Apps designed to help people find their lost or stolen phones are now being used as spyware by stalkers.

There are dozens of free spyware apps in the Google Play Store and Apple App Store. Some are marketed to anxious parents wanting to track their children or spouses concerned about cheating partners. Others are sold as anti-theft tools to track stolen phones.

In order to get a first-hand look I decided to test one of these apps on myself, and transform my phone into a tracking device for a day.Once I discovered what the app was able to record and track I was given a chilling insight into how easy it would be for a jealous partner or vindictive ex to covertly observe their victim.

Dutch filmmaker Anthony van der Meer used the app to track my every move for a day. Mr van der Meer, who is in Australia to speak at the International Association of Privacy Professionals ANZ summit, made a documentary using a tracking app to trace his stolen phone. In less than a year it was viewed more than 6 million times.I had no idea how easily my phone could be controlled remotely to see, hear and record what I said, everywhere I went and everything I did.

I consented to having the app downloaded and I knew I could be monitored at any time, but I wasn't aware of exactly when I was being watched. And as I went about my usual morning routine, I soon forgot my phone was spying on me.While the app icon was visible on my phone, there is a disguised version available with the innocuous title "system framework". Apart from the icon there were no other signs my phone was compromised.

ABC News has chosen not to name the app used in the experiment, but it is available on the Android app store and is just one of many apps available.

The front and rear cameras, microphone, text messages and phone call logs were able to be remotely accessed.

Using nearby WiFi points and GPS data, my location could be tracked. Where I live, where I work and where I get my morning coffee was all visible.https://www.ttspy.com/remote-spy-phone-app-for-your-employees-to-monitor-their-activities.html

Every smartphone, tablet, and other smart electronic device comes with premium hardware and software features. Because of this, users tend to use their computer less to a point that some ended up not needing computers anymore.

Must Read: For the latest tips, tricks and hacks check out our dedicated section for Android Tricks.

Android devices nowadays can almost do anything that a regular Windows PC can. While smartphones are becoming similar to computers in usability, Android spyware and viruses are becoming more prevalent.

At this point, you may already possess more private information on your phone than you do on your PC. Privacy is one of the biggest issues on smartphones and if you’re wondering whether someone is tracking your phone or spying on your phone, then continue reading.There are many spying apps, and people can easily install them on the phones of other users in order to monitor them.

Understanding what these spying services can do is necessary for detecting spyware and knowing how to get rid of it. In this post, we’ll share with you several tips that can indicate that your phone is being tracked or spied on, and what can be done about it.
Unusual Strange Phone Behavior

One of the most common ways to detect spyware is to check for odd or strange behavior from your phone. If there is spyware or tracking software installed on your phone, chances are, your phone will act differently.
Unusual Battery Drain

Another useful way to find out whether someone is spying on your phone is an increase in battery usage. After using a phone for a couple of weeks, most people become familiar with battery patterns and know their average battery life. If your phone is suddenly experiencing sub-par battery life for no tangible reason, it could be spyware. Spyware and tracking apps can drain your phone’s battery, especially if they’re running constantly.
Noise During Phone Calls

Look for unusual noise or sounds during phone calls. If you hear beeps or any other sounds during phone calls, then this can mean your calls are being recorded. Call recording apps can make such noises.

Also, if the call quality has suddenly worsened, this can also mean that your phone calls are being recorded. Static or feedback can be signs. However, it might also mean that you simply have a bad connection or that your phone isn’t handling calls well. The world isn’t always a sinister place; but its parts, including carriers and cell phones, have no shortage of problems.https://www.ttspy.com/remote-spy-phone-app-for-your-employees-to-monitor-their-activities.html

NSI-189 Dosage: Neuralstem, Inc. is currently running clinical trials for its use in major depressive disorder, in addition to treating cognitive impairments, and brain degeneration. NSI-189 stimulates neurogenesis of the human hippocampus. NSI-189 dosage was 40 mg-80 mg daily for 12 weeks.NSi-189 powder
NSI-189 increases sociability interactions while enhancing confidence and improved life decisions that lead to elevated sexual enjoyment and quality of life.

NSI-189 review

NSI-189 stimulates neurogenesis of the human hippocampus.

Modern antidepressants focus on the monoamine neurotransmitter system. However, 66% of people treated for major depression disorder achieve clinically significant improvements.

Current antidepressants have long term side effects with negative consequences. Neuralstem Inc proposes that NSI-189 uses different pathways.

