So far, I have lost 6kgs (13lbs 4oz) in 6 weeks. My appetite, which has never been all that great, has reduced a bit, but I am still pretty much staying with the same things I have been doing. Dr told me not to change what I have been doing, because I have been doing everything right.
So far, I have lost 6kgs (13lbs 4oz) in 6 weeks. My appetite, which has never been all that great, has reduced a bit, but I am still pretty much staying with the same things I have been doing. Dr told me not to change what I have been doing, because I have been doing everything right.
Dr N looked at my M.R.I. and said that at the very least, I should have gotten a kneecap replacement. The excuse Dr R gave me, lose some weight, is really a brush off. HE'S worried about a bad outcome. Dr R completely disregarded the fact that I had an above average, excellent outcome with my right knee replacement, and shunted me off to a pain doctor. Why? because he thought I would fuck up his surgical record of successes.
So, their remedies are to pile more drugs on me, or tell me I'm not exercising enough. I have sweat and chafe rashes in place I won't mention because of exercising.
Dr N said from my records, I'm doing all the right things to shed weight healthily, and something else needs to be done. Instead of plying me with more pain killers, we could start with directly injected into the joint medications. Either platelets or SynVisc.
Wish me luck.
Saw Dr L today
Apr. 8th, 2021 05:40 pmI'd felt last time that D L had a chip on his should regarding my husband calling and nagging him to push my appointment up. And that it was reflected in how talked at me, instead of to me. All fixed.
He says that concerning my knee problem, I have 'realistic expectations'. I'm not looking for my knee to magically feel all better. What I want is the pain level of 5 to 7 on a daily basis to lurk around three. I'm functional at that pain level. And I need a good night's sleep. Dr L has given me a prescription that I am to have filled one month after taking 60mgs of Duloxetine a day, a low dose of something (forgot the name) to take around 7pm, in hopes it makes sleeping easier.
Also told me no need to split the Dulox 30mg caps to one in the morning and one at night, but to take the full 60 in the morning.
I told Dr L I was beginning to feel like a pharmaceutical experiment. He said basically, that's true. We are trying to find the right combination to get the nerve pain under control
Tick tock tick tock tick tock
Mar. 15th, 2021 06:12 pmI've had three different doctors, specialist, etc etc, look at my knee and I will sum up their findings:
My knee is borked enough to make my life rather miserable, keeping me mostly housebound, or on just short trips, with a healthy dose of neuropathy, but not bad enough to have remedial surgery/measure.
I'm trying to stay upbeat, but I'm tired. Tired of plastering a smile on my face, putting up cheery conversation, when all I really want to do is put my head under a pillow and cry.
I am on medications galore, and one of them makes me queasy, dizzy, dry mouthed, and drowsy. Two others make me drowsy, another will give me horrible acid reflux unless enough 'with food' is eaten. And two of them give me another problem, but I'm going to give that description a miss.
I've been told that the symptoms from the first one I described 'should' go away after a few weeks. Anyone else ever want to ask the doctors "Define 'a few weeks', please."?
I will muddle through, leg propped on foot stool, Loki snugged up next to me, and hope for the best.
It takes a specialist
Nov. 13th, 2019 03:11 pmFor 19 years I have been asking 4 different GPs to please get my records from Dr R, an endocrinologist in Florida regarding my hypothyroidism, and how it was being successfully treated in the U.S. 4 different GPs, and all I got was hemming and hawing, and my weight going up and up and up, no matter what I did.
I kept food diary for a month.
It wasn't believed.
I wore a pedometer for a month. 30k steps per day on average. But still, I could get no where with my GPs to prescribe me the medication that Dr R did, or even contact Dr R for my records (I had signed a release form, so that couldn't have been the problem)
Today, after a consult with my osteo surgeon, Mr S., regarding bariatric surgery. I told him that I had been under the knife for the past 4 years in one way or another. I want a gap year. There is also the fact that I have FND, and surgery could start triggering it again. Also, I have a history of anorexia. Turning me into an instant anorexic by get gastric sleeving done isn't a great idea.
So, I told him about Dr R, the endocrinologist in Florida. I told Mr S the above history with my GPs, and he said again, this just won't do! I get to fast, and get a Thyroid function test, not just testing to see if I have the Thyroxine in me. Will also get a BGL test, too. Once those results are in, I will be FINALLY seeing an endocrinologist!
Halli-fucking-luiah!
