s ability to learn how to adapt to stress and interfere with REM sleep, and of course are addictive with quite a withdrawal kick. Although you only used it for a short time, people are different in how they respond to quitting -- it should be done gradually even after short term use if that use was continuous as opposed to as-needed occasional use. Don't know anything about Sonata, but all sleeping pills can be habit forming.
It's 8 in the morning and I did not take the Sonata last nite. A little jittery but not much. I think I will leave off all of it l off and see how it goes.
Not much can be worse than the constant jitters.
Nobody officially accused me of forging but the pharmacist looked at me like I was a criminal and the doc never verified the script as of Mon. I didn't want to deal with them anymore so on Monday I told the pharmacist that I cancel 2 of the prescriptions on Sunday and if she didnt get the memo then, here it is again "Cancel all 3 prescriptions now". They put a label on it and I tored the script in front of her face and walked out.
ve taken a tic tac - but there are nights when nothing short of getting hit over the head with a hammer is going to help me sleep! I used to be on the CR version of the Ambien, until my insurance decided it wasn't going to cover that formula any longer, so now I'm back to the 10mg dose. I did find that the CR formula worked better for me, so am hoping my insurance will decide to cover it again soon.
I hope it's not a death sentence! I am a genotype 1a grade 3 stage 3/4. By 26 weeks I still hadn't reached undetectable, so 3 diferent Dr.s in 3 different hospitals said STOP treatment. And I did back in November. I was on weekly doses of procrit too. Well today I am feeling 98% better. I also have NASH. I know this is a silent disease, but worrying about it will not make it better.
I had my Gallbladder remove on April 24 2011. I had been having pain in the stomach area at least a year before. The surgeon said he did not find anything, so he checked my gallbladder and found stones. I expected to have pain from the surgery, but not experience pain all the time..I went to my doctor this week, and he said the pain could last up to a year or more. It hurts all the time, but if I eat any food or take any medication I can feel the pain as soon as I swallow.
I have been on several blood pressure medicines, hydrochlorthiazide, vicoprofen, Xanax, motrin 800, for those 13 years. Since my doctor retired I had to find a new doctor in my area of which I did, he left after 1 yr of which he was replaced by a diff. doctor at the office, I stayed there. I also have hypo thyroid disease.
Again exposure to air would have rendered the virus ineffective to infect.
In an adult, the only way you get infected by HIV is by having unprotected vaginal and/or anal sex by sharing iv needles with other iv drug users. If you don't do any of these, then you are HIV risk free.
My Dr has me on Sinequan. Sinequan for sleep???? It isnt even helping the anxiety attacks let a long putting me to sleep. And everytime I go back for appt they just increase the dose.
Why cant they give me a real sleeping pill like Sonata??
I am very frustrated and getting pretty crabby cause Im soooo sleepy!! I dont even want to be around myself right now let along others.
Sorry that I'm not a native English speaker.I have a conprehension problem on the sentence“HIV is a fragile virus so hard to catch although once in your system it is impossible to get rid of - just the opposite of a cold.”Can you explain it for me in an easier way?Sorry for wasting your time.
I get up and do something quietly in another part of the house so I do not disturb anyone else. I read or balance the check book, or put in a load of clothes in the washer. Or go online and e-mail my friends and relatives. I have the freedom of going back to bed later when I am able to fall asleep. My life has changed and will not be as it was before. I can't have that life back. So I try to adapt and accept the circumstances of this one.
No it's not a death sentence! I got Covid in early 2020. The original version before all the mutations. I was 66 years old when I got it and I suffer from migraine and IBS with some heart arrythmias. None of those conditions are life threatening though, I admit. But basically I wasn't feeling too great before I got Covid. I got an intense feeling of being unwell at first (slight nausea.
Bear in mind that a lot of what you read on the internet is written by people who are not satisfied with their treatment and are not textbook cases (virtually all of us on this forum). People who have good doctors and take their pill once a day and feel well don't get on forums to brag about how great they feel.
I have Hashi's, too. I think you're overreacting.
Simply put, CHF, by itself, is not a death sentence. However, uncontrolled symptoms can be. CHF basically means your heart isn't able to pump enough blood to remove the fluids from your body.
I have had CHF for about 3 1/2 years, and the most dangerous symptom of all seems to be fluid retention. Mainly because the disease is notorious for filling the lungs with fluid, making it hard to breathe.
I feel like I have been given a death sentence. That my life goals are shot because I will not find a man who will accept me and want to be with me after he hears what I have. I know if I would have known I would not have slept with him. Not yet at least. I just want to crawl in a hole and disappear.
Does this get better? Will I be alone for the rest of my life? And no, I don't want to join a "dating with herpes" website.
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