Combining therapies for an even faster and more effective resolution of specific pathologies: ASA has developed its therapeutic solutions to this end, and when correctly combined, they have proven to be particularly valuable in accelerating recovery times.
Hilterapia®, MLS® Laser Therapy, and Magnetotherapy are therefore strategic in enhancing the performance of the doctors and physiotherapists who use them and, in parallel, in increasing the satisfaction of the patients, who can regain their best physical condition in few sessions.
This is confirmed by Francisco Màrquez (Operations Director and co-founder of INNERGY Fisioterapia Avanzada y Osteopatia, Mexico), who works with MLS® and Magnetotherapy on a daily basis.
ASA’s MLS® Laser Therapy and Magnetotherapy are therapies that you often adopt in the therapeutic plan designed for the patients who come to you. What are their strengths?
Their value is twofold and concerns both the method of application and the effectiveness of the results, linked to the maximum quality of the therapies. From a methodological point of view, I refer specifically to the global approach, which, by promoting the treatment of the area of the pathology and the areas connected to it at the same time, reduces pain from the very first session, favouring full recovery in a short amount of time. Being able to treat the root of the pathology and the symptoms that derive from it leads to considerable results, achievable thanks to the value of the therapeutic solutions. MLS® Laser Therapy, for example, by allowing me to penetrate the joint tissues in depth, offers excellent physiological effects.
I feel more complete, not only because I offer my patients highly innovative therapies, but also because I have been able to acquire additional skills. ASA does not just provide the devices, but also all the essential information to make the best of them.
Regarding your day-to-day work experience, in the treatment of which pathologies did MLS® Laser Therapy and Magnetotherapy allow you to achieve the objective of well-being that you had set for the patients?
Magnetotherapy has given me excellent results especially in the treatment of bone fractures, accelerating the consolidation times, while MLS® has confirmed its effectiveness in the post-operative phase of patients subjected, for example, to arthroscopies and joint prostheses as well as in muscle-tendon injuries. The patients themselves realize this, noticing how much less time it takes for the cells to repair and, consequently, for the lesions to heal.
When it comes to recovering, can the joint use of the two therapies also be valid?
Yes. I had the opportunity to use Magnetotherapy and MLS® Laser Therapy together for some pathologies and the results were very positive, starting from the reduction of symptoms. The feedback comes from the patients themselves who, satisfied with feeling better, become a channel of resonance for the therapies, recommending them.
The positive word of mouth of the patients must have certainly affected your work. Do you think that your profession has benefited from adopting ASA’s therapies?
Undoubtedly. I feel more complete, not only because I offer my patients highly innovative therapies that have concrete results, but also because I have been able to acquire additional skills that have complemented what I studied and then verified with experience. The more distinctly ‘educational’ component that the company offers should not, in fact, be underestimated. ASA does not just provide the devices, but also all the essential information to make the best of them. Last but not least, the ease of use of the devices, with user-friendly software and very detailed protocols, also makes the application of the therapy much easier.
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Decreto Legislativo 24 febbraio 1997, n°46 Articolo 21
1. E' vietata la pubblicità verso il pubblico dei dispositivi che, secondo disposizioni adottate con decreto del Ministro della Sanità, possono essere venduti soltanto su prescrizione medica o essere impiegati eventualmente con l'assistenza di un medico o di altro professionista sanitario.
2. La pubblicità presso il pubblico dei dispositivi diversi da quelli di cui al comma 1 è soggetta ad autorizzazione del Ministero della Sanità. Sulle domande di autorizzazione esprime parere la Commissione di esperti prevista dall'articolo 6, comma 3, del decreto legislativo
30 dicembre 1992, n. 541, che a tal fine è integrata da un rappresentante del Dipartimento del Ministero della Sanità competente in materia di dispositivi medici e da uno del Ministero dell'Industria, del commercio e dell'artigianato.
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