Sunrise, through the pines....
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Good Morning All;
Something really F~U~N~K~Y with my computer lately. Running and (reacting) quite choppy. So if I am not "on" you know why.
I apologize for not blogging, having been spending lots of my time doing research on Casey's TP/AIT procedure; and finding people that have gone through this all.
We have not heard back yet; although Casey is to call Dr. Sutherland's office today.
Keep your fingers crossed please.
***Important note to Splat,
Please do not forget to UN~cross those appendages.
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As promised to my restless dogs, and myself,.
we did take that walk back to the woods.
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.....
You do not see Miss Milly because she was on a leash.
Too many hunters around;
(bow, and bunny, and squirrel hunters)
to be taking any chances on her wandering off.
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Notice too, that we came home to disked fields.
(WTH ever happened to plowing a field,- like is suppose to be done)?
At any rate, this proved to be the last walk before the snow came..
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Don't let ANYONE fool you..
These are the only acceptable snowfall amounts.
hehehe
..
......
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I wrote a message for you all.
on the back windshield of the old Buick...
And just to give you a little idea how much "Snow" we got...
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hehehe
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The "Snow" was all gone within an hour or 2..
(Yup. These ARE truly the snowfalls I love)!
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Did I mention my old reliable 1992 Buick Roadmaster?
Stay with me here for a minute...
- Know that I haven't gone for "Chinese" in a while; but if I had, this is the fortune that would have been in my cookie.
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Been fighting the ahem 'urge' to not fly off the toilet and go through the ceiling when I pee. And yes you know me, it's been going on since before we went to Minnesota.
And yes too, I did agree to take the antibiotics for three days.
(Are you proud of me now)?
It is some sulfa (and a HUGE horse) pill. I also take some prescription that turns my pee a very nasty red~orange~rust color. (If I didn't think I was dying before, this surely makes me wonder)?
Back to Monday...
I had that doctor appointment, and afterward had arranged to go pick up my boys.
As I got in the Rendezvous, throwing my winter jacket (and Punk) in the backseat, I turned the key...
...It clicked and the entire panel went black.
NO !! WAIT, dammit, I'm late already...
Not being one to trust that these cars really mean it, I turned the key a few more times. (Just to give it more chances to start).
No go. No way. Just black.
There was also no way that I was forfeiting either the doctor appointment, or the boys. So I did what any other normal (read "desperate") human being would do.
I came back inside, grabbed the keys to the Roadmaster;
(Unlicensed for 3 years, uninsured, & in dire need of shocks).
SO?
So hang on, cuz I gotta "go".
Got Punk in there.
She loves this car, and much prefers the velour seat covers to the leather anyway, (no slippage of dog with braking or cornering).- I turned the key, and it fired right up.
I made the call that I would be late for the Dr., and realized I needed some air in the tires too.
Late. It will have to keep til after.
It did.- And I did not take the boys. Too darned unsafe in that car...
But I did go visit anyway. (Heck I'd gotten to the clinic without being pulled over, what's a few more miles)?
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Master Gabriel!.
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And Baby Sam!
Where on earth did those blue eyes come from?!
And which is the dominant gene, blue or brown?
(9th grade biology escapes me right now).
Hmmm...
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Here's Miss Milly showing a bit of blue...
hehehe
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Casey thought Milly was cold outside.
It was 42° that day, so... NOT.
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Even Mr Sputty shows off a blue~green cast from his eye.
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So he is kinda fat...
Must have been the meeces..
Of which I have seen NONE for the past weeks..
YAY Sputnik!
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Normally, I would tell you what this is all about....
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But THAT'S a whole 'nother blog (tomorrows); and I'd better close for now.
I do promise to try to keep you updated better...
Love to all.
XOXO
Anne
PS
The BLUE in today's counter (below) is as close to real on Baby Sam's eyes as I could find...
Anna~Anna
"Flintville Annie"
© 2006-2015
Eyeballs. Animals. Cars. Weather...
RECALL- Aluminum Fragments in NESTLE Strawberry QUIK
http://www.fda.gov/oc/po/firmrecalls/nestle11_08.html
Nestlé USA is voluntarily recalling two (2) production codes of Nestlé Nesquik Strawberry Powder 21.8 ounce that may contain small fragments of aluminum.
The recall only includes two (2) production codes of 21.8-ounce containers of Nestlé Nesquik Strawberry Powder. Printed on the bottom of each plastic container is a production code of "82255880" or "82265880" with a best by date of "August 2010."
No other Nestlé Nesquik products or production codes of Nestlé Nesquik Strawberry Powder are affected by this recall.
The products were produced on August 12 and 13 and were distributed in the U.S. and in Puerto Rico.
Consumers who have this product at home can return it to the store where it was purchased for a refund.
Consumers with questions about the recall should call Nestlé Consumer Services Center at 888-637-4345.
