Multielemental analysis of whole blood can provide significant information for the evaluation of nutritional status, diagnosis of certain diseases as well as for the assessment of exposure to potentially toxic metals. However, the quantification of multiple elements in whole blood is not easy partly because of the wide variation in element concentrations (from ng•L-1 to g•L-1) and the complex matrix. The aim of this work was to develop a fast, sustainable and reliable analytical method, in combination with low power TXRF, for multielemental analysis of blood samples. Firstly, a set of experiments were carried out to select the best diluent type and dilution factor using the control material SeronormTM Trace Elements Whole Blood L-1. A critical evaluation of the parameters affecting the sample deposition on the reflector was also carried out including a study of the shape and element distribution of the deposited residue on the reflector by micro X-ray fluorescence spectrometry. Using the best analytical conditions, limits of detection estimated were in the low mg•kg-1 range and similar to those obtained using more complex sample treatments such as digestion. Accuracy and precision of the results were in most cases acceptable (Recoveries: 89-102 %, RSD: 6-8%, n=5). Only underestimated values were obtained for light elements such as potassium. To prove the applicability of the method, several blood samples from control and thyroid diseases patients were analysed. Despite the fact that more samples need to be analysed, it seems that Zn and Br contents in some of the patients are significantly higher compared to control samples.