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The Long and Winding Road…

~ An Alzheimer's Journey and Beyond

The Long and Winding Road…

Category Archives: Pharma

Let’s not upset the apple cart…

08 Monday Oct 2012

Posted by Ann Napoletan in Blogging, Caregivers.com, Finding a Facility, Long Term Care Insurance, Mom, Pharma, Smiles

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So I returned Friday’s call to the neurologist’s office today. He wanted to bump up her Buspar, and I decided against it. Right now, I see no reason to change anything. Yes, she has had some horrible nights, but since we know there will never be a perfect balance, I have to go with the lesser of two evils. I’d rather a few nights than 24×7. Not taking that risk. We’ll re-evaluate next Monday.

That being said, I got a text from Susie tonight that blew my mind. Mom was on her second plate of meatloaf, potatoes, and carrots. Yes, REAL FOOD. I just told someone today that I doubted she would ever eat “normally” again, and whad’ya know – she proved me wrong! We’ll see if it’s a trend or a fluke, but I am stunned! Who would have ever thought…

The pictures below were texted to me at various times throughout the day. Enjoy!

(And, check out today’s piece on Caregivers – some tips on the dreaded search for long-term care. Major key to success: trust your gut.)

20121008-205800.jpg

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Up, down, and all around.

19 Wednesday Sep 2012

Posted by Ann Napoletan in Heartland, Mom, Pharma

≈ 6 Comments

So, Susie called me this evening with some great news. Mom ate more today than she’s had in the past three weeks combined. Who knew that having 11 grapes, 8 crackers, a piece of toast (minus the crust), a cookie, 2 Ensures, 5 glasses of tea, and an ice cream bar would be worthy of a celebration! May not have hit all food groups, but it’s some solid food, and a LOT of fluids – I’m not complaining.

Trying not to get my hopes up. It was just one day, and she’s still sleeping a lot. Let’s see what tomorrow holds, but I don’t think she’s ready to give up quite yet…

And to think just four days ago, Heartland was on the verge of loading her up with Haldol and turning her into a zombie… 

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A word about patient advocacy…

15 Saturday Sep 2012

Posted by Ann Napoletan in Pharma

≈ 2 Comments

The few times that either of my parents have been in the hospital, it struck me that there were so many people there alone – with no one to advocate for them. Experience quickly taught me just how critical it is to have someone to bridge that gap and to look out for the patient’s best interests, especially in the case of seniors.

Yesterday, I was once again reminded of how important it is to stay on top of things. I got a call from Eason House in the morning stating that the neurologist had faxed orders to dc Mom’s Aricept.

I.was.livid. A week ago, I told the doc that I didn’t want any further med changes without my prior consent. At the time, he had made two rather significant changes, and I wanted to let things alone and allow some time to see how she would do. I have the utmost respect for her neurologist; he’s one of the best in the city as far as ALZ and dementia go, BUT… there have been too many med changes made in succession without a chance to see what is working and what isn’t.

So, a week later, without my consent, he faxes orders to dc the Aricept. WTF?!?

After a call to office, a call to the pharmacy, and a call from the pharmacy to the doc, the orders were cancelled. But what if the folks from Eason House weren’t my second set of eyes and ears? What if they had not let me know what was going on?

I really cannot stress enough how important it is to stay actively involved in long term care. Insert yourself into whatever the situation may be to ensure that you understand (and agree with) the treatment protocol. Science is a wonderful thing, and thank God for medical professionals, but you must not be intimidated by titles. The fact is, sometimes YOU know better than anyone else what is best for your loved one, and there are times when you have to stand your ground, even if it means overruling the experts.

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Marilyn, BA (before Alzheimer's)

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