Most people with familial Mediterranean fever experience their first symptoms during childhood. These symptoms occur in attacks that last from one to three days with arthritic attacks lasting for weeks or months.
The following are the signs and symptoms of familial Mediterranean fever:
As Familial Mediterranean Fever is hereditary, it is unpreventable.
There is no cure for familial Mediterrenean fever although the signs and symptoms can be treated.
Medications given include drugs like Colchicine , rilonacept ( Arcalyst) and anakinra (Kineret) that reduce inflammation and prevents frequent attacks.
Side effects of Cochicine are common and they include blaoting , abdominal cramps and diarrhea.
6 Lifestyle and Coping
Lifestyle modifications are necessary in order to cope with familial Mediterranean fever.
Living with familial Mediterranean fever can be annoying especially since attacks can happen at any moment.
People affected can cope by doing the following:
Learning about familial Mediterranean fever
Joining support groups or talking to people who are living with this condition or those that know more about it
7 Risks and Complications
The risk factors of familial Meditarranean fever include:
Having a family history of the disease
Being of Mediterranean ancestry
Several complications can occur if patient is not treated or treatement is ineffective.
Accumulation of amyloid A, an abnormal protein, in blood . This protein can accumulate in organs and can cause organ dysfunction.
Kidney damage due to accumulation of amyloid in the kidneys. This usually laeds to the nephrotic syndrome, a syndrome associated with large amounts of protein in urine. Nephrotic syndrome can further lead to the patient developing kidney failure.
Infertility in women can occur if there is inflammation the repeoductive organs like the ovaries or uterus.
Joint pain is one of the most common symptoms of familial Mediterranean fever. The mostly affected joints are the knees,ankles, hips and elbows.
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