NSI-189 Benefits

Ability to control emotions that continue after cessation
Being fluent in speaking and writing.
Improved memory energy
Sharpness of vision
Logical and emotional difficulties resolve
Increased sexual enjoyment and quality of life.
Sociability and interactions are maintained with ease
Confidence while enhancing confidence and improved life decisions.
Reports indicate that suicidal tendencies disappear and personal relationships improve with a broad spectrum of reporting.

PROPIONYL-L-CARNITINE

Propionyl-L-carnitine is a chemical. It is made in the body. Propionyl-L-carnitine is related to two other compounds called L-carnitine and acetyl-L-carnitine.

Propionyl-L-carnitine is commonly used for treating leg pain (intermittent claudication) due to poor blood circulation (peripheral vascular disease, PVD). PVD is often caused by diabetes or “hardening of the arteries” (atherosclerosis). Propionyl-L-carnitine is also used to treat congestive heart failure (CHF), chest pain (angina), and some bowel problems such as ulcerative colitis. A specific kind of propionyl-L-carnitine, called glycine propionyl-L-carnitine, is often used to improve athletic ability. There is limited scientific research that supports taking propionyl-L-carnitine by mouth for other uses..Glycine Propionyl-L-Carnitine powder

Healthcare providers may give propionyl-L-carnitine with a needle into the vein (by IV) for treating PVD and intermittent claudication; to improve wound healing in people with PVD; and to treat heart disease, including congestive heart failure, and chest pain (angina).

How does it work?
Propionyl-L-carnitine helps the body produce energy. It is important for heart function, muscle movement, and many other body processes. It also seems to help increase circulation.

FLADRAFINIL BUY (CRL 40 941) 1000 MG

Eugeroics are a well-documented family that improves brain function by preventing the reuptake of dopamine.CRL-40,941 powder

A Fladrafinil dose is similar to

Adrafinil
Hydrafinil
Flmodafinil
CE-123
Modafinil
Eugeroics are well-documented tools for shift workers that have issues with daytime sleepiness and the preferred choice of nootropics for many CEO according to the surveys.

highly anti-aggressive properties

Fladrafinil is a bis(p-fluoro) ring-substituted derivative of adrafinil that requires the first pass through the liver and is eventually metabolized into Modafinil.

Adrafinil and Modafinil are tremendously powerful chemicals made popular because they substantially increasing focus memory and cognition.

Tryptamines and beta-carbolines are two classes of psychoactive indoles found in plants and animals (1). They have been implicated in a host of neurological functions and display a wide range of neurological activity, which is dependent on their molecular configurations (2). A subgroup of (beta)-carbolines found in some plants are known as the harmala alkaloids; e.g. harmaline in Peganum harmala or Banisteriopsis caapi. Some beta-carbolines have been detected in the tissues and fluids of mammals, including humans, where they are thought to be produced from endogenous tryptamines such as serotonin, 5-methoxy-tryptamine and tryptamine itself. Psychoactive methylated tryptamines such as dimethyltryptamine (DMT), 5-methoxy-dimethyltryptamine (5-MeO-DMT) and 5-hydroxy-dimethyltryptamine (bufotenine) and have been detected in normal human beings as well (3,4,5), though their biological purpose remains a mystery.beta carboline

The psychoactive indoles are interesting not only for their exogenously induced effects on the human mind, but also for their natural occurrence in humans. In the early 1950's, Osmond and Smythies, in their transmethylation hypothesis, proposed endogenous 'schizotoxins' to be responsible for the symptoms characteristic of hallucinatory psychoses, and initiated an era of search for the chemical basis of undesirable states of mind (6). This search was later confounded by the fact that these substances were also found in otherwise normal humans, in addition to many of the other animals in the scientific barnyard. At that time, the psychedelics were commonly referred to as 'psychotomimetics' and 'models for psychosis', and it was difficult to rationalize a normal function for an endogenous psychedelic. Unfortunately, the idea of normal dreaming did not occur to the early pioneers as a possible function for the natural occurrence of endogenous psychedelic substances (7,8).

The Tryptamines Serotonin, melatonin, bufotenine, DMT, 5-MeO-DMT, and tryptamine are well known examples of this group. They primarily originate from tryptophan, an essential amino acid obtained through the diet. All of these tryptamines interact within the central nervous system. DMT is a very potent psychedelic chemical when smoked or injected, but is orally inactive. The onset of its effects are known to be extremely fast, brief and intense. One could say that DMT evokes a transient psychedelic test pattern, exploding with color imagery. 5-MeO-DMT shares similar properties, but is often devoid of visual imagery at effective doses. Its effects have been described as primarily emotive. Bufotenine shares similar properties with these two, especially in terms of a fast onset and short duration of intense action. However, at effective doses, any psychoactivity of interest is essentially lost in the physiological noise it elicits through the serotonergic system. Early reports on the effects of bufotenine in humans clearly indicate its psychoactivity (9), though its polar quality apparently hinders significant passage into the brain. Perhaps the psychoactivity of bufotenine is actually due to its enzymatic conversion to 5-MeO-DMT.

