Note 3 Download Software Activation Crack Full Version Trial Reset Interactive Flat Panel Maxhub Benchmark Evota ViewSonic StudynLearn and all other

Title: How to Extend Your Note 3 Interactive Whiteboard Software Trial Period








LOFT | Note 3 Application | Interactive Display | Maxhub Benchmark Evota ViewSonic StudynLearn and all other.


Note 3 is a touchscreen-based interactive whiteboard software designed for education. It works with IWB/IFP and provides whiteboard functions.


Are you using Note 3, the interactive whiteboard software for educational purposes? If so, you might be familiar with the 15-day trial period that comes with it. After this trial period expires, you're required to purchase an activation key, which can cost you anywhere from 3000 to 6000 Rupees, depending on your vendor. But what if there was a way to reset the trial period, allowing you to enjoy the full version with all its Pro features forever? Well, you're in luck because we've got a free trick to help you do just that!








Why Choose Note 3 Interactive Whiteboard Software?

Note 3 is a touchscreen-based interactive whiteboard software designed specifically for education. It's compatible with Interactive Whiteboards (IWBs) and Interactive Flat Panels (IFPs), offering a range of powerful whiteboard functions. Teachers, educators, and students can benefit from its features to enhance their learning and teaching experiences.

Unlocking the Pro Features

To access the full set of features in Note 3, you typically need to purchase an activation key. These Pro features include advanced pens and tools that can significantly improve your interactive whiteboard experience. However, not everyone is keen on spending money for these additional functionalities.

Extend Your Trial Period for Free

Luckily, we have a simple and free trick that will allow you to extend your Note 3 trial period back to 15 days, essentially giving you access to the Pro features indefinitely. Here's how you can do it:

1. Delete all temp and %temp% files using run command.(Ctrl+R)












2. open registry using run. (for Win 11 Users Only) Other users can skip or can check the same .

HKEY_LOCAL_MACHINE\SOFTWARE\WOW6432Node\EasiNote3\SWAF1503

and delete the folder swaf1503. (Windows 11 Only )



3. Open C:\ProgramData\EasiNote3 and delete the swaf1503 file. (Program data is the hidden folder)








That's it. your note 3 will be reset to 15 days trial again.




Enjoy the great Chinese brush.

If this works for you Let me know in the comments.

I'LL update for Note 5 also.
Bye bye



Official Website : https://www.lofttech.com/note
Official Download Link :: Click Here ( Google Drive) - 294MB








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Seedr :Free Torrent Client

I first came across this amazing torrent down-loader accidentally. It’s quite funny that i was looking for seeds (the one used in farming) and happened to tme this “seed”.

I would call this seed since it’s an amazing way all you need is to put the seed (copy-paste the magnetic link) and grows into big and beautiful tree (the downloaded content). I was fed up with all sorts of downloading trouble i was facing as many sites other than seedr offered this service but data was limited and hence i couldn’t download and torrent takes too much time to download the content with less number of seeds and hence this happened to be an amazing life saver to me.

Seedr is a next-generation app aiming to bring the torrent experience to the next level.

Stream movies, music, and books on any device
With top-in-class streaming technology, Seedr allows you to watch movies, listen to music, or read anything in your torrent library directly from the cloud on any device.

Private and safe
Seedr has high-level transport encryption to protect your privacy, and there is no need to worry about malware, viruses, or outside tracking – Seedr is the barrier protecting you.

Very fast
Seedr runs on a high-speed backbone and can fetch torrents to the cloud within several minutes down to several seconds.

If you’ve ever tried using torrents on either tablet or phone, you’d quickly find out how impractical that is . Seedr is the solution – with special mobile-friendly protocols we created a snappy, fast mobile site that has all the functions you get on your PC – including streaming, subtitles and high speed direct downloads.

• We believe that downloading torrents can be friendlier and safer, and plan on expanding the already rich features of the site in the near future.

