Six-Year-old girl gives her just got divorced mother a lesson in love and friendship.

The best out of the mouths of babes. Bright beyond her 6 years in this video.

Maine Republic Email Alert

View original post

All Ducks in a Row’….. Be Alarmed!!!

David Robinson has some intriguing posts on his blog. This one is eye-opening and scary. I had no idea that so many of our top military and naval commanders were relieved of duty in one way or another. IMO this does not bode well for our security.

Maine Republic Email Alert

When you see the number of high ranking military officials who have been fired or just let go it IS SCARY!   When I checked out the internet to see how many current Muslims are in the White House it covered 26 pages. Most people ARE COMPLETELY UNAWARE of what is happening to our country!!!
The picture below is of the five first line US nuclear carriers docked together in one place. Just like Battleship Row, Pearl Harbor, December 7, 1941.
This picture was taken the February 2014 in Norfolk, Virginia. Obama ordered 5 nuclear carriers into harbor for “routine” (?) inspections. Heads of the Navy were flabbergasted by the directive but had to comply as it was a direct order from their Commander-in-Chief.
These carriers were all pulled out from the MIDDLE EAST and the Afghanistan support role leaving our land forces naked and exposed without the air support needed…

View original post 1,898 more words

Why Is Big Pharma Fighting Legalizing Marijuana?

 

MJ

It’s obvious.

We all know by now that most prescribed pain killers (especially opioids) are addictive, and yet, our government bows down to Big Pharma and continues to allow clinicians to prescribe them indiscriminately.

Many, many committees, commissions, agencies , etc., have been holding meetings to discuss this problem.  Has anything been done?  Of course not.

All the “conclusions” of these “get-togethers” have amounted to: ZERO.

Now, we have something else to throw into the “pot.”

There’s a body of research showing that painkiller abuse and overdose are lower in states with medical marijuana laws. These studies have generally assumed that when medical marijuana is available, pain patients are increasingly choosing pot over powerful and deadly prescription narcotics. But that’s always been just an assumption.

Now a new study, released in the journal Health Affairs, validates these findings by providing clear evidence of a missing link in the causal chain running from medical marijuana to falling overdoses. Ashley and W. David Bradford, a daughter-father pair of researchers at the University of Georgia, scoured the database of all prescription drugs paid for under Medicare Part D from 2010 to 2013.

Medical marijuana is being used for medicinal purposes and not for “recreational” purposes.  There is this misconception held by very conservative groups:  medical marijuana will be used for recreational purposes or will lead to recreational marijuana use in order to get “high.”  Medical marijuana is used as medicine to relieve pain and other symptoms of chronic and/or serious medical conditions.

fewer pills

The graph above, published by Bradford and Bradford, Health Affairs, July 2016, sheds much light on the impact the use of medical marijuana has had and continues to have, on addictive drug use.

Let’s get on with it, elected officials!  Let the light shine through, and give our ill citizens availability to this plant that has many healing qualities, especially relief from many types of pain.  Some of your colleagues have seen the light and passed state laws allowing prescribing of medical marijuana.  Until the federal government passes a national law or properly amends the scheduling of marijuana, I hope more states will join the almost 30 states which have already passed marijuana laws.

Source:  Article in the The Washington Post by Christopher Ingraham

[ Header image from http://www.freewebheaders.com ]

 

Rainbow Over Lake Michigan!

I wonder if this is the one with the pot of gold at the end?

The Chicago Files

Rainbow 3

Oh what an absolute delight to see a rainbow over Lake Michigan, on a midsummer’s night!

View original post

One of #MillionsMissing

My daughter has ME – Myalgic Encephalomyelitis.  She’s one of those “#Millions Missing.”  On May 25th of this year, there was a world-wide campaign during which millions of pairs of shoes were placed in front of government buildings to show support for the millions of patients who are “missing” from participating in a “normal” life.  A life which they, against their wishes, were forced to leave, due to the debilitating nature of this horrible disease.

There is no known scientific diagnosis; no cure; and no recognized treatment.  Expert clinicians are still experimenting with medications, supplements, etc., while trying to find ways in which to help their patients.  Some things work – but not for long – to help relieve symptoms.  Each patient reacts differently to these “experiments.”  No such thing as “one size fits all.”

