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mblahnikluver
So I am having a hard time finding a new doctor.
Before I couldn't afford a doctor because I didn't have insurance, now I have it and can't find a doctor that is taking new patients. I have a doctor but I am not happy with her. She isn't listening and all she seems to want to do is write scripts and that is it. She has not discussed any of my test with me. I have to call and beg to talk to her. So I want a new doctor.
I have spent the morning calling doctors only none are accepting new patients and the ones I do find don't take my insurance.
I hate this country...I want out!! It is messed up and nobody cares about your health it's all about friggin money!!!!!!!!
What happened to the doctors that actually wanted to help people? Where did they all go?!
So I have insurance yet i can't even use it. Pissed off.
daryllyn
I feel your pain!
I've been looking for a new Rheumatologist for well over a year. There is only one in my network. All others either aren't taking new patients, or they don't accept my insurance, or they want 400 bucks just for me to walk through the door. Some are even booked a YEAR out. My current one sounds much like yours.. he throws pill after pill at me, doesn't listen, and is very short and cold. Its not fun.
My only advice for you until you can find a new doctor is to make an appointment with your existing doctor and express your concerns to her and see if maybe it makes a difference in the level of care you are receiving. That's what I'm doing at my appointment in December.
amulla8
a chinook helicopter just flew over west ky. over henderson, we arent in thier flight path nor do military ever fly over us,
Yea I had my last doctor order an MRI for my neck and brain. I've had migraines for 5 mths now.
I am having blood work done tomorrow to test for Rheumatoid Arthritis and I dread that result because it does run in my family. I was told I had fybromyalgia but she didn't do anything about it. She wanted to put me on Cymbalta which she said is used to treat Fybromyalgia. I am not a candidate for Cymbalta.
My current doctor has no appts til January which is my next appt with her. I did find a male doctor that can see me at the end of the month. So that is good but I preferred a female. He has a small office which is what i want so that helps. I explained to the nurse my concerns with my current doctor and she said he likes to take time and explain all results which is what I WANT!
butcherguy
reply to post by daryllyn
Have you ever had an eye migraine?
The first time I got one, I went to the doctor. It really freaked me out.
Now when I get one, I think, 'Oh, here is another one of those'. I have never had m any pain associated with one, just disruption of my vision.
I get normal migraines too, but haven't been troubled with them lately.
butcherguy
My toe is hurting today.
I suffer from gout.
But I am not going to my doctor.
He annoys me when I go there.
-Get this blood test.
-Stop smoking.
-Don't eat this and that.
-Limit your intake of alcoholic beverages to this much.
-Go get this prescription and take it forever... sorry about the side effects that are worse than the disease.
butcherguy
My toe is hurting today.
I suffer from gout.
But I am not going to my doctor.
He annoys me when I go there.
-Get this blood test.
-Stop smoking.
-Don't eat this and that.
-Limit your intake of alcoholic beverages to this much.
-Go get this prescription and take it forever... sorry about the side effects that are worse than the disease.
FissionSurplus
Oh, I sympathize with you on this one. Because I have fibromyalgia and rheumatoid arthritis since 1999, I've been through the wringer with doctors, and I have grown to dislike the vast majority of them.
I treat myself with vitamins and herbs, and it has made a world of difference. I went from being basically disabled in constant pain, to virtually pain free. I still have the disease, mind you, but it is well controlled.
Location does have something to do with finding a doctor. However, I had poor luck in larger cities. Same lack of knowledge on my disease, longer waiting time, more money, and the end result was the same. Having moved to a tiny town with a population of about 1500, I found a small rural clinic where the doc will listen to me for 2 hours at a stretch. $45 per visit (I have no insurance).
I used to get bad headaches such as you describe. I used to get put out under general anesthesia, and they shot my neck and the back of my head full of numbing agents. $1000 a pop (I had no insurance then either). Did it work? Not really, just very temporarily. I found that cutting out carbs out of my diet, and supplementing with anti-inflammatory herbs such as Turmeric and Samento, was the real treatment.
Naturally you want to get it imaged to see if there is a problem other than the fibro which is causing your issues, and that is your main frustration now....but if you also clean up your diet of everything that causes inflammation, including veggies in the nightshade family (potatoes, tomatoes, and green peppers...I know, I hated to give those up), you may find your discomfort lessening.
Knowledge is power. The doctors still don't know squat about these autoimmune disorders, you must be your own doctor. Please see: www.abovetopsecret.com...
In the mean time, best of luck on finding one that actually give's a rat's behind about you and your chronic pain.
chiefsmom
My whole family is going through the same thing! It seems that because we didn't need to go to the doctor in two years, we are dropped. I guess he wasn't making enough money off of us.
I cannot believe how hard it is to find a new one. And my son actually found one that was accepting new patients, but you had to wait a month to get in to see them.
I'm afraid it is only going to get worse. Yes, you can have our great new healthcare, that you can't afford, but good luck finding a doctor to see you!
daryllyn
reply to post by mblahnikluver
Yea I had my last doctor order an MRI for my neck and brain. I've had migraines for 5 mths now.
Migraines are the worst thing ever. I've had them ever since I can remember. I have 'waking' migraines; its already in full swing by the time I wake up and I can't take anything for it by that point. Well I could, but it won't stay down, so I don't bother if I wake with one.
In the rare event that I feel it coming, I take tension headache meds (tylenol with caffeine basically) and 800mg of advil. Migraines are literally caused by inflammation around dilated vessels in the brain, so caffeine (vasoconstricts dilated vessels) and advil (NSAID) can help. But my go to is ALWAYS an ice pack on the back of my neck. If you have never tried it, I hope you will give it a shot! Ice and baggies are two things I make sure to never run out of!
As someone with RA, I certainly hope that isn't the case for you. Its rough. Remember that RA cannot be diagnosed through lab work alone. There is a criteria set that takes into account symptoms, signs, and lab results because there is no specific test that 100 percent confirms. For example, some people with RA have negative blood work (for RF factor and Anti-CCP) and they are called seronegative. The Rheumatoid Factor test can mean lots of things and has a low specificity for RA but it DOES have a high correlation, and I imagine that's one you will have ran, probably along with the Anti-CCP, C reactive protein, and SED rate.
I don't agree but I've been diagnosed with Fibro as well and Cymbalta and Lyrica did NOTHING for me but make me feel worse. Maybe some other Fibro people can chime in with what has worked for them.
My current doctor has no appts til January which is my next appt with her. I did find a male doctor that can see me at the end of the month. So that is good but I preferred a female. He has a small office which is what i want so that helps. I explained to the nurse my concerns with my current doctor and she said he likes to take time and explain all results which is what I WANT!
I hope you like him, he might be a great doc! At least if he cares, he can get things approved and fight for you.