Overall

Easier to operate than uTorrent (by a long way), Seedr’s beauty lies in its simplicity. It’s hard to imagine anyone other than complete novices needing to revert to the site’s tutorial. However, those that do won’t be disappointed as it reveals ways to integrate the service into Kodi/XBMC.Free tier aside (which is a steal) it’s not cheap at $9.95 per month (two months free on annual rates) so the service might benefit from having a more limited lower-tier premium package around the $6 to $7 mark.

Those who obsess over the minutiae of their torrenting might prefer a full-blown seedbox experience, but Seedr knows its target audience and appears to serve them well.

Seedr can be tested here for free.
https://www.seedr.cc/

Teaching is a Profession , Not Business !!!

Dear Professors, Here’s What Will Make Me Stay In Class, And Not Just For The Attendance !!!

After spending three years completing a bachelor’s degree and a year and a half trying to complete a master’s degree, I realized that frustration has become a second nature to me, and fight or flight, the story of my life. I thought I’ve been PMSing for four years straight, but now I know why. The very attrition and absenteeism that I am studying to curb, is what I indulge in on a very regular basis, because I just cannot seem to stand being in college. I walked into college with the hope of great learning, and learning it was, to expect nothing more than average.

Are you reading this and feeling that this is the story of your life? Do you also dislike going to college with the very same fervour as I do? I feel you my friend. I write to talk about what needs to change in Indian colleges, and fast. Before brain drain becomes a national threat, it’s time that faculty and management paid attention to student feedback and ramped up the grievance redressal system. We are done being the collateral damage of an uptight and antique education system, unwilling to repaint its structures, let alone rebuild.

If only the following four things get implemented, I will become much more than a guest appearance at college.

1. Abolish Compulsory Attendance

This is just a way of keeping students in class. It’s almost a reaffirmation of the fact that if this rule was not in place, hardly anyone would be in class. No comparisons to how universities around the world function, but the 90, 85 and 75 per cent compulsion to be in class is redundant. This is because many times, even though we are sitting in there, we are hardly interested. ‘The attendance rule’ has also become a way of threatening students and tossing superiority by saying that if you come to class five minutes late, your attendance won’t be marked. So does that mean I can walk out?

Colleges should have an attendance bar of 45% and instead of threatening us, they need to consciously work on a way of making class a more interesting place to be in and lectures, a memorable experience. Nothing can stop me from attending a lecture that compels me to think; give your students the gift of curiosity and intellect, not the grind of mediocrity.

2. Stricter Criterion for Professor Recruitment

No disrespect to the people we so ardently call Ma’am/ Sir, but I believe that Universities around the country need to have stricter criteria for Professorship and a more testing recruitment process. I would much love that the people bestowing knowledge upon me at least spoke to me in English instead of making fun of me for not knowing the state language. It seems that our system is willing to settle for mediocrity. It doesn’t matter who is teaching, as long as the material is covered, right? And this usually happens in the form of photo copies and notes dictation that amounts to mugging up and vomiting on the answer sheet.

Professor recruitment needs to be taken up with some strict criterion; for instance- English communicative knowledge, minimum two years of experience in the field, ability to hold attention, presentation skills, holistic subject knowledge, a dynamic teaching plan and interpersonal skills. This is the person who judges my answer sheets and assignments, who gives me scores that dictate my future, who is supposed to set a standard for me; should my professor not be thoroughly tested for his/her holistic competence too? When students are handpicked through aptitude tests and in-depth multi-panel interviews for admission, it is only fair that their faculty members are the cream of the lot too.

3. Paper and Pocket Friendly Education

Not only are we paying a hefty sum as college fees, we are also spending on numerous handwritten assignments taken up as a way to avoid plagiarism. Then there is a multitude of photo-copies and project review copies that we spend on, not to mention the copious amounts of notes we take. One five subject notebook every semester and nearly 1 kg of paper printed for trash. Figuratively speaking, 1 kg per student, 150 students per department, 8 departments in the college and a total of 1200 kgs of paper; where is all this paper going?

Then there are all those answer booklets. Imagine if we could choose to type end semester papers instead of writing them. Laptops would be an investment, alright, but not only would you be standardizing the examination process and increasing our chances of getting better scores, but also preventing the waste of unbelievable amounts of paper.

