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  4. RIVULET MEDIA INC. (RIVU) Message Board

At the end of the day, dear man, there are but a h

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Post# of 5066
Posted On: 07/11/2013 8:29:18 AM
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Posted By: patientgal
Re: jayreese #1333

At the end of the day, dear man, there are but a handful of people among the lot of us that would pee on you if you were on fire. The rest could care less about any of us. It is for those like yourself and my belief in the doctors that have worked painstakingly hard to develop these cures & treatments that I submit my dd.


It has been my experience that erroneous and misleading information by way of board postings and blogs can incite fear and panic in the masses who in turn respond in the predictable human way--they run for cover. The share price takes a beating that sometimes may require a good amount of time to recover from unless (until) something monumental occurs.


There are few things more painful than watching your hard work undone by the actions (or inaction's) of the apathetic, ignorant and/or greedy. For whatever the reason this stock has summonsed them all and then some. And they all seem to be determined to capitalize on the spoils of war; delighting in the stench of rotting flesh.


Welcome to the world of 21st century trading I suppose.


It is my philosophy that if you need money, make the money. Consider the rest as a long-term investment that will ultimately see you reaping from it handsomely. At least as far as this stock goes.


As of 7:30 this morning, national and international databases do not reflect the submission of Hemaxellerate for clinical trials initiation. The databases are updated daily though the information is not received and submitted on the same day. If that makes any sense. Nor are there any RSS feeds with a Regen PR (these are updated throughout the day). So, we continue to wait.


If my suspicions are correct based on what I have experienced in my many years of working in this industry, the Q&A should have been pretty simple to complete given the data the treatment already provides. There really is not dialogue with the FDA at this stage--they tell you what they want (what might be missing in your submission or requires clarification) you give it and you go on. Rinse and repeat sometimes.


We are talking about dealing with the United States government. Nothing is ever easy nor as it seems.


Thanks for the Kudos. :-)


BMSN





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