clifffaith
TUG Member
- Joined
- Feb 24, 2016
- Messages
- 5,763
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- Location
- San Juan Capistrano, CA
- Resorts Owned
- Worldmark
Our previous doctor was part of the Providence system. Blood, urine etc test results would show up after the doctor reviewed them. Since we’ve moved Cliff’s test results from now come from his doctors at UCI through MyChart. Blood test results are near about instantaneous, and since they always draw blood right before his doctor’s appointment we look at the results together with him. I see his quarterly CT results (they are monitoring him to be sure his bladder cancer doesn’t return) about a week after the scans. I always assumed his doctors were seeing those before releasing them, but after seeing an MRI result 24 hours after he had the procedure, it looks like results are being released prior to the doctors reviewing them.
The joke in our home for years has been “how could we ever tell if Cliff has Alzheimer’s, he wanders around in a daze half the time anyway!” He is the quintessential absent minded professor. But over about the last four years, and more significantly in the last year I have seen a lessening of his cognitive skills. He drives with no issue whatsoever, but can’t use his iPhone for anything beyond a phone call no matter how many classes we take here at the Old Folks Home or how many times I show him how to Google something using it. He can play bridge, chess and poker still, but doesn’t know our phone number and comes to me every day (thank God) with various scam emails asking me how to respond to them.
So I think to humor me more than anything else, one of his oncologists said he’d refer us to a neurologist who then sent him for an MRI of his brain. The next day I see the test results (visible to Cliff too, but he doesn’t A) think to look and B) can never get into the system in spite of changing the password DOZENS of times and then not remembering it or writing it down).
Below is what I saw on MyChart which made me think “oh, the doctor doesn’t see this first and hold it so he can intercept bad news and deliver it in person”:
Severe volume loss in the mesial temporal lobes and parietal lobes superimposed on mild generalized volume loss. The findings can be seen in the setting of Alzheimer's dementia.
What the heck? Why would something like this be posted before input from the doctor? I kept this to myself for the next five weeks before his next neurologist appt. In the meantime he went for cognitive testing where he scored 26 on one protocol (or whatever it would be called) where below 26 is cognitively impaired, and 27 on another scale where below 50 is impaired. Yet he scored high on a smell test which apparently he would not have done with Alzheimer’s.
The doctor was noncommittal when we saw him just before Christmas, and never used the word Alzheimer’s, so we don’t really know what is going on. He put Cliff on Aricept (a drug prescribed to Alzheimer’s patients to slow disease progression). Cliff is nauseous (bad) and drowsy (good to sleep if queasy) from the new drug. It didn’t sink in to him that the doctor mentioned side effects, and I haven’t reminded him of this hoping the nausea will lessen as he gets used to the drug. I’m afraid if he realizes the drug is making him queasy he’ll stop taking it. When I first went on statins I had such muscle pain for three days I absolutely would have stopped the drug if I’d made the connection. I figured I had the flu and it was only months later that I read an article that made me realize I’d had temporary side effects.
The joke in our home for years has been “how could we ever tell if Cliff has Alzheimer’s, he wanders around in a daze half the time anyway!” He is the quintessential absent minded professor. But over about the last four years, and more significantly in the last year I have seen a lessening of his cognitive skills. He drives with no issue whatsoever, but can’t use his iPhone for anything beyond a phone call no matter how many classes we take here at the Old Folks Home or how many times I show him how to Google something using it. He can play bridge, chess and poker still, but doesn’t know our phone number and comes to me every day (thank God) with various scam emails asking me how to respond to them.
So I think to humor me more than anything else, one of his oncologists said he’d refer us to a neurologist who then sent him for an MRI of his brain. The next day I see the test results (visible to Cliff too, but he doesn’t A) think to look and B) can never get into the system in spite of changing the password DOZENS of times and then not remembering it or writing it down).
Below is what I saw on MyChart which made me think “oh, the doctor doesn’t see this first and hold it so he can intercept bad news and deliver it in person”:
Severe volume loss in the mesial temporal lobes and parietal lobes superimposed on mild generalized volume loss. The findings can be seen in the setting of Alzheimer's dementia.
What the heck? Why would something like this be posted before input from the doctor? I kept this to myself for the next five weeks before his next neurologist appt. In the meantime he went for cognitive testing where he scored 26 on one protocol (or whatever it would be called) where below 26 is cognitively impaired, and 27 on another scale where below 50 is impaired. Yet he scored high on a smell test which apparently he would not have done with Alzheimer’s.
The doctor was noncommittal when we saw him just before Christmas, and never used the word Alzheimer’s, so we don’t really know what is going on. He put Cliff on Aricept (a drug prescribed to Alzheimer’s patients to slow disease progression). Cliff is nauseous (bad) and drowsy (good to sleep if queasy) from the new drug. It didn’t sink in to him that the doctor mentioned side effects, and I haven’t reminded him of this hoping the nausea will lessen as he gets used to the drug. I’m afraid if he realizes the drug is making him queasy he’ll stop taking it. When I first went on statins I had such muscle pain for three days I absolutely would have stopped the drug if I’d made the connection. I figured I had the flu and it was only months later that I read an article that made me realize I’d had temporary side effects.