Allow us to use our cell phones, tablets and laptops to take notes in class; encourage the exchange of information online instead of taking print outs; allow us to submit assignments through email. That way, the pocket money gets saved and the use of paper gets limited; plus, we can stop being judged on our handwriting and start being marked for the quality of our work instead.

4. Challenging Classrooms not Lives 

Many times, being a student is a berating experience, because some of your professors are constantly judging and reprimanding you for being late, for not paying attention, for your handwriting, for the way you dress or even the way you speak. Setting standards is good, but every student is different and as our guides, professors need to respect that. Similarly, respect is earned, not force fed through rules and punishments. Do not set out seeking perfection, set out for growth. Make every class worth talking about even after it’s done, discuss the world with us, ask us about our experiences, involve us in debates about what is right and what is wrong, engage our minds and feed us with a spark for creativity. Encourage us for extempore and discussions, performance based learning and role-play activities; make the classroom a place where we feel like expressing ourselves.

Dear Professors, fortunately for you, this is not just another job. Being a teacher is a paramount responsibility, a responsibility of the future. I am one of those futures, and I refuse to buckle under the pressure to conform; instead I choose to inform you that I want more. Not because I am paying for it, but because I choose to learn and be challenged. It doesn’t even have to be the system, you can change our experience, and just one teacher is all it takes to set the ball rolling. Enter our world and teach us the way we want to learn. We challenge you to challenge us.

[Via: Youth ki awaaz ]

Do Share !!

Know About ALS And Ice Bucket Challenge

What is ALS ?

Amyotrophic lateral sclerosis (ALS), often referred to as "Lou Gehrig's Disease," is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Motor neurons reach from the brain to the spinal cord and from the spinal cord to the muscles throughout the body. The progressive degeneration of the motor neurons in ALS eventually leads to their death. When the motor neurons die, the ability of the brain to initiate and control muscle movement is lost. With voluntary muscle action progressively affected, patients in the later stages of the disease may become totally paralyzed.

A-myo-trophic comes from the Greek language. "A" means no or negative. "Myo" refers to muscle, and "Trophic" means nourishment–"No muscle nourishment." When a muscle has no nourishment, it "atrophies" or wastes away. "Lateral" identifies the areas in a person's spinal cord where portions of the nerve cells that signal and control the muscles are located. As this area degenerates it leads to scarring or hardening ("sclerosis") in the region.

As motor neurons degenerate, they can no longer send impulses to the muscle fibers that normally result in muscle movement. Early symptoms of ALS often include increasing muscle weakness, especially involving the arms and legs, speech, swallowing or breathing. When muscles no longer receive the messages from the motor neurons that they require to function, the muscles begin to atrophy (become smaller). Limbs begin to look "thinner" as muscle tissue atrophies.

More Detail On What Is ALS

Symptoms

At the onset of ALS the symptoms may be so slight that they are frequently overlooked. With regard to the appearance of symptoms and the progression of the illness, the course of the disease may include the following:

• muscle weakness in one or more of the following: hands, arms, legs or the muscles of speech, 
  swallowing or breathing
• twitching (fasciculation) and cramping of muscles, especially those in the hands and feet
• impairment of the use of the arms and legs

• "thick speech" and difficulty in projecting the voice
• in more advanced stages, shortness of breath, difficulty in breathing and swallowing

The initial symptoms of ALS can be quite varied in different people. One person may experience tripping over carpet edges, another person may have trouble lifting and a third person's early symptom may be slurred speech. The rate at which ALS progresses can be quite variable from one person to another. Although the mean survival time with ALS is three to five years, many people live five, ten or more years. In a small number of people, ALS is known to remit or halt its progression, though there is no scientific understanding as to how and why this happens. Symptoms can begin in the muscles of speech, swallowing or in the hands, arms, legs or feet. Not all people with ALS experience the same symptoms or the same sequences or patterns of progression. But, progressive muscle weakness and paralysis are universally experienced.

