What is familial hemiplegic migraine?
Familial hemiplegic migraine (FHM) is a rare and often severe form of migraine that is caused by a combination of genetic and environmental factors. It affects mostly women, and can be accompanied by other conditions such as stroke or epilepsy. Thankfully, there are now a number of treatments available that can help people with FHM live comfortable lives.

What Is Familial Hemiplegic Migraine?

Familial hemiplegic migraine is a rare condition that is caused by a mutation in the gene for the neurotransmitter serotonin. This mutation results in an increased level of serotonin in the brain, which can lead to headache, nausea, and vomiting. There is currently no cure for familial hemiplegic migraine, but there are treatments that can help manage the condition.

What Are The Symptoms Of Familial Hemiplegic Migraine?

Familial hemiplegic migraine is a rare condition that affects the brain and spinal cord. The disease is caused by a mutation in a gene called CACNA1A. Symptoms of familial hemiplegic migraine include: sudden, severe headache; neck stiffness; blurry vision or blindness; numbness or tingling in the arms, legs, or face; rapid heart rate; and confusion.
There is no known cure for familial hemiplegic migraine, but treatments can help relieve symptoms. Treatment options include medication, therapy, and surgery.

How Can Familial Hemiplegic Migraine Be Treated?

The cause of familial hemiplegic migraine is unknown, but it is thought to be caused by a combination of genetics and environmental factors. Treatment for familial hemiplegic migraine typically involves medication and/or therapy to reduce the frequency or severity of attacks. Some people may also require surgery to remove the cause of their headaches.

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Instant Migraine Spiritual Cure

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