valacyclovir and sickle cell anemia

Speaking very generally, if you carry sickle cell trait and your wife carries sickle cell trait, your child will have a 50% chance to carry sickle cell trait, a 25% chance to get sickle cell anemia, and a 25% chance to get neither the trait or the illness. But read the following carefully because that is a general statement only and you need to be more specific. http://www.sicklecellsociety.

At one point, when she was young, they thought it was sickle cell until they did the test and found it to be negative. She was carrying the sickle cell trait though. She has all the symptoms of an anemic, but with normal iron levels. Iron was not helping her either. I think that the blood cells are too small to carry the oxygen and the reserve of iron is normal because it was enough for her small red blood cells.

s oldest son from a previous relationship has sickle cell anemia, I assume hubby and ex were both carriers. I was tested with my first son and I'm not carrier, our son together doesn't have it. Let your doc know your partner is carrier and that you'd like to be tested.

it said that if only one parent has the sickle cell gene only the baby will be a carrier (sickle cell trait) he does not have sickle cell disease. No side effects. If both parents have it then the baby has it also. But still it the baby has ir not all experience pain or any type of symptoms.

I found out that I am a carrier for Sickle cell anemia and that if my partner has it to my son can get it on top of the fact of there being a chance of him being a premature baby he may now have to deal with this.I have also been hospitalized for the past week because I have a thinning cervix. I don't think I can handle anymore bad news.

The doctor called and said she looked at my blood and i need to get tested for sickle cell anemia. If i had that wouldnt i know? Has anyone gone through this? Im terrofied somethings wrong with me!

Hello, Microscopic hematuria can be due to urinary tract (bladder) infection, swelling in the filtering system of the kidneys ,stone in bladder or in a kidney, blood disease, like sickle cell anemia, certain medicines and tumors in the urinary tract. You have already undergone cystoscopy which has ruled out most of the cases. I suggest you to get done an ultrasound abdomen to look for any kidney stone and blood tests for sickle cell anemia. I hope it helps.

Hi, so I've had CF all my life but recently I've noticed my blood work is lacking in the statistics I need. It's always been pretty bad but never this bad. After further investigation my doctor diagnosed me with Sickle Cell Anemia but I'm wondering if that's even possible! Since they're both inherited you'd think you'd only get one but I don't know. Is it possible, and if not, should I get a second opinion?

s the reason I keep miscarring I know some pll wit sickle cell and have had successful pregnancies but I have yet to find some1 with sickle cell and only have 1 ovary and have had a successful pregnancy so it's like wat do you do to keep this 4rm happening

vgnextchannel=aba462221d948010VgnVCM1000000e2015acRCRD I found this story to be very encouraging... this child has never had a crisis... i dont know a lot of sickle cell anemia...especially for babies, its does sound very scary and i hope your baby doesnt have it :( i was able to observe a surgery with a young man who had the disease and the Dr they brought on for him was awesome and he taught me a lot about what all can occur... but like i said i really wasnt aware of the effects in babies...

Are you associating the erections with sickle cell anemia? My son had erections from the time he was a baby and my pediatrician just said it was totally normal. Didn't your husband have erections when he was a boy?

The renal function and liver function needs to be checked as also electrophoresis of hemoglobin to know whether there is thalasemia trait or sickle cell anemia. You need to see if there is vitamin B12 deficiency. Once the cause is found and corrected, anemia will control by itself. Please consult your PCP for primary examination followed by proper referral to a hematologist. Take care!

Epistaxis or persistent nose bleeding is indicative of systemic causes in absence of previous history of injury or surgery to nose.It can happen in coagulative disorders like Sickle cell anemia or von Williebrand's disease or Hemophelia,where coagulation pathway is abnormal and bleeding persists despite of measures taken.Situations like panic or nervousness/ anxiety,sneezing may also trigger nose bleed.

Hello, Microscopic hematuria can be due to urinary tract (bladder) infection, swelling in the filtering system of the kidneys, stone in bladder or in a kidney, blood disease, like sickle cell anemia, certain medicines and tumors in the urinary tract. You have already undergone cystoscopy which has ruled out most of the cases. I suggest you to get done an ultrasound abdomen to look for any kidney stone and blood tests for sickle cell anemia. I hope it helps. Take care and regards.

I suggest you to consult a urologist and get done an ultrasound abdomento look for any kidney stone and blood tests for sickle cell anemia. You also need to get urine examination and urine culture and cystoscopy done from a urologist. It is very difficult to precisely confirm a diagnosis without examination and investigations and the answer is based on the medical information provided. For exact diagnosis, you are requested to consult your doctor. I sincerely hope that helps.

I do know that having a first degree relative increases the chances of having it when you're older, but not sure the percentage.

Hello, Microscopic hematuria can be due to urinary tract (bladder) infection, swelling in the filtering system of the kidneys ,stone in bladder or in a kidney, blood disease, like sickle cell anemia, certain medicines and tumors in the urinary tract. In your case kidney stones and urinary tract infection have been ruled out. I suggest you to get done an ultrasound abdomen to look for any kidney stone and blood tests for sickle cell anemia. I hope it helps.

You need iron to produce red blood cells. So without iron, you develop anemia (low red blood count) and it makes you feel a little breathless because red blood cells carry oxygen and you have to breathe a little harder and your heart beats become more noticeable. So it sounds like your doctor is on this and has increased your iron supplements? Anemia is very common in pregnancy, by the way, and usually responds pretty quickly to treatment with oral iron supplements.

Im freaking out I am a first time mom 18yrs.old and 7wks.

I have sickle cell "anemia" so ik what its like to be anemic. ***** to be tired all the time.

sickle cell anemia, and Beta thalassemia and Herediatary Persistance of Fetal Hemoglobin and the Acquired ones are: paroxysmal nocturnal hemoglobinuria, aplastic anemia, thyrotoxicosis hepatoma and choriocarcinoma. Are you from the mediterranean originally or is your family? Are you African American? Did you have a complete blood count done? How high was the hemoglobin F level? Do you feel tired all the time or bleed anywhere?

why can sickle cell disease patients NOT receive procrit therapy? Is it because there rbc's are already being attacked?

Valacyclovir and sickle cell anemia

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