My daughter’s symptoms started approximately 25 years ago.  It was not a sudden onset like many other patients.

It occurred slowly over these many years.  The last two years were the worst.  She was still working, but truthfully, towards the end of 2014, I was positive she couldn’t continue with her job.  I don’t know how she did it, and looking back, she doesn’t, either.

She sort of set goals for herself.  Just another month, just another week.  She finally gave it up at the beginning of this January, when her body just gave up.

She cut her hair years ago.  She didn’t have the strength to take care of it anymore.  She used to have such beautiful, long hair.

There were many other activities of daily living (ADLs) she had to stop.  Frugally managing her time and energy allowed her to hold on for another year at the work site.

It wasn’t only the profound exhaustion.  There is the pain – in every part of her body.  She has told me that even her hair feels pain during the worst days.  The viral outbreaks.  The painful and debilitating chronic migraines which could last for days and keep her in bed, immobilized.  Did you ever hear of a migraine in the optic nerve?  Now, I have.

The “brain fog” and the constant wanting to put her head down and sleep.  Concentration was non-existent.  All these symptoms, put together as they were, forced her to bed.  Work was out of the question.  And she suffered all these and more, while trying so hard to keep her job and not appear to be sick at the office.  They frowned upon “being sick.”

She spends most of her days either lying on the couch or in bed.  It’s not where she would like to be.  She is forced to give up a “normal” life.

Talking on the phone is exhausting, and many is the time I’ve told her to hang up because I can hear and feel the extreme effort in her voice as it slows and gets slurry.

ME patients ARE NOT LAZY; THEY ARE NOT MALINGERERS.  Too many patients have lost their families and friends and even doctors.  These people refuse to believe the patient is REALLY SICK and they crossed the patients off their “list.”  They walked away.  That may be the most debilitating and greatest loss of all.

I’ve touched on only a very small amount of her symptoms.  The general public will find it impossible to understand that which patients go through in trying to manage from day to day; hour to hour.

Each day is different.  She never can expect that the next day will be better.  Too many times, it is worse.  There really is no such thing as “better.”  Sometimes she knows she has over-spent whatever energy (spoons) she had on the day before, and her body lets her know about it, for sure, during the next few days at least.

Myalgic Encephalomyelitis is a multi-symptom chronic disease.  All patients do not suffer in the exact same way; however, they do share most of the known symptoms.  As I said above, “each day is different” for each patient.

Sweetheart, if you are reading this, remember I love you so very much.  Words are not enough.  You know.  It is there in the depths of my being.

This post is my ode to you.  You are the most inspiring person I’ve ever known.  And you happen to be my daughter!:-)

 

[ Header image from http://www.freewebheaders.com ]

Are You Happy With The Status Quo?

 

I’m not.  This is my first (and maybe the only) post about the upcoming election.

Bernie

I changed my party affiliation from Independent to Democrat only because I wanted to vote for Bernie in the primary.  It was a decision that I did not make lightly:  I felt strongly that Hillary was not the one I wanted to represent me during the next four presidential years.

bernie 2I firmly believed (and still do) that our country needed a change – not the one that Barack promised and was not able to deliver – but a REAL CHANGE.  A change that encompassed all of our societal strata.

bernie 4Just because Bernie did not win the primary, does not mean his supporters will throw up their hands in defeat and turn away.  His supporters are as strong as ever, and for the most part, will not vote for the presumptive nominee(s).

bernie 7It was said somewhere at some time, that Bernie was “not the politician for the job.”  And, that someone who wants to run for the presidential office needs leverage.

Leverage?  [Take a look]:

● 12 million votes.
● Victory in 22 states.
● 45 percent of pledged delegates.
● A history-making small-dollar fundraising campaign that out-raised his well-heeled opponent.

