Both of my parents have tested positive, Shreveport, LA, USA

4 years ago

Both of my parents have tested positive, Shreveport, LA, USA

Shreveport, Louisiana, United States

Both of my parents have tested positive for COVID-19 and my mom is on a ventilator. My head has been hurting for five days.
They don’t wanna test me bc I don’t have any symptoms. Honestly I haven’t even been eating like i use to.? I AM NOT OKAY

#coronaviruscovid19 #coronaviruscovid19deniedtesting #shreveport #louisiana #us

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I was staying at a shelter in Lockport Cares and there was a Christian pastor at the shelter. Guess again. I dialed an ubulanxe to go to the hospital because my teeth were bleeding.and I was coughing up blood. The woman told me I should not stay … See More
at Lockport Cares because I called an ambulance to go to the hospital.

I assume Lockport cares is possibly food poisoning people. Lockport cares gives you bag lunches , breakfast and dinner.

For 2 nights there is always corn or brownies during Bible study at 8pm at night.

I'm not allowed back because I claaid they were food poisoning people
I told the police when I dialed the ambulance.

My blood sugar was low and I was coughing up blood and my teeth were bleeding.

Warning. Lockport Cares does food poisoning


Also there is a hazard for COVID 19. The manager allows COVID 19 positive to stay there without mandatory mask
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Lockport cares should be shut down for biohazard. Covid positive wear no masks. A mask is not required for covid positive people.

Warning.  | Symptoms: Cough
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Detect, Inc. is voluntarily recalling specific lots of the Detect Covid-19 Test™, their molecular, over-the-counter test used to identify SARS-CoV-2 (the virus that causes Covid-19) in self-collected nasal swabs. The recall affects a total of 11,102 tests shipped to customers from July 26th, 2022 through August 26th, … See More
2022. The test was granted Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) on October 28, 2021. To date, Detect has not received any reports of false negative results related to the affected lots and is issuing this recall out of an abundance of caution.

There is an increased chance that the tests from the lot numbers listed below may give false negative results. Detect has conducted a thorough investigation to identify this issue and has made the decision to conduct a voluntary recall for these lots. The reliability of positive test results is not affected.

Below is a list of the affected lots. The lot number can be found on the side of each test box along with the Use By date.
Lot Number: HB264, Use By Date: 1/1/2023, Number of Tests Shipped: 7,382
Lot Number: HY263, Use By Date: 1/1/2023, Number of Tests Shipped: 1,800
Lot Number: HY264, Use By Date: 1/1/2023, Number of Tests Shipped: 1,920

There is an increased chance that the tests from the lot numbers listed below may give false negative results. Detect has conducted a thorough investigation to identify this issue and has made the decision to conduct a voluntary recall for these lots. To date, Detect has not received any reports of false negative results related to the affected lots and is issuing this recall out of an abundance of caution. The reliability of positive test results is not affected.

Detect is notifying all customers and distributors affected by the recall. Anyone in possession of any unused tests from the affected lots should dispose of the tests. The outer packaging is recyclable while all the test components can be discarded as regular trash. Detect Hubs are not affected by the recall and do not need to be discarded.

Test users who attempt to use recalled tests will be notified in the Detect App™ that the test has been recalled and may not be used.

Detect, Inc. will issue a refund* for the affected tests (as verified by Detect) upon customers’ acknowledgement of receipt of the recall-related communication and confirmation that any affected tests in possession have been disposed of.

Company name: Detect, Inc.
Brand name: Detect
Product recalled: Over the counter Covid-19 Test
Reason of the recall: There is an increased chance that the tests from the lot numbers listed below may give false negative results
FDA Recall date: December 12, 2022

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-three-detect-covid-19-test-lots
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According to Southwestern Electric Power Power outages affected about 13,106 customers in several counties in their Louisiana service area on Tuesday morning Apr 9. The most affected areas are Caddo Parish, DeSoto Parish, and Bossier Parish. The cause of the outage is related to the severe weather … See More
in the area. Crews are working to restore power to the customers affected.

Outage link: df2ov8zclcsoo.cloudfront.net/external/default.html?address=DeSoto+COUNTY+LA&showCountyLayer=true
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According to the Southwestern Electric Power outage map, power outages affected customers in Shreveport on Wednesday morning, Mar 20. The first outage is near Midway Avenue affecting 381 customers. The estimated time for restoration is 1:30 p.m. CT. The second outage is affecting 542 customers near Springlake, … See More
University Terrace. The estimated time for restoration is 1:00 p.m. CT. Crews are working to restore power to the area.

