Good morning, everyone.
Though I would post an update on my medical situation, since so many of you were so kind to respond to my thread. I sincerely thank you. Particular thanks to those who suggested that they had had good results when being seen by a Nurse Practitioner. I would not have consented to be seen by an NP without your good thoughts.
Update:
Had tried to schedule an appointment online this past Monday morning with my doctor, the only appointment I could get was nearly six weeks out. So phoned the office, seeking an appointment, and was told that my doctor would be in the office on Thursday, and would I like to see him then. I happily said "yes", was told that someone would phone me back with an appointment time later that day (again, this was Monday).
I waited all day Monday, and all day Tuesday, for a call-back that never came. Wednesday morning I telephoned to find out what time my appointment was scheduled for the following day (Thursday). After a lot of hemming and hawing (and about ten minutes "on hold") the scheduler came back on the phone and said that in order to get me in on Thursday, would mean that my doctor would be double-booked, so my appointment had been declined by my doctor (!). I was then asked if I would like to see an NP instead, and agreed to see the NP - which I never would have done without reading your positive experiences about your own visits with an NP.
The appointment with the NP was very positive. She really did ask me a lot of questions, spent a considerable amount of time with me (especially since I insisted that I
did not want to take any drugs for this pain, that my main interest at the moment was just trying to find out the
cause of this pain) and we talked a bit about my options and possible reasons for my symptoms. Since I had never had this done before (she asked if I had or had not) a blood test was run to see if I had any kind of auto-immune disease (such as arthritis or Lupus, both of which could cause the joint pain I have been having).
She also said that if I am negative for this, I might just need to face the fact that my discomfort is due to the aging process. I laughed, and agreed this might be the case - but, again, I spent a week in Yellowstone last May, where I walked for many pain-free miles. Just now I have joint pain just walking across the room. So I do have my doubts. Could, of course, still be age-related, but since this pain has come on, and slowly worsened,
only since my Yellowstone trip (where I was attacked by clouds of mosquitoes while hitching up my trailer), I do have my doubts. I doubt that age-related joint pain could have come on relatively suddenly.
I just pulled up the test results online, and the test for auto-immune disease was totally negative. A very good thing, really. The results didn't even show a number, it was just totally negative. A relief there, for sure.
But it doesn't go anywhere to find out why I am having pain. At the time of my cellulitis last summer (I also had a respiratory infection along with, and at the same time, as the cellulitis), as I said before I was extremely ill and debilitated for about four weeks, six weeks before I began to again feel like myself. I was on heavy-duty doses of two different antibiotics during this time, neither seemed to have much effect the course of my infection.
Near the end of the six weeks, I was finally able to get in to see my regular doctor, and his thought was that my infection (both cellulitis and respiratory) were virus, since the antibiotics seemed to have little effect. We discussed the fact that there are many different pathogens that exist in mosquitoes in the Rocky Mountains (where Yellowstone is located), he didn't really know which of these to test for, and (in any case) it was more than likely that the virus had now cleared from my system, so any test would likely prove negative.
Still waiting for the test result for Lyme disease. I was not tested for West Nile Virus (or for any other virus) at the end of my cellulitis infection when I was finally able to see my own doctor due to the time delay. When I first became ill, when I explained that I thought my cellulitis was the result of a mosquito bite that I received in Yellowstone, all they heard was "mosquito bite". No one heard the "Yellowstone" part. Mosquitoes are a big problem in my area as well.
I even had one call screener, when I first became ill, tell me (sounding incredulous): "You want to come in to be seen only because you have a
mosquito bite?!?"
So there you have it. At least for now, I am not ready to accept that I am having pain on walking is solely age-related. I did some searching online, and joint pain does not appear to be one of the lingering effects of West Nile Virus. Something called Chikungunya virus does attack the joints. I will need to research where it occurs in the U.S. - although it is rare here, it has appeared in some places. It is a virus spread by mosquitoes. If anyone has had it, or has heard about it, please let me know.
