Femepa organizes a course on the assembly and maintenance of

Víctor Rubio, director of communication and marketing of the metal employers' association, remembers that the degree allows you to obtain a professional card in a sector with very high labor demand. Go to download The Federation of Metal and New Technologies SMEs of Las Palmas (Femepa) organizes from June 27 to September 27 a course on the assembly and maintenance of heating installations that entitles you to carry out professional work in the area of ​​plumbing, air conditioning and refrigerators , calorific. Free of charge, this 500-hour course, one hundred and twenty of them internships, is aimed at unemployed people who, in just three months, can obtain a degree that qualifies them to sign installation bulletins, and they also obtain fifty percent of training to obtain a higher qualification. According to Víctor Rubio, director of communication and marketing of the metal employers' association, this is a degree with high job demand in the tourism sector. Objectives and requirements The objective of the course is to develop the ability of students to carry out assembly, maintenance and repair operations of heat production facilities and their transmission by fluids, in accordance with the assembly and maintenance processes and plans, with the required quality. complying with current standards and regulations, under conditions of personal and environmental safety.



To access the course you must be registered as a job seeker in the Canary Islands Employment Service and have some of the following qualifications: ESO, Level 2 professional certificate, Level 1 professional certificate from the same family and Professional area, 2nd year of BUP , Title of Technician or Auxiliary Technician, access test passed to medium-level training cycles, University access for those over 25/45 years old or key level 2 competencies.They demand specialized residences to care for ALS patients Currently there are about a hundred people WhatsApp Number List affected by ALS in the Canary Islands Currently there are about a hundred people affected by ALS in the Canary Islands Pilar Fernández Aponte, member of the Spanish Association of Amyotrophic Lateral Sclerosis, points out that, throughout their lives, 5,000 Canaries will suffer from a disease whose origin is still unknown. Go to download The Spanish Association of Amyotrophic Lateral Sclerosis (adELA) requests the creation of specialized residences for patients with Amyotrophic Lateral Sclerosis (ALS) capable of meeting their needs as a result of the development of the disease. As indicated by the member of the Association, Pilar Fernández Aponte, neither in the Canary Islands nor in Spain are there specialized residences for patients who require special care twenty-four hours a day.







These residences presuppose the training of personnel who must be trained to attend to needs that are not exactly the same as those of other people who require care. In the Canary Islands there are currently about a hundred people affected by a disease that is “a lottery” because, in most cases, it is unknown how it occurs. Throughout their lives, more than 5,000 canaries will develop ALS. This neurodegenerative disease has no cure and the average life expectancy of patients is two to five years after diagnosis. World Amyotrophic Lateral Sclerosis Day Last Tuesday, June 21, World Amyotrophic Lateral Sclerosis (ALS) Day was celebrated. Three letters that are becoming less and less unknown to society every day and that give their name to a neurodegenerative disease that is characterized by causing progressive muscle paralysis until mobility is completely lost – only eye movement is maintained – while the mind remains intact. Currently there is no cure for ALS nor has a medication been found that is capable of stopping its development and turning it into chronic disease, so the average life expectancy is two to five years after diagnosis. The initial symptoms are usually muscle weakness in the extremities (legs and/or arms) although it can also present in other ways such as problems swallowing or vocalizing. As the disease progresses, the degeneration of the motor neurons spreads the lack of mobility throughout the body, also causing the patient to require constant attention and surveillance 24 hours a day. Faced with this situation, patients with ALS have two solutions: pay for caregivers out of their own pockets to care for them in their homes or enter a residence that can meet their needs.