Centrophenoxine is synthesized from DMAE. DMAE is a natural chemical that has been shown to improve areas of cognition and mood. DMAE’s exact method of action is slightly disputed. Some see it as a precursor to Acetylcholine but others contest this as choline molecules broken down from DMAE are not believed to cross the blood-brain-barrier efficiently.DMAE vs. CentrophenoxineIt is not clear how the method of action differs from DMAE to Centrophenoxine. One thing for sure is that Centrophenoxine is much stronger than DMAE as a nootropic. This is likely due to a higher bioavailability of Centrophenoxine or a difference in how it is metabolized in the liver. If you are taking DMAE as a choline source, consider switching to Centrophenoxine as it is known to be more powerful as a nootropic substance.Both substances are broken down in the liver. The liver metabolizes both substances and breaks them down into choline or phospholipid molecules.Centrophenoxine
DMAE has been suggested to have limited effectiveness because the choline molecules are charged and therefore have limited effectiveness in getting to the brain.Centrophenoxine Method of ActionCholine and certain phospholipids are converted into Acetylcholine. Acetylcholine is important and higher levels and receptor uptake will lead to better cognition. Not all choline will be converted into Acetylcholine and there are several processes that take place between the choline to Acetylcholine conversation. It seems as not all choline sources are created equal. Some sources will have much higher levels of Acetylcholine conversion.Centrophenoxine’s primary method of action is believed to be caused by increased levels of Acetylcholine. Whether this is from breakdown into choline or related phospholipids’ is unclear. There are several phospholipids that will also convert into Acetylcholine. This may be an area where Centrophenoxine is more superior to DMAE.
With this said, the general consensus is that Centrophenoxine supplementation leads to higher Acetylcholine levels and better cognition.Centrophenoxine also may have effects on other neurotransmitters in the brain. It has been suggested to help with mood.Claimed BenefitsCentrophenoxine has been marketed under trade names such as “Lucidril” in some countries. In medical science, Centrophenoxine has been tested for use in treating several cognitive disorders.Centrophenoxine is also an excellent antioxidant. It helps to reduce free radicals in the brain. It is more superior to DMAE as an antioxidant. For this reason, Centrophenoxine has been promoted to reduce “brain aging” and is marketed primarily as a powerful antioxidant.Side EffectsCentrophenoxine has been seen to be well tolerated.
Although this is true, side effects can still occur. These side effects are more likely in higher doses and when combined with other substances. If you are on prescription drugs you should speak with your doctor to assist in avoiding interactions with Centrophenoxine. Below are some common side effects of Centrophenoxine.HeadacheNauseaDizzinessGastronintesinal issuesJaw clenchingIrritabilityIf you do experience side effects it is recommended to discontinue use and speak to a doctor.Centrophenoxine vs. Alpha GPC vs. CDP CholineCentrophenoxine, like Alpha GPC and CDP Choline is an excellent Acetylcholine source. Comparing the three is very hard as it comes down to personal experimentation to find the best supplement for you. If you are using nootropics like racetams, an Acetylcholine source will often be added to potentiate effects. Centrophenoxine, Alpha GPC or CDP Choline may all be options for you. These three options are the best choices for choline supplementation.

Coluracetam is a nootropic in the racetam family. It shares the same 2-pyrrolidone base structure as all racetams. Coluracetam differs from the structure of piracetam by the addition of a bulky dimethyl-tetrahydrofuro-quinolinyl grouping. It has a molar mass of 341.404 g/mol and a molecular formula of C19H23N3O3.Coluracetam

CAS: 135463-81-9

IUPAC: N-(2,3-Dimethyl-5,6,7,8-tetrahydrofuro[2,3-b]quinolin-4-yl)-2-(2-oxo-1-pyrrolidinyl)acetamide

Product contains one jar of Coluracetam, in either .5g, 1g or 5g amounts.

Attention: All chemical compounds have risks. Please read the available research and understand the associated risks before handling. If you are uncertain of the appropriate handling methods, please consult a qualified professional. Misuse of this product may result in adverse reactions. This product is not approved by the FDA.
Ingredients: Coluracetam [2-(2-oxopyrrolidin-1-yl)-N-(2,3-dimethyl-5,6,7,8-tetrahydrofuro2,3-b quinolin-4-yl)acetoamide].

