Patients feel they are being treated like malingerers
Patients who can prove with medical certificates that they are not mobile regularly complain. Nevertheless, they are expected to travel to an examination centre. "I expect the PVA, but above all the Ministry of Social Affairs Service SMS, to provide better training for the assessors. But it's also about the fundamental approach: The assessors could give more credence to the patients and the findings. However, many feel they are being treated as potential malingerers."
"Patients who are not mobile should be assessed at home. If they have to make the extra journey to assessment centres, there is a risk of massive deterioration in their health," says Achitz: "Time and again, insurance providers and authorities accommodate those patients who have turned to the Ombudsman Board. This is very welcome, but not enough," says Achitz: "I appeal to the PVA, but also to other public authorities, to make home visits to ME/CFS sufferers the standard for patients who cannot be transported - even in cases where no one has contacted the Ombudsman Board."
Social security
ME/CFS sufferers also frequently turn to the Ombudsman Board because they encounter major obstacles to their social security. In most cases, the pension insurance (PVA) is responsible for both the care allowance and the rehabilitation allowance or disability pension. The Ombudsman Board has been able to successfully intervene in some cases where, for example, medical findings were not taken into account and claims were therefore rejected.
Patients who have lost their health insurance cover also turn to the Ombudsman Board. This mainly affects people who have been "taxed out" of health insurance (entitlement to sickness benefit has been exhausted) and do not (yet) receive any other benefits (e.g. rehab money), but are unable to work due to their state of health. "They usually have to make sure they remain insured themselves," says Achitz.
Ombudsman Achitz: Patients who are not mobile should be assessed at home.
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