Muscle weakness is a hallmark initial sign in ALS, occurring in approximately 60% of patients. Early symptoms vary with each individual, but usually include tripping, dropping things, abnormal fatigue of the arms and/or legs, slurred speech, muscle cramps and twitches and/or uncontrollable periods of laughing or crying.

The hands and feet may be affected first, causing difficulty in lifting, walking or using the hands for the activities of daily living such as dressing, washing and buttoning clothes.

As the weakening and paralysis continue to spread to the muscles of the trunk of the body the disease, eventually affects speech, swallowing, chewing and breathing. When the breathing muscles become affected, ultimately, the patient will need permanent ventilatory support in order to survive.

Since ALS attacks only motor neurons, the sense of sight, touch, hearing, taste and smell are not affected. For many people, muscles of the eyes and bladder are generally not affected.

For More Detail On Symptoms

Facts You Should Know About ALS

• ALS is not contagious.

• It is estimated that ALS is responsible for nearly two deaths per hundred thousand population annually.

• Approximately 5,600 people in the U.S. are diagnosed with ALS each year. The incidence of ALS is two per 100,000 people, and it is estimated that as many as 30,000 Americans may have the disease at any given time.

• Although the life expectancy of an ALS patient averages about two to five years from the time of diagnosis, this disease is variable and many people live with quality for five years and more.  More than half of all patients live more than three years after diagnosis.

• About twenty percent of people with ALS live five years or more and up to ten percent will survive more than ten years and five percent will live 20 years. There are people in whom ALS has stopped progressing and a small number of people in whom the symptoms of ALS reversed.

• ALS occurs throughout the world with no racial, ethnic or socioeconomic boundaries.

• ALS can strike anyone.

• The onset of ALS is insidious with muscle weakness or stiffness as early symptoms. Progression of weakness, wasting and paralysis of the muscles of the limbs and trunk as well as those that control vital functions such as speech, swallowing and later breathing generally follows.

Ice Bucket Challenge

The Ice Bucket Challenge, sometimes called the ALS Ice Bucket Challenge, is an activity involving dumping a bucket of ice water on someone's head to promote awareness of the disease amyotrophic lateral sclerosis (ALS) and encourage donations to research. It went viral throughout social media during mid 2014. In the UK, people participate in the challenge for the Motor Neurone Disease Association.

The challenge dares nominated participants to be filmed having a bucket of ice water poured on their heads and challenging others to do the same. A common stipulation is that nominated people have 24 hours to comply or forfeit by way of a charitable financial donation.

 Click Here To Watch My Ice My Ice Bucket Challenge

Rules

Within 24 hours of being challenged, participants have to record a video of themselves in continuous footage. First, they are to announce their acceptance of the challenge followed by pouring ice into a bucket of water. Then, the bucket is to be lifted and poured over the participant's head. Then the participant can call out a challenge to other people.

Whether people choose to donate, perform the challenge, or do both varies. In one version of the challenge, the participant is expected to donate $10 if they have poured the ice water over their head or donate $100 if they have not. In another version, dumping the ice water over the participant's head is done in lieu of any donation, which has led to some criticisms of the challenge being a form of "slacktivism". Individual videos have included the participant saying that they will be making a donation along with performing the challenge.

Click Here For More Info On Ice Bucket Challenge

Note: The Above Material Is Copyright To ALS.org And Wikipedia.

Asif Khan ALS Ice Bucket Challenge || Raise Awareness For ALS

The Ice Bucket Challenge, sometimes called the ALS Ice Bucket Challenge, is an activity involving dumping a bucket of ice water on one's head to promote awareness of the disease amyotrophic lateral sclerosis (ALS) and encourage donations to research. It went viral throughout social media during mid 2014.In the United Kingdom, people also participate in the challenge for the Motor Neurone Disease Association.

The challenge dares nominated participants to be filmed having a bucket of ice water poured on their heads and challenging others to do the same. A common stipulation is that nominated people have 24 hours to comply or forfeit by way of a charitable financial donation.

Raksha Bandhan Special !!

Strangers tying Rakhi - Will you be my brother/sister ?

Tohfa - Raksha Bandhan Special || EmotionaFulls

Genetics Google Group In Developers Way !!