Meniere’s syndrome is an inner ear disease characterized by fluid accumulation in the membranous vagus. It is characterized by sudden onset of vertigo, tinnitus, deafness or nystagmus as the main clinical manifestations, and vertigo has distinct episodes and intervals. The symptoms vary from person to person. The main symptoms of the attack phase are: the attack is sudden and can occur at any time, even after going to sleep. The most common symptoms are: when the patient opens his eyes, he feels that the house or surrounding objects are rotating, and when he closes his eyes, he feels that his body is rotating, and when the vertigo is strong, the patient may suddenly fall to the ground. Most of the patients lie still with their eyes closed and are afraid to turn their head and body if they open their eyes or turn their head during the attack. Most patients have unilateral tinnitus and deafness during the attack, but a few have bilateral attacks. About 25% of the patients have tinnitus and deafness before the attack, and they get worse after the attack. The remaining approximately 25% develop tinnitus or deafness gradually after the attack. The deafness is neurological in nature, and the tinnitus is aggravated by the intensity of the attack. The attack is often accompanied by a series of symptoms such as not daring to open the eyes, nausea, vomiting, pallor, sweating, even diarrhea, and low blood pressure in most cases. Some patients have headache. There are two forms of intermittent episodes: one in which the vertigo and accompanying symptoms suddenly disappear, and one in which the vertigo gradually changes to dizziness and gradually subsides. The length of intervals in Meniere’s disease varies from months to years, and each attack and its degree varies. And hearing gradually decreases with the number of episodes.