What is the life expectancy of someone with Erythromelalgia?

Life expectancy of people with Erythromelalgia and recent progresses and researches in Erythromelalgia


Erythromelalgia is a rare and chronic disorder characterized by intense burning pain, redness, and heat in the extremities, typically the hands and feet. This condition is often triggered by heat, exercise, or even emotional stress. While erythromelalgia can significantly impact a person's quality of life, it is important to note that it does not directly affect life expectancy.



Erythromelalgia is a chronic condition that requires ongoing management and treatment to alleviate symptoms and improve daily functioning. The severity of symptoms can vary greatly among individuals, ranging from mild discomfort to debilitating pain. The condition can be primary, meaning it occurs on its own, or secondary, where it is associated with other underlying conditions such as myeloproliferative disorders or neuropathies.



While erythromelalgia itself does not pose a direct threat to life expectancy, the impact it has on an individual's well-being can indirectly affect their overall health. The chronic pain and discomfort associated with erythromelalgia can lead to sleep disturbances, anxiety, depression, and reduced physical activity. These factors can contribute to a decline in overall health and potentially increase the risk of developing other health complications.



Managing erythromelalgia involves a multidisciplinary approach, including medical interventions, lifestyle modifications, and psychological support. Medications such as vasodilators, anti-inflammatory drugs, and nerve pain medications may be prescribed to help alleviate symptoms. Lifestyle modifications may include avoiding triggers, maintaining a cool environment, wearing loose-fitting clothing, and elevating the affected limbs.



It is crucial for individuals with erythromelalgia to work closely with healthcare professionals to develop a personalized treatment plan that addresses their specific needs. Regular follow-ups and adjustments to the treatment plan may be necessary to manage symptoms effectively.



While erythromelalgia can significantly impact daily life, it is important to focus on improving quality of life rather than dwelling on life expectancy. By effectively managing symptoms, seeking appropriate medical care, and adopting a holistic approach to well-being, individuals with erythromelalgia can lead fulfilling lives.



Support networks and patient communities can also play a vital role in providing emotional support, sharing experiences, and offering coping strategies for individuals living with erythromelalgia. Connecting with others who understand the challenges of the condition can help reduce feelings of isolation and provide a sense of belonging.



In conclusion, while erythromelalgia is a chronic and potentially debilitating condition, it does not directly impact life expectancy. With proper management, treatment, and support, individuals with erythromelalgia can lead fulfilling lives and focus on improving their overall well-being.


by Diseasemaps

Erthromelalgia cannot kill you however people have committed suicide due to the severe depression of living with this disease everyday and the fact that most people that are diagnosed are told they have a rare disease and when you have no one to talk to and no one who understands what you're going through that makes it very difficult

9/16/17 by Jeff 3050

There is no "standard' life expectancy. It can depend on how long the person has been afflicted and what other conditions they might have.

12/27/17 by mleaver 2500

I don't think this disease medically shortens the life expectancy of a sufferer

4/4/18 by Alys 2500

I think people with EM live about the same amount of time as those without it. I think depression and the resulting shorter life expectancy is probably the worst complication endangering our lives. Recent vascular studies linking it with Raynauds and they feel that it is reversible in some cases.

1/18/21 by Kathy Vanicek 2500

I have been diagnosed with EM for over a year. I have a severe case. People who feel the need to separate increase risk in suicide from EM mortality don’t seem to understand that if your face feels like it’s melting, you’d want to die to. Many clinics won’t treat em patients. Saying they don’t want to touch us. Others act like they know and they don’t (like most of these commenters). Let me be VERY clear. EM research is extremely close to none. Having EM means either waiting on a genetic “cure”, waiting for your idiopathic secondary cause to be diagnosed, waiting for your idiopathic secondary cause to be treated, or waiting for proper pain management. The only clinic that I’ve talked to that even offers intravenous lidocaine is Boston pain clinic. Yes. There’s obviously an increased mortality. To say otherwise is ignorant.

8/14/21 by saguaros 3000

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