I guess it is up to me to find out what is going on with me. Which is, of course, always the bottom line in such things.
BirdbyBird wrote:I don't have the circumstances of limited medical options. I have used a Nurse Practitioner for the past 8 years maybe. After my MD left the practice to join a boutique practice which was much better for her family life.
. . . A week later I turn up calling with the Bells Palsey issue. Again after talking to their nurse in reception they got me in.
. . . I am thinking that your idea to move can't come quick enough, except that you are having difficulty moving.
Thank you, Tina, for your thoughts. Very helpful to read that you had a good experience with an NP. Thought I would mention that in researching my own problems, that Bell's Palsy came up as a possible side effect of Lyme Disease. As for moving - I still want to move, but can't at the moment face the thought of moving until I can resolve the pain issue. I can barely do usual housework. Packing for a move pretty much out of the question.
BarbaraRose wrote:Lymes disease can be very serious if not treated right away. I have a friend who died from it because he was misdiagnosed until it was too late.
Thanks for your comment, Barbie. Scary thought. Keeps me motivated to keep doing my research on this.
JudyJB wrote: Are you being a "good" and polite patient? Maybe you should not be. Have you told them that you are having more and more pain and difficulty walking? Tell them you think you might have
Thanks, Judy. Yes, I am generally a "good" and "polite" patient. When I have tried to be otherwise, tried to be forceful and more of a self-advocate, it has seemed to just make getting an appointment to be made more difficult. It has seemed that they listen to me less, not more.
monik7 wrote:Regarding Kaiser: I realize it’s not close to you, but at least you could most likely get an appointment. Kaiser Senior Advantage would become your Medicare supplement, but I think you’d have to make the change from your current supplement soon as there are only a few days left in the open enrollment period. Could you try it for a year?
Sandi
Thanks, Sandi. After reading your post, I did try to find out if I could switch to Kaiser. My zip code is not listed in the areas covered by Kaiser, thus I am not eligible to be covered by Kaiser (
careful - this link will not open in my browser, it just automatically downloads the .pdf to my computer):
https://medicare.kaiserpermanente.org/medicare/pdfs/2019/ca_ncal_SB_PBP1351.pdfAcadianmom wrote: The walk-in clinics are just about useless unless you have a cold or want a flu shot. Martha
Thanks, Martha. I agree 100%
havingfunnow wrote: . . . All of which leads me to believe you'd be better off with a different doctor from a different system!
Thanks, Louise. A different system is, unfortunately, out of the question. Sutter North basically has a lock on medical care in my area. My recent experience with the NP was a good one, though, so perhaps I will stick with her. Certainly easier to get an appointment than with my regular doctor.
Redetotry wrote:So sorry you are having these problems with doctors Anne. It is the same here, hard to get an appointment and if you press, they just say go to Urgent Care. The Urgent Care is only staffed by PA"s. . . .I can barely understand my primary physician and she has been in this country at least 30 years.
. . . I think most doctors tend to over medicate because they are paid by the pharmaceutical companies to prescribe certain drugs. You can go online and find out how much your doctor receives each year from big Pharm.
Thanks for your comments. I agree with what you say here, including the difficulty understanding some care providers. As for being referred to Urgent Care - this just brings me back to the feeling of age-discrimination. Plus, Urgent Care can charge insurers at a higher rate, because your problem is "urgent"
![Rolling Eyes :roll:](./images/smilies/icon_rolleyes.gif)
and not just a "regularly scheduled" appointment. $$$
Just thought I would mention that I also have (as many of you do) AARP United Healthcare as my Medicare Supplement. I have had them about two years now, and have been very happy with them. All of my bills not paid by Medicare have been paid by United Healthcare, no questions asked.
Thanks again to all who have responded to this thread, apologies to you if I may have missed replying to you directly. All of your comments are valuable to me, so thank you very much.
Best wishes,
Anne