Pulses and strokes will keep you hard and on the edge almost permanently. Ramp up the volume on this estim sound file and can you last until the end? We recommend an electrode below the balls (B), and an electrode on the glans penis (A). It also works well TriPhase with a common as a cock ring and B on the prostate. Alternatively, this track is excellent with a PES Big Jim on A and B.
Imagine long-limbed limber fingered aliens have abducted you and taken control of your sexual organs. This track will take you to outer space and beyond with a wide variation of pleasurable and slightly stinging sensations. Use Ch A on the cock or Clitoris and Ch B in the anus. An out of this world estim sound file.
Estim Wav Filesl
This list of downloadable estim / electrosex, electrostim wav / mp3 files by Dr Orgasm was last updated on Jul 26, 2021 @ 5:05 am. Further update. Dr Orgasm has been working on more brand new, original, earth-shattering orgasmic sound files ready for upload once the COVID lockdown is lifted.
Encoding as 8 kHz single-ch MPEG-2.5 Layer III VBR(q=0)Frame CPU time/estim REAL time/estim play/CPU ETA27237/27237 (100%) 0:12/ 0:12 0:12/ 0:12 155.89x 0:0064 [27237] ***************************************************************----------------------------------------------kbps mono % long switch short %64.0 100.0 84.1 8.9 7.0If you want to save my convertion quickly for a later, download my Convert WAV to mp3 from a directory with lame shell script here
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In a Cochrane review, Mulvey et al (2010) evaluated the analgesic effectiveness of TENS for the treatment of phantom pain and stump pain following amputation in adults. These investigators searched MEDLINE, Cochrane Central Register of Controlled Trials (CENTRAL), EMBASE, PsycINFO, AMED, CINAHL, PEDRO and SPORTDiscus (February 2010). Only randomized controlled trials (RCTs) investigating the use of TENS for the management of phantom pain and stump pain following an amputation in adults were included. Two review authors independently assessed trial quality and extracted data. It was planned that where available and appropriate, data from outcome measures were to be pooled and presented as an overall estimate of the effectiveness of TENS. No RCTs that examined the effectiveness of TENS for the treatment of phantom pain and stump pain in adults were identified by the searches. The authors concluded that there were no RCTs on which to judge the effectiveness of TENS for the management of phantom pain and stump pain. The published literature on TENS for phantom pain and stump pain lacks the methodological rigor and robust reporting needed to confidently assess its effectiveness. They stated that further RCT evidence is needed before such a judgment can be made.
Zeng et al (2015) examined the effectiveness of different electrical stimulation (ES) therapies in pain relief of patients with knee osteoarthritis (OA). Electronic databases including MEDLINE, Embase and Cochrane Library were searched through for RCTs comparing any ES therapies with control interventions (sham or blank) or with each other. Bayesian network meta-analysis was used to combine both the direct and indirect evidence on treatment effectiveness. A total of 27 trials and 6 types of ES therapies, including high-frequency TENS (h-TENS), low-frequency TENS (l-TENS), neuromuscular electrical stimulation (NMES), interferential current (IFC), pulsed electrical stimulation (PES), and noninvasive interactive neurostimulation (NIN), were included. Interferential current is the only significantly effective treatment in terms of both pain intensity and change pain score at last follow-up time-point when compared with the control group. Meanwhile, IFC showed the greatest probability of being the best option among the 6 treatment methods in pain relief. These estimates barely changed in sensitivity analysis. However, the evidence of heterogeneity and the limitation in sample size of some studies could be a potential threat to the validity of results. The authors conclude that IFC seems to be the most promising pain relief treatment for the management of knee OA. However, evidence was limited due to the heterogeneity and small number of included trials. Although the recommendation level of the other ES therapies is either uncertain (h-TENS) or not appropriate (l-TENS, NMES, PES and NIN) for pain relief, it is likely that none of the interventions is dangerous.
