found much earlier in that infants
can respond to their names at somewhat earlier ages. Until about five
years of age, the right hemisphere remains the dominant hemisphere
for most processes. It is only after that time that the left
hemisphere -- particularly the left temporal lobe -- matures
sufficiently to allow for finer discriminations of language. From
this point forward, he left hemisphere becomes the seat of our
conscious thought while the right frontal lobe seems to play an
active role in whether thoughts and feelings are acknowledged or
repressed.
One more feature of brain processing needs to be elaborated at this
point. When undergoing a severe trauma, a person may respond by
activating the fight-flight response, corresponding to an increase in
cortisol, a naturally occurring steroid that allows for a sustained
release of energy. Unfortunately, prolonged exposure to cortisol has
deleterious effects on the hippocampus, destroying its overall
functioning. This effect does not become noticeable until senescence.
Another normally occurring substance, beta-endorphin, is released
when the person is so overwhelmed that he/she could neither fight nor
flee. Beta-endorphin dulls physical pain while erasing memory of the
event from the hippocampus. Nevertheless, the emotional, fragmentary
memory remains stored in the amygdala.
In individuals with Post-Traumatic Stress Disorder, flashbacks occur
when some fragmentary memories are triggered. Cortisol becomes hyper-
secreted in a moderate traumatic recollection. Beta-endorphin becomes
hyper-secreted in more severe traumas, leading to dissociative states
and even to dissociative identity disorder, a condition in which the
recall of the trauma is split off into fragmentary selves who are
often completely unaware of the existence of each other.
From the above discussion, it is clear that there seems to be some
correlation between Freud's psychosexual stages, and the sequence of
brain maturation. I want to add that these dates are very general,
and have not been referenced for this entry. Nevertheless, I refer
you to the works of Allan N. Schore, a developmental psychoanalyst
who has had an extensive impact on the analytic community by
demonstrating the relationship between normal brain development and
emotional development, as well as ways in which the brain develops
poorly in response to trauma and non-optimal attachment
relationships. Dr. Schore is currently researching the effects of
affect regulation actual brain structures and function. His work
clarifies many of the brain connections summarized here. He is a true
pioneer in the field of neuro-psychoanalysis. My work in dementia has
been greatly influenced by his theories. In contrast to Schore,
however,my own work focuses more on the limbic structures than it
does on the right frontal lobe. What I'm presenting here is my own
theory, in turn influenced by Schore, Joseph LeDoux, Antonio Damasio,
and Rhawn Joseph, among many others.
Since much of what can go wrong in human development takes place
prior to verbal encoding, and since trauma often leads to an erasure
of memory, or prevents the conscious memory formation from occurring
in the first place, it often becomes necessary to rely upon the
fragmentary memories stored within the amygdala in order to
reconstruct the traumatic events.
I myself rely very strongly on reconstruction, perhaps more than most
others in the field need to, because I specialize in the treatment of
people with dementia. In my clinical experience, there are many
people with dementia who have a relatively intact the amygdala with a
relatively damaged hippocampus. Their frontal and outer-temporal
lobes tend to be relatively well preserved, so they can talk about
their experience and use reason to improve their understanding of
their feelings. Performing the role of an auxiliary hippocampus, I
help my patients take fragmentary emotional responses and
recollections, assemble them into a whole, and repeat this over time,
so that it gets into long-term memory despite the poorly functioning
hippocampus. Usually, these individuals have had severe traumas in
their lives, which led to hypervigilance and an over-active danger
alarm. I teach my patience to contain the intensity of the emotional
response while retaining the reconstructed memory, which is in turn
paired to a more adaptive emotional response.
From the above description of my technique, summarized and over-
simplified, it may be difficult to see how my work connects to
psychoanalysis. That may be because I'm leaving out the content of
the traumas, which typically have psychodynamic significance. In
fact, I find that the perception of what happened matters more than
the veridical truth. (Of course, this opens up the issue of screen
memories, a subject for a whole book on psychoanalysis and the nature
of memory itself.) It is through exploration of these unconscious
conflicts that the fragmentary recall emerges. It is through the
reconstructions that trauma can begin to be recalled in a safer
light. While the dementia is not reversed, excess disability is
diminished. These patients become less depressed or anxious, and have
improved cognitive functioning. What was unacceptable becomes more
acceptable. Using Freud's tripartite terminology, where formerly
these memories were contained in the id, they are now able to be
transformed through the ego.
In this brief summary, I am omitting many other brain structures, as
well as over-simplifying and over-generalizing the roles and
interconnectedness of those that I have addressed directly. I just
wanted to give readers of this forum a viewpoint from one who
practices psychotherapy employing an integration of neuroscience and
psychoanalysis. I hope you see that there may be benefits to such
integration, not just in expanding technique, but in validating and
building upon some of Freud's brilliant observations. His model is
gaining greater support as more is known about the function of the
brain. In this way, neuro-psychoanalysis represents the best way
forward, infusing the most comprehensive system of the mind with
empirical neuroscientific support. This enables the widening scope of
psychoanalysis to treat a greater number of disorders while
simultaneously enabling the therapist to make greater conscious
choices as to what therapeutic intervention would be most useful for
which patient. While this posting focused on the neuropsychology of
reconstruction, it obviously has much broader implications in this
emerging field of neuro-psychoanalysis."
| | A. | I am a bit puzzled how my posting to a user group on neuro-psychoanalysis got onto yahoo! answers as a question. I suppose that means people are reading the board it was posted on. It was not intended to answer a simple question about scientific support for Freud's theory. It was more of a mini paper.
Saying it simply: the field of neuroscience has many studies in support of Freud on many levels. No longer can we say that there is no such thing as "the unconscious". fMRI's, SPECT and other brain measurement of regional cerebral blood flow have yielded an enormous wealth of data on how information is processed unconsciously milliseconds before it is consciously recognized. And the information is repressed by the right frontal orbital lobe (the front right outer-part of the brain under the forehead) if deemed by that part of the brain to be too unacceptable to acknowledge. That suggests that Freud was right to see repression as a common psychological defense.
I could say more, but I have already been told I was too technical in the "question" within which I was so lengthily quoted. Wait for the articles and the book.
MS | | | |
| Q. | Prion Diseases: If I had Mad Cow Disease, would my children inherit it too? | Related Search: Medicine | | | I just heard a National Public Radio piece on prion diseases.
I learned a lot.
First I had no idea it was a protein misfolding (alpha to beta) disease (as I always thought prions were a form of viruses), and secondly when the protein combines with other normal proteins, the normal proteins are twisted out of there alph configuation to become beta sheets. How fascinating!
My question is this. If I were injected with an extract from a cow that was known to have Mad Cow Disease, would this prion disease be passed to my children (assuming I had no previous genetic defect predisoposing me to prion diseases), or would it end with me, dispite the fact that I fathered children while I was carried the prion.
This wasn't made clear to me in the NPR piece, which really dealt with a predisposing prion disease.
Thanks for your thoughtfull responses!!
p.s. I always respond to the best answer.
| | A. | Genetic disorders that are passed down to the next generation have usually come from pas generations, you have it becuase one of your parents had, they had it because on of their parents had it, and so on. However, if the injection caused your DNA to mutate before you had kids, then yes it would be possible to pass it to your children through your genes. | | | |
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