I never new that serving my country, could be such a disgrace.
Here in Minnesota im a 4th class citizen i hove no rights under state law .. i need an attorney but i dont have the money for it . I can represent my self in court but im not in titled to an attorney state or VA no help anywhere . Im glad i agave up my freedoms for a socialist state so i can become lesser that shit.
Thank you minnesota , thank you for letting me know were my place is

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Pretty much where all of us are, Andrew.  We are still the unrespected "deplorables, rascists, homophobes" and there is no one yet in the media who gets that we are being ignored, trampled on, taken for granted, plundered, and we have lost our safe spaces, all while unelected heads of illegal government agencies dream up more ways to plunder and control us through regulation strangulation. We have turned into a "Mother May I" permission state.

No one cares except us, and TRUMP! and his Cabinet.

If their crap keeps up, something is going to have to happen. And if it does, we need to band together under the Constitution and fight like hell to bring back common knowledge of it and of our Christian heritage, otherwise known as our birthright.

No one is helping me either, in my difficulties....except my Lord and Savior, Jesus Christ,

Thank God.




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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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