Anyway, when I took it to the pharmacy, all of the medications was controlled substances, percocet, sonata, and diclofenac. I was shcoked but the pharmacist tech already scanned it and I trust the FNP. I always go to this same pharmacy and never had a problem filling my prescriptions and my disabled problem. The pharmacist was even willing to fill the diclofenac at the time. I decline and told her I would pick them up Monday when all 3 were ready and I this didn't fill right.
I've searched the web and here and no really good answer. I'm taking a Sonata about 3 or 4 oclock in the morning. It does cause some jitters next day. Now I've started Sam-e and a Super Beta Complex and the Jitters are unbearable. I take some Xanax and it helps some. I can't take much and still function.
The question is ... Is it the Sam-e or the Super B Complex causing the extreme jitters or anxiety?
There really aren't very many specialists in the area of dysautonomia, I'm afraid.
I was told P.O.T.S. could be hereditary and later learned I have a second cousin who has been diagnosed with the same thing. I've not had any official testing to determine the underlying cause of my autonomic dysfunction. I was diagnosed with P.O.T.S. back in 2004.
It's official! Got my lab results today: 24 weeks EOT undetected. Thank you Gillead, this forum, my Dr and his coordinator!
To summarize, I was genotype 2a, infected in 1995, took Sovaldi + ribavirin for 12 weeks starting in May 2014 and was undetectable since 4 weeks into treatment. This was my first and only treatment.
Viral load was 7 million just before the treatment and 16 million 2 months prior. All liver enzymes were always in the middle of normal and platelet counts 215-250.
Ohhh well thank you very much.
Anyway I have been with this replaced doctor for a yr and a half, I had been explaining to him that 2 vicaprofen in a 24 hour period is not sufficient he by the way had taken me off the motrin and changed my Xanax to Ativan. I also have been on sonata 10 mg for all these yrs. I was given a urine test which is pretty normal, before I took it I told him that there would prob. not be hydrocodone in it as we had been discussing that I needed more pain relief.
Of course, as a Gt 3 I must keep in mind what Hector posted on another site, this week about the study of tx follow-up where out of 863 people 85 relapsed and 83 of those did so before Week 12. Two relapsed AFTER Week 12 and they were both Gt3s.
However I am thanking God for the blessing of SVR 12 and am going to be aware of the possibility, but not stress over it. My Dr has already given me the paperwork for Labs end of May for a June appt.
Well, it's official. I received my diagnosis today. I was getting a EMG and while I was in there my neuro busted in and filled me in. I also have arthritis in my spine. Awesomesauce! :-/ I am supposed to start a 3-5 day IV treatment of steroids and I think they gave me homework? I have a butt load of stuff to read about MS and medications and then in a month I go back for another appointment and decide what I want to take. Why do they all of the meds have to be injectable!?
I have a real problem with insomnia I went to the doctor last week and got Sonata for sleep and I asked for clonadine because I knew that I would be out of pills this week and would be having w/d sysptoms. He did not want to give me that he gave me klonapin instead.. I have not told him I have a problem with pills. The sonata is not working for my insomnia so I have made an another appt to see him this week to see if I can get the clonadine.
I'm a diver and twenty I landed really hard in the water off a 3m board on the side of my face. immediately at impact I could hear ringing and my hearing was blocked. it sounded as if you but a seashell on top of your ear ad the hearing was just muffled. I can still hear by It isn't as good as my other ear, everyone said it was just eternal but after one night of sleeping on one side is still there. any clue on what it is? and if it's serious?
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