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There are a number of genetic red blood cell disorders known as sickle cell disease. One of the most dangerous forms of sickle cell anemia is termed sickle cell disease.

People of African or Caribbean ancestry are more likely to be diagnosed with sickle cell disease.

These abnormally shaped red blood cells may create issues since they don’t survive as long as healthy blood cells and can clog blood arteries in people with sickle cell disease (SCD).

Many symptoms of sickle cell disease may be alleviated with medication.

A simple blood test is all that is needed to diagnose SCD. In most cases, it is discovered during standard newborn screenings at the hospital. Prenatal diagnosis of SCD is possible, as well.

The earlier a kid with SCD is diagnosed and treated, the lower their risk of infection and other health issues will be.

You may get tested for sickle cell disease by contacting your local sickle cell group.

A cure for sickle cell disease is our ultimate objective at the University of Pittsburgh, where we’re exploring innovative and effective treatments for the condition.

Knowing more about sickle cell disease’s core molecular processes and difficulties now allows us to focus our research on clinical concerns like creating specialized treatment regimens and gene-based medicines that will eventually lead to a cure for the condition.

You can help the Cure League discover a cure for sickle cell disease by taking part in a clinical study, which is just one of the numerous ways you can assist.

Sickle Cell disease treatment in United Kingdom

Sickle cell disease is an inherited blood disorder that affects red blood cells. Sickle-shaped erythrocytes are unable to deliver oxygen efficiently around the body and tend to block small blood vessels, which can lead to pain, organ damage and infections.

In the UK, there are thought to be around 15,000 people with sickle cell disease (SCD) or variant SCD. The most common type of SCD in the UK is homozygous HbSS (inheriting two abnormal genes for haemoglobin S). Other types include sickleHaemoglobin C Disease(HbSC), where a person inherits one gene for HbS and one for another abnormal form of haemoglobin called HbC; this makes their condition more mild than those with HbSS sickle cell anaemia .

People from African descent are particularly affected by SCD as it’s estimated that 1 in 300 black babies born in England will have the condition . However , due largely to increased awareness about antenatal screening tests , many more cases of SCD are now being detected early so treatment can begin immediately after birth.

Although there’s currently no cure for SCF, patients receive regular hospital check ups and transfusions throughout their life as well as medication such hydroxyurea which helps reduce episodes of pain crisis . With proper medical care , people with sickle cell disease can enjoy long productive lives.

If you need to pickup your free test, you can get fill a form and get it through the post. Most Post offices in the UK will be able to provide you with a form that you can fill straight away and get your kit in the post.