Has anyone heard of a disease called “Black Ace”? if so please let me know as much info you can give.. also unsure if thats the correct name and if you know the correct name please help me out.. its a rare blood disease known to attack organs.. only 2 people in the world has this disease only one is living .. if you think you can help please get back to me A.S.A.P
Me and my friend were talking and she was saying who cares about the human body when we could care about animals. So i was like, do you know how many diseases are known to the human body? She was all like no and i was like neither do i so ANSWER!!!
thank you
how big is the gap say for a disease that is rare and a disease that is very rare?(such as Asperger’s syndrome)
2. A child is diagnosed with a rare genetic disease. Neither parent has the disease. How might the child have inherited the disorder?
(1 point)
The disorder is dominant and was carried by a parent.
The disorder is recessive and carried by both parents.
The disorder is sex linked and inherited only from the father.
The disorder could occur only as a mutation in the child because neither parent had the disease.
3. A phenotype that results from a dominant allele must have at least _____ dominant allele(s) present in the parent(s).
(1 point)
one
two
three
four
4. A phenotypic trait that results from a single dominant allele is _____.
(1 point)
attached earlobes
more frequent in its appearance
cystic fibrosis
polydactyly
My doctor just called me and said i have some rare disease that affects one of my unborn triplets. He said baby number three might not live. Baby number three is Bradon Adam. I am crying and typing at the same time . How do i tell my family and my husband. My husband was so looking forward to this if you have any comments or somthing please write i need some words of wisdom. My husband is on a work trip in chicago he will be home tommorrow Please Help For the sake of bradon adam Thank you Bye
or using other products made of cow ingredient.
Fifth Important Lesson – Giving When it Counts…
Many years ago, when I worked as a volunteer at a hospital, I got to
know a little girl named Liz who was suffering from a rare and serious
disease. Her only chance of recovery appeared to be a blood transfusion
from her 5-year old brother, who had miraculously survived the same
disease and had developed the antibodies needed to combat the illness.
The doctor explained the situation to her little brother, and asked the
little boy if he would be willing to give his blood to his sister.
I saw him hesitate for only a moment before taking a deep breath and
saying, “Yes I’ll do it if it will save her.” As the transfusion
progressed, he lay in bed next to his sister and smiled, as we all did,
seeing the colour returning to her cheek. Then his face grew pale and
his smile faded.
He looked up at the doctor and asked with a trembling voice, “Will I
start to die right away”.
Being young, the little boy had misunderstood the doctor; he thought he
was going to have to give his sister all of his blood in order to save
her.
When I was in middle school, I was diagnosed with ocd, depression, and socail anxiety disorder. In the past year and a half or so, I was also diagnosed with bipolar(2), schizotypal personality disorder, generalized anxiety disorder, and body dysmorphic disorder (I’m not to sure if that was an actual diagnosis though. My therapist said it sounds like BDD, but that it could also be from my other issues). Then, on april 3rd I got diagnosed with Ehlers Danlos Syndrome (which is a rare connective tissue/collagen disorder). Do you think having all these things wrong with me somehow makes it more possible to rare things to happen to me or common things to happen to me in a rare way? I feel like I collect diagnoses. I have an immense fear of HIV, so when I hear that having all these things wrong plus a rare tissue disorder, I’m always scared I’ll catch the disease in a “rare” way, even though I don’t have sex, do drugs or anything like that. Is my fate wacked out or something? Would you be scared if you had more than 1 rare thing going on with you? Would you feel like you were in danger or something?
Thanks!
48 minutes ago – 3 days left to answer.
Additional Details
21 minutes ago
Also, I have a learning disability. Dyscalculia (numbers/math). and my therapist thinks I also have dyslexia because I sometimes can’t process information.
Peter and cindy was already pregnant befor coming to america. although peter found aminimum wage jab, the couple has no medical insurance. during the pregnancy, cindy did not meet with a doctor. however, when the baby was born it was discovered to suffer from a rare disease. infants born with the diseas almost always die within the first few months and those that survive rarely it past their couple years. the couple wants the hospital to do all it can to save the child’s life. the hospital, knowing that the child will most likely die with or without medical intervention, is reluctant. for the moment, since the couple does not have medical insurance, they have reached am impasse.
should the hospital perform the surgery? are cindy and peter right to try and save the child’s life? if they did not wourl it be immoral?
My deceased husband was diagnosed with human parvo in 2004. He was also diagnosed with CLL in 2000. He became lukiemia free and 3 months later passed. On the death certificate it states human parvo. Not many case are known but how does a person get this disease? I just don’t quite understand it.