Clinic Visit
Today Dennis and I had an appointment at the local health clinic. It would be the first time that we would meet our new primary health provider.
Dennis does see the VA health providers at the VA clinic here in town on a yearly basis but it feels good to have a local clinic connection as well. All of Dennis’ meds were gone over as well as having them renewed for a year. Two of his daily meds are gotten from the VA pharmacy in Minneapolis. The cost of those meds are $15.00 per month, which is much less than our Lewis Drug prices would be. We found out this morning, that our primary could also work with the VA for the yearly renewal. Sweet.
When Dennis’ official appointment was completed, he went out to the car for a wait.
It was my turn. Three months ago I did have a med added as my blood pressure read high . . . three times it was taken and always read high. I have been on the additional med for the three months and I have cut back significantly on my caffeine intake. The blood pressure reading was 118/70. Everyone was happy . . . most of all me. My heart does not need any more pressure put upon it than necessary. My lungs and heart were listened to and all was well, along-side of a look in the ears, eyes, nose and throat. I do have to return next Monday for a pee test as I am on an opioid. The opioid is for the discomfort . . . strike that . . . for the pain of the arthritis in my back, hips, feet and hands. The dose is a 50 mg tablet three times a day. No . . . there in no way I can remain active to offset the pain all the time. I know when enough is enough. I do not seek any other remedy for the arthritis. There is always a mention of some possible surgery to take out or deaden nerves in the effective areas. I say no, what may remain could be worse, meaning less mobility or use than what I have now. I want my life, my days to be as mobile as possible. For that, I will take my catheter and pee in a cup.
Even now, since the stroke in 2021, my left side experiences jolts as if the nerves are trying to engage into normal movement. My brain works overtime. If this happens, it is at night after supper when I am less active. My left side will literally jump at bit. When I experience restless leg syndrome, it is always on the left side. I have a prescription for gabapentin for just such events. I don’t take the 800 mg every late day. I gauge each day on its own. Yesterday, when my day didn’t start until 10:30, I had just given in and taken the extra rest. With meds, if the system relies on them too much, they may no longer be effective and then what? A stronger dose? Not for me for now.
Well . . . no secrets in the days of life of this Grammie. I feel very fortunate each and every day.
Meeting the new primary and all my cards laid out for review, I feel very comfortable with her. Dennis agreed.
With that I will take my leave. ♥