Nestlé apologizes for any inconvenience experienced by our valued consumers and retail customers.
Contact (Media):
Pam Krebs
Nestlé USA
818-551-3362
Nestlé USA is voluntarily recalling two (2) production codes of Nestlé Nesquik Strawberry Powder 21.8 ounce that may contain small fragments of aluminum.
The recall only includes two (2) production codes of 21.8-ounce containers of Nestlé Nesquik Strawberry Powder. Printed on the bottom of each plastic container is a production code of "82255880" or "82265880" with a best by date of "August 2010."
No other Nestlé Nesquik products or production codes of Nestlé Nesquik Strawberry Powder are affected by this recall.
The products were produced on August 12 and 13 and were distributed in the U.S. and in Puerto Rico.
Consumers who have this product at home can return it to the store where it was purchased for a refund.
Consumers with questions about the recall should call Nestlé Consumer Services Center at 888-637-4345.
Nestlé apologizes for any inconvenience experienced by our valued consumers and retail customers.
Contact (Media):
Pam Krebs
Nestlé USA
818-551-3362
RECALLED- Nestle, PESTICIDE IN CEREAL.
http://www.fda.gov/oc/po/firmrecalls/nestle211_08.html
Nestlé Withdraws Nestlé Farinha Lactea Cereal in the United States
Contact:
Nestlé USA Corporate
(818) 551-3284
FOR IMMEDIATE RELEASE -- November 3, 2008 -- Nestlé is withdrawing Nestlé Farinha Lactea cereal in the United States. Nestlé is taking this action as we have learned that the product may contain residual traces of a pesticide not currently approved for use on wheat in the U.S. While the pesticide is approved for use in Brazil and the noted levels are well below Brazilian standards, it is not used on wheat products in the United States and therefore there is no set standard for its presence in cereal. The pesticide is permitted in the United States on grain crops other than wheat.
Nestlé Farinha Lactea cereal is manufactured in Brazil by Nestlé Brazil and sold primarily in Portuguese language communities in the United States. The withdrawal applies to all sizes, varieties and production codes of the product. No other Nestlé products are affected.
Nestlé USA is assisting with the withdrawal of this product from the U.S. market to ensure the continued quality and safety of Nestlé products. Nestlé has not received any illness reports or consumer complaints.
Consumers who have purchased Nestlé Farinha Lactea cereal should not consume the product, and should return it to the store where they purchased it for a full refund.
We encourage consumers with questions about the withdrawal to contact Nestlé Consumer Services at (800) 628-7679. Media should contact Edie Burge at Nestlé USA Corporate & Brand Affairs at (818) 551-3284.
Nestlé Withdraws Nestlé Farinha Lactea Cereal in the United States
Contact:
Nestlé USA Corporate
(818) 551-3284
FOR IMMEDIATE RELEASE -- November 3, 2008 -- Nestlé is withdrawing Nestlé Farinha Lactea cereal in the United States. Nestlé is taking this action as we have learned that the product may contain residual traces of a pesticide not currently approved for use on wheat in the U.S. While the pesticide is approved for use in Brazil and the noted levels are well below Brazilian standards, it is not used on wheat products in the United States and therefore there is no set standard for its presence in cereal. The pesticide is permitted in the United States on grain crops other than wheat.
Nestlé Farinha Lactea cereal is manufactured in Brazil by Nestlé Brazil and sold primarily in Portuguese language communities in the United States. The withdrawal applies to all sizes, varieties and production codes of the product. No other Nestlé products are affected.
Nestlé USA is assisting with the withdrawal of this product from the U.S. market to ensure the continued quality and safety of Nestlé products. Nestlé has not received any illness reports or consumer complaints.
Consumers who have purchased Nestlé Farinha Lactea cereal should not consume the product, and should return it to the store where they purchased it for a full refund.
We encourage consumers with questions about the withdrawal to contact Nestlé Consumer Services at (800) 628-7679. Media should contact Edie Burge at Nestlé USA Corporate & Brand Affairs at (818) 551-3284.
