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Social Security denies work incapacity to a disabled person

Do not present anatomical or functional reductions that reduce or annul their work capacity. This has been the response that a 31-year-old man from Ceuta who has become disabled after being vaccinated against Covid-19 in the summer of 2021 has obtained from social security. This young mackerel has seen how his life has taken a 180º turn just a year, when he went like thousands of others when they called him to be inoculated with the second dose of the Pfizer preparation.

In less than 48 hours after administration, side effects began that were not specified in the product’s technical data sheet and that have left serious consequences to this day, making it impossible for him to lead a “normal” life. Pain, tremors, seizures, myocarditis, dysautonomia, weakness, polyneuropathies, immune disorders, myopathies, hallucinations, diarrhoea, transient ischemic attacks and even tetraparesis among a dozen other neurological and cardiological symptoms, have not been enough for the Ceuta social security can determine an anatomical or functional reduction.

The affected person affirms that he is still alive “thanks to private healthcare” since with more than 20 emergency admissions to the University Hospital of Ceuta they did nothing for him. After the vaccination he had to stop all his basic activities such as playing sports or working, while observing how he became “quadriplegic” as the days passed and suffered a storm of cytokines that the university hospital classified as anxiety. To date, the young man accumulates two hospital admissions in Campo de Gibraltar and in Malaga with dozens of complementary tests and in-depth studies that public health has not been able to carry out to date. He claims not to have received support or help from any public administration so far, “nobody” having been interested in his complicated case that they now classify as “persistent Covid” but not because he has passed Covid, but because he has tried to protect himself against it. The Ministry of Health responded by informing that the direct responsibility corresponds to Ingesa, but at its most critical moment and that it could have cost him his life, they gave him an appointment with the neurologist for 6 months, refusing hospital admission.

Thousands of euros spent to preserve life but that have not prevented cardiac fibrosis that “the cardiologist cannot explain”, a recently discovered mitral valve prolapse, an intolerance to any type of effort that prevents him from even picking up a bag from the purchase and with a very high risk of suffering vascular complications by quintupling the maximum value of the vascular growth factor, among other problems such as lack of concentration, mental fog, digestive and coordination problems along with intense heart pain have motivated the young man to decide file a claim with the Ministry of Health and the Spanish Medicines Agency, but now, after being recognized with a disability of 42% and that does not cover many of his pathologies, he will be forced to go to court, to enforce what considered a fair right.

“The administration does not help you in anything, neither in the health field, nor in the social field. It seems that you have to be begging for something that corresponds to you by law and for which the government should be responsible, having authorized the administration of a product that has not passed all the controls it should. At Ingesa, the only healthcare provider who has cared about me has been the head of internal medicine, but my entire journey in the last year has had to be through private healthcare where they have saved my life, otherwise I would be dead, I am clear” “No studies or investigations are being carried out, since I am not the only one with serious sequelae from these vaccines and who cannot spend a single day of his life without pain or problems. I can’t work, I can’t exert myself and although I have regained much of my mobility, the administration continues to look the other way, as if we didn’t exist. There are other cases like me in Spain and also in Melilla there is a girl of my same age and with my same symptoms and we all feel forgotten by the administration, which seems to be waiting for us to just die. Now I have to take Ingesa to court not only for its negligence with me, but also to have to claim the Form that says that I have not provided enough evidence and the social security that says that I did not present any functional reduction, when there are days that I have trouble even walking.

Thank God I have been able to allow myself deep studies and I have everything documented and with extensive tests: Multiple CT scans, resonances, ultrasounds, admissions, trips, electromyography, electroencephalograms, electroneurography, Holters, stress tests, clinical studies and dozens of cardiologists and Other health workers among the best in Spain have attended me and all this has been provided to both Ingesa and Social Security to Imserso, but it seems that they do not even read the files or do not understand them, since there are analyzes that have cost me up to 400 euros each and that later many doctors have not even been able to interpret; but there are many people who have not been able to afford it and in the end, they have to resign themselves to seeing their lives destroyed from one moment to another and without being able to do anything, I am not going to allow that and that is why I encourage everyone to seek help , because if there is. I have received support from Doctors for the truth, from People Affected by Vaccines, from the Integral Assistance Movement and from the Liberum Association, which put me in contact with a health lawyer, who now handles my entire case, but in short, it is a pity that being victims, on top of that we have to resort to these methods with the administration”.

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