Aliyev and Geiger (2012) examined the effects of cell-stimulation therapy of lateral epicondylitis with frequency-modulated low-intensity electric current. Patients with lateral epicondylitis were subjected to a 12-week cell-stimulation therapy with low-intensity frequency-modulated electric current in addition to routine therapy. Patients in the control group received the same routine therapy and sham stimulation (the therapeutic apparatus was not energized). The effectiveness of MPS was estimated by comparing medical indices before therapy and at the end of a 12-week therapeutic course using a 10-point pain severity numeric rating scale (NRS) and Roles-Maudsley pain score. The study revealed high therapeutic efficiency of cell-stimulation with low-intensity electric current resulting probably from up-regulation of intracellular transmitters, interleukins, and prostaglandins playing the key role in the regulation of inflammation. The findings of this study need to be validated by well-designed studies with long-term follow-up.
Dabby and associates (2018) stated that peripheral neuropathic pain (PNP) is caused by neuronal damage to the peripheral nervous system (PNS) and usually affects the distal extremities. In an open-label study, these researchers examined the effect of short-term PNS on individuals with PNP due to polyneuropathy. A total of 12 patients (mean age of 63.0 10.0 years, 41.7 % men) with daily bilateral PNP for at least 6 months (mean duration of neuropathic pain of 7.4 7.8 years) received a total of 6 direct electrical stimulation therapies to the posterior tibial nerve at 3 to 4-day intervals; 8 patients completed the study and were included in the efficacy analysis. The average pain at baseline was 36.6 3.80 estimated by the Short-Form McGill Pain Questionnaire. After the last stimulation, pain was significantly reduced by 85.5 % to 4.88 3.1 (p = 0.008); 6 patients (75 %) had over 50 % decrease in pain after the first stimulation therapy and 99.2 % after the final stimulation therapy. The patients also reported statistically significant decreases in pain level (measured by VAS), ranging from 54.85 % to 87.50 % after each of the stimulations as compared to the pain experienced prior to the stimulations. The authors concluded that the procedure was safe without any serious AEs; PNS has shown excellent efficacy and improvement of PNP symptoms. Moreover, they stated that further studies in larger patient populations and longer duration are needed.
Kovacic et al (2017) stated that development of safe and effective therapies for pediatric abdominal pain-related functional gastro-intestinal (GI) disorders is needed. A non-invasive, Food and Drug Administration (FDA)-cleared device (Neuro-Stim, Innovative Health Solutions, IN, USA) delivers PENFS in the external ear to modulate central pain pathways. In randomized, double-blind, sham-controlled trial, these researchers examined the efficacy of PENFS in adolescents with abdominal pain-related functional GI disorders. They enrolled adolescents (aged 11 to 18 years) who met Rome III criteria for abdominal pain-related functional GI disorders from a single U.S. outpatient gastroenterology clinic. Patients were randomly assigned (1:1) with a computer-generated randomization scheme to active treatment or sham (no electrical charge) for 4 weeks. Patients were stratified by sex and presence or absence of nausea. Allocation was concealed from participants, caregivers, and the research team. The primary efficacy endpoint was change in abdominal pain scores. These investigators measured improvement in worst abdominal pain and composite pain score using the Pain Frequency-Severity-Duration (PFSD) scale. Participants with less than 1 week of data and those with organic disease identified after enrolment were excluded from the modified intention-to-treat (ITT) population. Between June 18, 2015 and November 17, 2016, a total of 115 children with abdominal pain-related functional GI disorders were enrolled and assigned to either PENFS (n = 60) with an active device or sham (n = 55). After exclusion of patients who discontinued treatment (n = 1 in the PENFS group; n = 7 in the sham group) and those who were excluded after randomization because they had organic disease (n = 2 in the PENFS group; n = 1 in the sham group), 57 patients in the PENFS group and 47 patients in the sham group were included in the primary analysis. Patients in the PENFS group had greater reduction in worst pain compared with sham after 3 weeks of treatment (PENFS: median score 5.0 [inter-quartile range [IQR] 4.0 to 7.0]; sham: 7.0 [5.0 to 9.0]; least square means estimate of change in worse pain 2.15 [95 % CI: 1.37 to 2.93], p 2ff7e9595c
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