Had a good conversation with my GP today
Apr. 9th, 2019 04:37 pmDiscussed the Lorazepam. I told him I was taking half of what he proscribed. I had tried with the two tabs, three times a day, but I was just too wonked out. I told him I discovered that a sharp, loud, sudden sound would start to trigger a seizure. Even watching a car accident on TV would make my leg and arm start twitching. Discovering one seizure trigger is a good thing.
Got my flu shot, and my arm is already sore, but it was something I expected. Ordered vaccination for shingles, which is currently in my fridge, as I have to wait a few weeks between vaccinations.
Oh, yes, forgot, told him about doing 30 minutes a day on my stationary bike, and how it makes the tendons in my leg feel very stiff and sore. He suggested I get an elliptical trainer. It will be discussed with Wing, and I will try one out first. If my leg can't handle the elliptical treadmill/trainer, I can still keep using the stationary bike.
New day, new medication regime
Mar. 13th, 2019 11:02 amI've been off the Ativan, an on half doses of Lorazepam for a while, mostly because I would forget to take it. I was told it would take a few days for the Lyrica to work. Joy.
This morning, my right hand and foot were tingling, and my right hand was shaking. I took one Lorazepam. 45 minutes later, the tingling and tremors stopped.
I'm hoping the Lyrica will put the brakes on the chronic nerve pain I have had since the spinal fusion, and now the knee replacement.
Visit to Dr G
Nov. 19th, 2018 06:50 pmDr G had some good information. He told me that this can and often does go away as suddenly has it appears. He also said that the best course of action is to medicate the symptoms away for a goodly amount of time. Then slowly reduce, and I mean SLOWLY, the dosage. Try that for one week and if no symptoms show up, reduce dosage again for one week, and if any of the symptoms show up, go back to previous regimen for a few weeks, then reduce again. Repeat as necessary.
Oh, his office personnel were quite pleased at how organized I was. I had downloaded and filled out on my computer the Patient information form. And got a chuckle out of one of my favorite terms for the bathroom.
Here's hoping...
Nov. 18th, 2018 07:45 pmI've been slowly reducing the dosage of my medications. Today, I have only had the one dose for the morning. My leg feels so heavy, twitchy, sore, and not quite under my control. Sometimes it feels like it's right on the verge of seizing up.
No night dose. Not sure if I'll get woken up by a seizure or not. Trying to not think about it.
Tomorrow, as I typed, I see neurologist. I know there are certain things that has triggered an episode, and I know Dr G is going to want to see it up close.
Where to begin
Nov. 4th, 2018 06:29 pmAfter a week of the proscribed medications, I was still having the dystonia seizures. I can't describe how it feels to have your body trying to force itself into geometrical angles where there shouldn't be.
I did what I was instructed to do, I went back to the Emergency Department (why? Because the soonest I could get to see a Neurologists is December 12th)
While waiting to see a doctor, I had a seizure. My son, and a ward nurse were there to help immediately. After waiting another hour, I got to see a doctor. Or should I say he brusquely spoke to me. Then he left, saying he was getting some information for me.
While I was waiting, I was asked if I could move to the ambulatory waiting room, as they were swamped. No problem. Alan and I went there, each of us sitting in a chair waiting. The doctor showed up, and asked us to follow him. I stood up, took three steps and started having another seizure. The 'doctor' saw what was happening, said "Oh, I'll be back when when you're finished." and walked off and left me there, in extreme pain, with my son preventing me from falling to the floor. After the seizure was over, my heart was racing, and I was gasping for air.
The 'doctor' showed up and gestured for us to follow him, and then disappeared again. I presumed he was getting me information.
He was. He handed me a fucking POST-IT note with a web address. And then he just walked away.
Wing and I had a conference call with two friend, filling in some of the details of the useless visit to Fiona Stanley Hospital.
Yes, I had a seizure while waiting to be seen, but I also had another one when the doctor asked me to follow him, and when he saw what was happening, he said "I'll be back when you're done." No offer of assistance, help not even a comment. He just walked off. If it hadn't been for Alan, my son, I would have landed on the floor.
This is NOT acceptable behavior, and Wing, Daryl, and Meegan said I should lodge a complaint.
So, I have lodged a complaint against the 'doctor' that was treating me, watched me having a seizure and said "I'll be back when you're finished'. Person taking the complaint said that behavior was unprofessional and unacceptable.
Complaint has been written up, and filed. Maybe he will learn to be a bit more empathetic.
I still don't feel any better. If anything, emotionally, I feel worse.