Ship code/Instructions: Ambient temperature only.

Storage Instructions: Coluracetam should not be refrigerated. Store at room temperature only.

Dosage Instructions: Coluracetam is known to be a somewhat fast-acting nootropic. It has been noted that neural tissues can detect it within 30 minutes of ingestion. The suggested dosage for Coluracetam is 48-480mcg/kg. For example, a person weighing 70kg should take between 3 and 33mg.

The Coluracetam nootropic stacks well with choline and the two are often taken together. The combination is used frequently for added memory and cognitive ability benefits. Those taking both Coluracetam and choline should take 300mg to 600mg of choline daily (if you are taking Alpha GPC) and 250mg to 750mg daily if using CDP Choline.

There is little information currently available on the toxicity of Coluracetam. Doses given at the above increments demonstrated no negative side-effects.

Side-effects: First time users of nootropics may develop headaches after use. This is common for people who have not used nootropics before. There is no reason for concern. When taking both Coluracetam and choline together, the risk of headaches will be reduced.

ATTENTION: This compound should be used for research purposes only. All chemical compounds have risks. Please consult your physician and understand the available research before consumption. This product is not intended to diagnose, treat, cure, or prevent any disease.

Flmodafinil is the most potent legal eurogic known to man, it is a closely related smart drug to Modafinil Adrafinil, Fladrafinil, and Hydrafinil.Modafinil is a popular wakefulness drug prescribed to many CEO types of fortune 500 companies. CRL-40,940 powder

Yes, Flmodafinil capsules are legal to buy for research purposes only.Modafinil, Adrafinil, Hydrafinil, Fladrafinil (CRL-40,941) and Flmodafinil (CRL-40,940), come from the French "Laboratories Laflon".

Dr. Michel Jouvet uncovered these eurogics in the 1970s.Laflon Lab scientists made a crucial observation in their patent applications.

"In man, particularly old people, it was observed that ... CRL-40,940 ... administered in the form of gel capsules or tablets – each containing 100 to 200 mg of the active ingredient, at the rate of 1 to 3 capsules as arousing medicaments.Flmodafinil dosage in clinical studies was in the range of 100 mg to 600 mg Daily. It is considered safer than caffeine and lacks addictive properties.

In 2015 a new patent was filed under a new name Lauflumide a derivative of modafinil.(2-((bis(4-fluorophenyl)methane)sulfinyl)acetamide) Lauflumide is more effective than adrafinil or modafinil with fewer side effects. It was made very clear in the application that CRL-40,940 lacks any resemblance to amphetamines in effect or structure.

Department of Histology and Embryology, Medical Academy, Lithuanian University of Health Sciences, Kaunas, LT 44307, Lithuania
2Institute of Cardiology of Lithuanian University of Health Sciences, Kaunas, LT 50009, Lithuania
3Laboratory of Molecular Oncology, National Cancer Institute, LT 08660 Vilnius, Lithuania
4Biological Research Center, Lithuanian University of Health Sciences, Kaunas, LT 47181, Lithuania

Received 24 July 2018; Revised 26 February 2019; Accepted 8 April 2019; Published 24 April 2019

Copyright © 2019 Jūratė Stanevičiūtė et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.Testosterone Dichloroacetate
The aim was to investigate the effect of dichloroacetate (DCA) on thymus weight, Hassall’s corpuscle number (HCs), and NKCC1 RNA expression in Wistar rats aged 4–5 weeks. They were investigated in the controls and DCA-treated gonad-intact and castrated males and females. The treatment lasted 4 weeks with DCA 200 mg/kg/day. At the end of the experiment, rat thymus was weighted, and its lobe was taken for the expression of NKCC1 RNA determined by the PCR method and of Hassall’s corpuscles by immunohistochemistry. DCA caused a thymus weight decrease in DCA-treated gonad-intact rats of both genders as compared with their controls (p < 0.05), and no such impact was found in castrated DCA-treated males and females. DCA caused an increase of the HCs in gonad-intact males (p < 0.05), and no such increase in the DCA-treated gonad-intact females was found. There was gender-related difference in the HCs when comparing DCA-treated gonad-intact males and females: males showed significantly higher HCs (p < 0.05); no gender-related differences were found in the castrated DCA-treated groups. The Slc12a2 gene RNA expression level was found to be significantly decreased only in gonad-intact and in castrated DCA-treated males. The authors discuss the gender-related DCA effects on the thymus.