All truly great things must eventually come to and end. It is with much sadness that I find that I can no longer be the voice of Command Center.

Like most of you, I work. My current job demands coupled with some family issues has forced me to think about all the hours that I spend online trying to defeat the Democrats

We have come so far from the early days.   We are winning and we will continue to win.  Because we are right and we are Americans. We fight for what we believe in.  It is ingrained in our souls. 

I was always just one small cog in the wheel. Someone will replace me and they will be awesome!

The most important thing is to keep speaking out! Keep educating yourselves.  You no longer need me to do that for you. 

We, as a movement, have come so far we can not let ourselves be taken back to the dark years when we knew what was happening but said nothing.  You have a voice.  You must use it!

I wish you all well and I will be on the boards posting on occasion. But, you will no longer find me in your inbox and I know that some will be happy about that!

Fight on....it is what we do.

Dee

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So sorry to see you go best of luck to you in your future endeavors

Thank you Dee for all you have done. You did a great job. You will be missed.

God Bless you Dee you are an American Patriot.

Shalom

Will miss you Dee.  I pray God will walk with his arm around your shoulder. You have done your duty.  A job well done.

God bless!

Keeper of the Flame...

Sorry to see you go Dee. You have done a fabulous job all these years. You helped a lot of people see the light. Best wishes for you and your family in future.

YOU WILL BE GREATLY MISSED, GOD. BLESS YOU AND GOOD LUCK
Don't you EVER think of yourself as a small cog in the gears! You've been an amazing driving force, and I, for one, am sad, too. But ...life goes on, and your leadership will be missed, but priorities...understandable. God bless, Dee.

You are the best!

DEE: WE SHALL MISS YOU TREMENDOUSLY.  I FORWARDED YOUR POSTINGS TO APPROXIMATELY 50 OTHERS ALL OVER THE WORLD EVERY NIGHT.  I UNDERSTAND YOUR NEED FOR A BREAK.  I HOPE YOU WILL RECONSIDER A COME BACK AT A LATER DATE.  GET SOME WELL EARNED REST.  THANK YOU FOR ALL THAT YOU HAVE DONE.  BILL DAVIS

Try to drop by and post something every now and then....

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ALERT ALERT

SICK: Leprosy On The Rise In Los Angeles 

Ahh, the joys of open borders and Democrat leadership.

California is not just a public toilet but now there is evidence that leprosy is on the rise in Los Angeles County.

Barack Obama changed US law in 2016 and allowed immigrants with blistering STDs and leprosy to migrate to the US.

Medscape reported:

Leprosy, also known as Hansen’s disease, is rarely seen in the United States, but cases continue to emerge in Los Angeles County, a new report says.

“Hansen’s disease still exists, and we need to educate medical students and physicians,” coauthor Dr. Maria Teresa Ochoa from Keck Medical Center of the University of Southern California, Los Angeles, told Reuters Health by email.

Dr. Ochoa and colleagues identified 187 patients with the disease in a review of medical records from their leprosy clinic spanning 1973 to 2018. Most patients were Latino, originating from Mexico, and they experienced a median delay in diagnosis of more than three years, the team reports JAMA Dermatology, online August 7.

Multibacillary leprosy (MB) cases outnumbered paucibacillary leprosy (PB) cases by nearly eight to one (88.6% vs. 11.4%, respectively), and Latino patients were more likely than non-Latino patients to have MB, as were patients from Central or South America (versus other regions).

Most patients (80.7%) received multidrug therapy, and most (92.6%) received antibiotics for more than two years, especially if they had MB.

Only about half of patients (56.7%) had World Health Organization (WHO) grade 0 disability (no signs or symptoms suggestive of leprosy or disability) at the one-year follow-up, whereas 16.0% had grade 1 disability (loss of protective sensation) and 26.2% had grade 2 disability (visible deformity) at the last follow-up.

Among the patients who lost protective sensation, 87.7% (50/57) did not regain it following therapy.

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