Danute advised a neighbor to visit doctors: slow progression of symptoms causes undetectable disease Life



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Acromegaly is a rare endocrine disease that occurs when the pituitary gland produces too much growth hormone. This is a long-term increase in growth hormone secretion, we wrote in a report distributed by the Kaunas clinics.

“The most common symptoms are enlarged arms, legs and tongue, altered facial features. Frequent headaches, fatigue, sweating, severe snoring, increased spaces between the teeth are typical, “says Robertas Knispelis, a doctor at the Endocrinology Clinic of the Kaunas Clinics.

Acromegaly is usually diagnosed in middle age, as happened to Danute, a patient at the Kaunas clinics. According to her, the first changes appeared on the face.

“The skin got rougher, deeper wrinkles appeared. I started to feel worse, my blood pressure went up, I started to suffer from insomnia, I gained weight quickly, I was sweating a lot, I lacked strength and was often sad, says the patient. – Posterior enlargement of the extremities, lower jaw, nose and internal organs. For those unaware of this disease, it probably seemed that he was consuming alcohol. It was painful to look in the mirror. “

Unfortunately, the diagnosis of acromegaly takes time. The disease is usually diagnosed 7 to 10 years after the onset of the disease. According to the endocrinologist, this is because people do not recognize the disease due to the slow progression of symptoms. The good news is that the disease can be cured or controlled.

The disease is usually diagnosed 7 to 10 years after the onset of the disease.

“Surgical, medical or radiation treatment is used to treat the disease. It is possible to control it, although most patients have to apply a combination of treatment methods, and medical treatment can last more than a year, “says R. Knispelis.

The medication for the patient returned results immediately. She felt better, and after three months, the woman became more energetic. “It seems like there was no anxiety or sadness left inside, which oppressed me for a long time,” Danutė is happy.

The woman says she is partly grateful for her illness. “It just caught our eye then. Do I live how I want? What talents have I brought to life? Do I take care of them? In search of answers to questions, I began to grow in the realm of personal development. Previously, only the body grew , Danutė smiles. – I completed many courses, changed my address and got to know each other again. I became interesting not only for others, but also for myself. “

The woman currently represents the Society for Acromegaly and Pituitary Diseases.

According to endocrinologist R. Knispel, it is important for people to seek help after noticing changes in the body. The Center for Rare Endocrine Diseases operates in Kaunas clinics, and rare diseases are detected and treated more quickly at these centers. Professionals have great knowledge and experience, as well as the opportunity to consult directly with professionals at European and global level.

According to the World Health Organization, acromegaly affects between 40 and 70 people in a million. Every year, 3-5 new cases are diagnosed per million inhabitants.



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