RECALLED- BABY Gas Relief Drops
http://www.fda.gov/oc/po/firmrecalls/johnsonjohnson11_08.html
Johnson and Johnson--Merck Consumer Pharmaceuticals Company Announces Urgent Voluntary Nationwide Recall Of Infants' Mylicon Gas Relief Dye Free Drops (Simethicone-Antigas) Non-Staining Due To Possible Metal Fragments
www.mylicon.com
Johnson and Johnson--Merck Consumer Pharmaceuticals Company Announces Urgent Voluntary Nationwide Recall Of Infants' Mylicon Gas Relief Dye Free Drops (Simethicone-Antigas) Non-Staining Due To Possible Metal Fragments
Media Contact:
Marc Boston
215-273-7649 (office)
215-429-7034 (mobile)
Bonnie Jacobs
215-273-8994 (office)
856-912-9965 (mobile)
FOR IMMEDIATE RELEASE -- Fort Washington, PA (November 7, 2008) – Johnson & Johnson • Merck Consumer Pharmaceuticals Company (JJMCP) is voluntarily recalling approximately 12,000 units of Infants' MYLICON® GAS RELIEF DYE FREE drops (simethicone-antigas) non-staining sold in 1 oz. plastic bottles that were distributed after October 5, 2008 nationwide. The company is taking this action in consultation with the U.S. Food and Drug Administration (FDA). Although the potential for serious medical events is low, the company is implementing this recall to the consumer level as a precaution after determining that some bottles could include metal fragments that were generated during the manufacturing process. If any medical events were to occur, most are expected to be temporary and resolve without medical treatment. Parents who have given the product to their infant and are concerned should contact their health care provider immediately.
The two lots of Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining 1 oz. bottles included in the recall are:
Product
Code #
Lot #
Exp
Product
71683791111-1
SMF007
09/10
Infants' Mylicon® Gas Relief Dye Free Non-Staining Drops 1 oz.
71683791111-1
SMF008
09/10
Infants' Mylicon® Gas Relief Dye Free Non-Staining Drops 1 oz.
Consumers can find the lot numbers on the bottom of the box containing the product and also on the lower left side of the sticker on the product bottle.
Consumers who purchased Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining included in this recall should immediately stop using the product and contact the company at 1-800-222-9435 (Monday – Friday, 8:00 a.m. – 8:00 p.m. EST) or via the internet at www.mylicon.com for instructions regarding how to dispose of the product and request a replacement or refund.
Infants' MYLICON® drops are sold over-the counter, in retail stores and pharmacies, as an anti-gas medicine to relieve the discomfort of infant gas frequently caused by air swallowing or by certain formulas or foods.
The recall does not affect any Original Infants' MYLICON® GAS RELIEF products (1/2 oz. or 1 oz. size) or Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining (1/2 oz. size).
The manufacturer has instructed retailers and wholesalers to return their inventories.
Johnson and Johnson--Merck Consumer Pharmaceuticals Company Announces Urgent Voluntary Nationwide Recall Of Infants' Mylicon Gas Relief Dye Free Drops (Simethicone-Antigas) Non-Staining Due To Possible Metal Fragments
www.mylicon.com
Johnson and Johnson--Merck Consumer Pharmaceuticals Company Announces Urgent Voluntary Nationwide Recall Of Infants' Mylicon Gas Relief Dye Free Drops (Simethicone-Antigas) Non-Staining Due To Possible Metal Fragments
Media Contact:
Marc Boston
215-273-7649 (office)
215-429-7034 (mobile)
Bonnie Jacobs
215-273-8994 (office)
856-912-9965 (mobile)
FOR IMMEDIATE RELEASE -- Fort Washington, PA (November 7, 2008) – Johnson & Johnson • Merck Consumer Pharmaceuticals Company (JJMCP) is voluntarily recalling approximately 12,000 units of Infants' MYLICON® GAS RELIEF DYE FREE drops (simethicone-antigas) non-staining sold in 1 oz. plastic bottles that were distributed after October 5, 2008 nationwide. The company is taking this action in consultation with the U.S. Food and Drug Administration (FDA). Although the potential for serious medical events is low, the company is implementing this recall to the consumer level as a precaution after determining that some bottles could include metal fragments that were generated during the manufacturing process. If any medical events were to occur, most are expected to be temporary and resolve without medical treatment. Parents who have given the product to their infant and are concerned should contact their health care provider immediately.
The two lots of Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining 1 oz. bottles included in the recall are:
Product
Code #
Lot #
Exp
Product
71683791111-1
SMF007
09/10
Infants' Mylicon® Gas Relief Dye Free Non-Staining Drops 1 oz.
71683791111-1
SMF008
09/10
Infants' Mylicon® Gas Relief Dye Free Non-Staining Drops 1 oz.
Consumers can find the lot numbers on the bottom of the box containing the product and also on the lower left side of the sticker on the product bottle.
Consumers who purchased Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining included in this recall should immediately stop using the product and contact the company at 1-800-222-9435 (Monday – Friday, 8:00 a.m. – 8:00 p.m. EST) or via the internet at www.mylicon.com for instructions regarding how to dispose of the product and request a replacement or refund.
Infants' MYLICON® drops are sold over-the counter, in retail stores and pharmacies, as an anti-gas medicine to relieve the discomfort of infant gas frequently caused by air swallowing or by certain formulas or foods.
The recall does not affect any Original Infants' MYLICON® GAS RELIEF products (1/2 oz. or 1 oz. size) or Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining (1/2 oz. size).
The manufacturer has instructed retailers and wholesalers to return their inventories.
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