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Power outages are being reported across the ArkLaTex in the wake of storms that pushed through the region late Thursday 14th and early Friday 15th. At 9 a.m., more than 3,000 SWEPCO customers were reporting outages. The most affected area is Shreveport in Caddo Parish with 1,779 … See More
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Recent Interesting Reports

In direct response to the Nurse Assist, LLC voluntary product recall initiated on November 6, 2023, for saline and sterile water medical products, Medline Industries, LP initiated a nationwide recall on November 15, 2023, for its Medline and Centurion branded convenience kits containing Nurse Assist 0.9% Sodium … See More
Chloride Irrigation USP and Sterile Water for Irrigation USP. The Nurse Assist recall was issued due to the potential for a lack of sterility, which could result in non-sterile products. Medline Industries, LP has received one adverse event associated with product manufactured by Nurse Assist.

Water-based medical products that are non-sterile and potentially contaminated could cause serious or life-threatening infections, including bloodstream, urinary tract, open wound/soft tissue, and respiratory infections. Patients who are elderly, critically ill, have weak immune systems (including newborn infants, pregnant women, and cancer patients), or have chronic diseases are particularly at risk of infection. However, other patients could also develop infections after exposure to contaminated water-based medical products.

The recall affects Medline and Centurion convenience kits that may be used at home by patients, caregivers, and home health providers, as well as convenience kits that may be used in medical settings for surgery or other medical procedures. Recalled kits include, but are not limited to, wound care kits, tracheostomy kits and catheter kits. A detailed list of recalled Medline and Centurion convenience kits, as well as an example of product labeling, can be found in the link below.

Consumers who have recalled product should stop using the product and contact Medline immediately.

Medline Industries, LP notified its direct distributors and consumers of the Nurse Assist recall by First Class Mail and email on 11/16/23, upon receipt of initial recall notification from Nurse Assist. Customers who received the recalled product were given instructions to quarantine all affected products immediately and provide Medline with a response regarding the affected quantity on hand. Upon confirmation of the affected quantity, Medline provided customers with over-labels to place on the affected inventory, with instructions for staff to remove the affected component before using the kit. The recall notification also instructed distributors and those who resold or transferred affected product to another company or individuals to notify their customers of this recall notification.

In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: Medline Industries, LP
Brand name: Medline and Centurion
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The Public Health Agency of Canada (PHAC) is investigating a Salmonella outbreak linked to snakes and feeder rodents across eight provinces. The outbreak has resulted in 70 confirmed cases of illness, 10 individuals have been hospitalized, and one fatality reported. The provinces affected include British Columbia (3), … See More
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Many of the individuals who fell ill reported direct or indirect contact with snakes and feeder rodents before their illnesses occurred. Some did not handle the animals themselves but lived in the same house where they were kept. A single common supplier of snakes or feeder rodents has not been identified, indicating that Salmonella bacteria can be found in many species of animals, including snakes and feeder rodents.

The outbreak, which spans from British Columbia to Newfoundland and Labrador, has been ongoing since February 2022. The infected individuals range in age from 0 to 96, with 19% of the cases involving children 5 years or younger.

The issue was first identified due to an increase in reports of Salmonella illnesses across Canada. Through the use of whole genome sequencing, it was determined that some illnesses dating back to 2022 were caused by the same outbreak strain as the illnesses that occurred in 2023 and 2024. The investigation is ongoing, and recent illnesses continue to be reported to PHAC.

You can get sick with Salmonella by touching reptiles and rodents, their food, and their environments and then touching your face, eyes, or mouth without washing your hands. To prevent further spread of the disease, individuals are advised to practice good hand hygiene and frequent handwashing after contact with snakes, feeder rodents, and their environments.

In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Source: www.canada.ca/en/public-health/services/public-health-notices/2023/outbreak-salmonella-infections-linked-snakes-rodents.html
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Heather's Motty, 2207 Summit Avenue, Union City, NJ, USA

1 week ago reported by user-gftfm286

I have received 2 different packages from Heather's Motty which I did NOT order. I will admit that I had looked at the product but because of my resent weight loss I wasn't sure of the size I should get so I never actually order this product, … See More
however have received 2 separate orders. What can I do to return and receive my money back?
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I received a package from Heather's Motty from Heathers Motty 2207 Summit Avenue, Union City, NJ. The return address is associated with YUANHENG AAA, LLC which appears to be a Hong Kong based trading and fulfilment company. The company also has an affiliate in Flushing, NY I … See More
have ordered products from China based companies, but not recently, and did not order these items.
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user-wjtnd218

How do I return something .

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