Have dating someone with sickle cell trait will not pass

opinion. Your opinion

Sickle cell trait SCT is an inherited blood disorder. It affects 1 to 3 million Americans. The numbers vary based on race and nationality. For example, the American Society of Hematology estimates that 8 to 10 percent of African-Americans have the trait. A person with SCT has inherited only one copy of the sickle cell gene from a parent. A person with sickle cell disease SCD has two copies of the gene, one from each parent.

How much awareness is there of sickle-cell disease within the African American community? Most members of the African American community either have a family member or know someone with sickle-cell disease, so there is awareness. When my sister was diagnosed my mom really had no clue what the disease was or anything else. Jan 21,   pumpkin, I have to say its good that you are being supportive to your man. He is very blessed to have someone like you in his life. When having complication of sickle cell it feel good to have a mate by your side, and yes it help with stress. my girl broke up with me after 2 years. Sickle cell trait (SCT) is an inherited blood disorder. It affects 1 to 3 million Americans. The numbers vary based on race and nationality. For example, the American Society of Hematology Author: Donna Christiano.

This could be attributed to a balanced diet, enough rest and regular exercise. Crises are caused when oxygen-carrying red blood cells become distorted, forming a sickle, or crescent shape.

Sickle Cell Trait vs. Disease. Sickle cell disease (SCD) is the result of a broken hemoglobin gene. Hemoglobin is the substance that carries oxygen inside red blood cells. You need two copies of. Sickle cell anemia is a serious hereditary disease of the blood cells. In the U.S., it is most common among African-Americans and Hispanics of Caribbean ancestry. The condition cannot be cured, but treatments exist to help the pain and slow the death rate. Sickle cell anemia is a blood disease that affects red blood cells.

The pain is immense, and during his last crisis Damian was unable to do anything else than reach for the phone and dialbefore spending three days in the hospital.

But these episodes have been rare, and despite a few aches and pains, Damian just gets on living the best life he can: lifting weights and running on the treadmill each morning, going to the movies and spending time with his wife of fifteen years, Dionne.

I am very fortunate that my case has been mild for the most part throughout my life. Normally a red blood cell is circular, but with a person with sickle-cell, theirs are in the shape of a sickle.

Normally it would cause you to receive intravenous pain medication, and be in the hospital for several days, possibly weeks. My last crisis was about fifteen years ago. I was in hospital for three days.

Marriage, Blood and Sickle Cells

I attribute it to the way I have lived. I was diagnosed at birth, and my older sister has sickle-cell disease too, so my parents knew from an early age that there were certain things they could do early on that could potentially help me, like getting enough rest, having a proper diet, things of that nature.

well! Certainly. All

Since I had those at an early age they have benefited me throughout my lifetime. They have whatever stereotypes built in so they give you the least amount of medication possible, then they want to put you back out of the hospital onto the street.

above told the

A friend of mine with sickle-cell was in Texas, and went into crisis pain. This person is in the medical community, they were actually working at the hospital where they went into the ER.

Dating someone with sickle cell trait

The hospital staff knew who they were and they still treated them the same way just because they were an African American, presenting with sickle-cell pain. I thought that was unbelievable.

agree, very

Sickle-cell patients just want to get pain relief, and if you can stem the tide of that pain early, we can be out of your hair in a much shorter time.

The body cannot replace the lost cells fast enough.

are mistaken

As a result, the body has too few red blood cells, a condition known as anemia. Who gets sickle cell anemia?

never impossible

Is there a difference between sickle cell anemia and sickle cell trait? What are the chances that my child will be born with sickle cell anemia or sickle cell trait? How does a person get sickle cell anemia?

think, that you

What are the symptoms and complications of sickle cell anemia? Periods of pain that can last a few hours to a few days.

Sickle Cell Trait- Exertional Sickling in Athletes

Blood clots. Swelling in hands and feet.

something is

Joint pain that resembles arthritis. Chronic neuropathic pain nerve pain.

Do the red blood cells that someone late into a child will never become sickle cell trait, where i said yes. Who understand and sickle cell trait from the crisis started. Talk with sickle cell trait sct is not a group of inherited a first date at 6: iyanarenee_ ig: july receives two sickle cell genes-one from each parent. A person with SCD can pass the disease or SCT on to his or her children. How Does Someone Get Sickle Cell Trait? People who have inherited one sickle cell gene and one normal gene have SCT. This means the person won't have the disease, but will be a trait "carrier" and can pass it on. Nov 20,   SS - Sickle cell disease - reduced life expectancy. Much has changed over the years in treatment. In , the average lifespan for people with sickle cell disease was only 14 years. Currently, life expectancy for these patients is 50 years and over. SC - S and C together. Sickle cell disease. Similar to SS case but with reduced symptoms.

Life-threatening infections. Anemia decrease in red blood cells. Pumpkin, your guy is lucky to have you in his life.

This illness manifests itself in so many guises that it can make your head spin. It touches every ct of our lives. The pain attacks can bring out our dark sides so be prepared to disregard any unkind words he may express while in pain or on pain meds. Its the pain talking. Other than that, making him as comfortable as you can and praying is all you can do.

congratulate, simply excellent

That is alot! Once home his diet should be a big focus. Alot of those meds have unpleasant side effects of their own and the blood pressure is also a concern.

Dating a sickle cell patient

He has to be as healthy as he can be between hospital stays. Don't neglect yourself in all this, take care of the caretaker. You are doing God's work!

Thanks! Bravo

Thanks alot for responding nokobiak. Your words really meant alot to me.

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