That was all while facing one of the most powerful Democratic clans in history, rejecting big-money donors, and challenging one of the most famous people in the world as a leftist outsider.

bernie 3Leverage? Consider the trend line: Twelve months ago Bernie Sanders was all but unknown nationally. He didn’t fit the typical “politician” profile in age, style, or rhetoric. He was a self-described democratic socialist. And he faced overwhelming obstacles erected by the party machinery at all levels.

bernie 5

This election is not about just the next four years, it’s about our current and future generations.  As I see it, the problems with which our nation and the world have to wrestle, are seemingly insurmountable.  We need new ideas and strategies from our more savvy younger citizens.  The old guard should be retired.  And, at 78, I can say this with some degree of experience.  I admire our young people.  They are vigorous and full of new ideas that are waiting to be put on the table; unlike many of our “tired, old fogeys” who say they represent their constituents, but in reality, represent themselves with their self-interests.

The polls I’ve seen have shown that Bernie had a better chance at defeating Trump than Hillary did.

I look forward to the upcoming Democratic Convention.  It is going to be veerryy interesting, I expect.

I refer you to the following links:

https://ourfuture.org/20160620/bernies-leverage-isnt-going-anywhere-deal-with-it?utm_source=progressive_breakfast&utm_medium=email&utm_campaign=pbreak

bernie 8

https://ourfuture.org/20160619/peoples-summit-attendees-leave-determined-to-keep-the-bern-alive

[Bernie images from bingdotcom]

[ Header image from http://www.freewebheaders.com ]

 

Save

Save

Save

Save

Save

Enough Is Enough

Too much sun is not good.

Pussy Cats 3

We all know that cats sunbathe.  They love to feel the warmth surround and hug them.

There comes a time when even a good thing has to come to an end; when “enough is enough.”

Enough sun I’ve had enough sun.

View original post

Looking Back in Time

Memories…

Pussy Cats 3

As you may remember, Romeo is no longer with us.  I was looking at some past photos and came up with the one below.

It was a rare occurrence when Patches would accept Romeo being so close to her.

Romeo-Patches together Togetherness can be a good thing.

View original post

Beach Time

The sun, sea and sand. What a life!

Pussy Cats 3

Rusty and Patches have never been to the beach.  And never will be.

However, I think, if they use their imagination, they could believe they are there.  Anyway, here are their pretend photos of “At the Beach.”

almost like being at the beach 2 What could be more “beachy” than fish, sun and waves?

almost like being at the beach Patches even has her pretend pink whale to keep her company while she’s “absorbing” some ‘rays.

View original post

Are We Getting Closer To A Myalgic Encephalomyelitis Biomarker?

 

In #MEAction‘s latest announcement, we’ve learned that the National Institute of Allergy and Infection Diseases (NIAID) of NIH recently funded Dr. Derya Unutmaz’s latest grant application.  Dr. Unutmaz is the renowned immunologist at the Jackson Laboratory for Genomic Medicine.

[Dr. Unutmaz’s] research focuses on defining the optimal immune response and what happens during infection and chronic disease.

A few years ago Suzanne D. Vernon, PhD was introduced to Dr. Unutmaz, and knew his research focus was a very good fit for ME/CFS.  Dr. Unutmaz became intrigued with ME and the ongoing research to uncover its mysteries.  He decided to apply to the NIH for funding to expand the numbers of patient samples and types of quantitative analyses on the blood.

The National Institute of Allergy and Infection Diseases (NIAID) of NIH recently funded Dr. Unutmaz’s grant application. He will receive five years of funding – totaling $3,281,515 from the National Institute of Allergy and Infectious Diseases — to find better ways to diagnose and treat ME/CFS. Dr. Lucinda Bateman and Suzanne D. Vernon, PhD are Co-Investigators on this project and the Bateman Horne Center will provide the required blood samples and correlating clinical information for the participating samples.

alien

We need Myalgic Encephalomyelitis information taught in medical schools and information disseminated to all doctors.

For too long, research in ME/CFS has been lean and under-funded for several reasons, including the shortage of accurately diagnosed patients available for research studies. The Bateman Horne Center – a clinic specializing in ME/CFS/FM and with a large number of patients who have been carefully and accurately diagnosed, and continue to be treated effectively – will partner with Dr. Unutmaz so that a Research Ready Army of well qualified patients can participate in this exciting research.

Source:  $3.28 million awarded for ME/cfs biomarker study.

See also:  Bateman Horne Center

[ Header image from http://www.freewebheaders.com ]

[Alien image from bingdotcom]