I was diagnosed with GAD in 2005. I think everybody's different as far as meds go. SM
Posted By: MissouriMT on 2008-05-20
In Reply to: Have any of you been diagnosed with generalized anxiety disorder? - Your expertise requested
I am on Effexor XR 150 mg a day and it works wonderfully for me, although when I forget to take my pill, I do get that strange dizzy, buzzy feeling that someone below described. I also have Klonopin if I need it. It's not as strong as Xanax, but it takes the edge off and helps with sleep.
I'm curious what was the catalyst for you being diagnosed? I have always been a "worrier" ever since I can remember. I bite my nails, but it was always manageable worrying. Then in the fall of 2005, I had a full blown panic attack. It was the worst experience of my life and I hope that I never have to go through it again. I had a gallbladder attack. I new it was my gallblader. I knew I wasn't have a heart attack and yet it was like one half of my brain could not convince the other half. I started feeling lightheaded, dizzy, and like I was in a tunnel. I was at work and someone told me I should go to the employee health nurse. I did and my BP was through the roof, my pulse was 130, and the nurse just ripped that BP cuff off my arm and said you need to be seen in ER and made sit in a wheelchair and wheeled me down there!
The irony is the more urgent she acted, the worse my panic got. Finally, it was established that I was not having a heart attack, but still my body was freaking out. I could not calm down. Then I started crying and cried for two weeks straight. I couldn't sleep at night. I didn't want to be home alone. I didn't want to go out in public. I just basically sat in my house, on my couch for two weeks straight crying and fretting. My doctor tried me on several different medicines including Lexapro and Zoloft, both did nothing for me but make feel nauseous. Then he wanted to prescribe an antipsychotic which made me freak out even more. Being a medical Transcriptionist and knowing about drugs, side effects, etc. was NOT conducive to my anxiety disorder!
Finally, I found a female nurse practitioner who was wonderful. She new exactly what I was feeling. Told me her daughter had the same issues and started me on Effexor. I have been panic attack free going on three years. I get what I call mini panic attacks where I can feel myself starting to freak out, but I've taught myself relaxation and breath techniques that calm me down.
I'm just jazzed to meet people who have the same "disorder" as me, ya know. When I've described my anxiety and panic attack to my family and friends, they just look at me like I should be committed and when I was going through it, my family didn't have a clue what to do with me or to say to me. They were afraid of me, really. My mom kept saying "you need to snap out of it." Yeah, ma. If only it were that easy!
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I had one in 2005
And I do still have a period, but by far not anything compared to what it was. It's between spotting and a light flow. Some months are worse than others, just like a regular period, but still far better than what I was putting up with. I would strongly consider doing it. My doctor told me that whatever I'm doing at 6 months postop, whether it be bleeding like a regular period or just spotting, that's probably how it would stay forever (or at least til menopause...then I guess we'll see  ), but for now I'm enjoying it! Good luck with whatever you choose!
Tessier is Best and has new 2005 3rd Edition sm
I was delighted just before Christmas to find out Tessier had come out in a new 3rd Edition in 2005. This was always my favorite in the 90's, and since it arrived it is my new favorite now. It is big, 2000 pages, combines material that would be found in 2 Stedman's books, Surgical Equipment AND Surgery Words. I still use my Stedman's specialty books but 95% of the time I find what I'm looking for in this new Tessier.
I do full time Op Reports for a very big teaching hospital, plenty of specialties, and it's all in this book.
I paid $41.95 with free shipping because I used my credit card. They will send you the book and bill you but you would have to pay shipping and handling.
The price is great considering it's the equivalent of two Stedman's books, and I think much better.
You won't be sorry if you give yourself this terrific tool from the start.
Wise
Here's the link to the Elsevier site. You may have to call in to get the free shipping, it may have been a special.
P.S. Don't go to Amazon, they are not selling the new edition.
http://www.us.elsevierhealth.com/product.jsp?isbn=9780721600208
my Pop died early 2005-have never gotten over it
congress passed no law in 2005
Introduction
This article applies to users in the following regions that have experienced daylight saving time (DST) or time zone changes during 2007:
U.S. and Canada (where DST is observed):The U.S. Energy Policy Act of 2005, passed by the U.S. Congress July 2005, extended daylight saving time in the U.S. by approximately four weeks. As a result, beginning in 2007, DST for the U.S. will start three weeks earlier on March 11, 2007, and end one week later on November 4, 2007, resulting in a new DST period that is four weeks longer than previously observed. These four weeks are referred to in this article as the "extended DST period." Visit MSN Encarta for more general information about DST. Canada chose to follow the U.S. change, in regions where DST is observed.
U.S. 2007 change in daylight saving time:
Previously DST started on: With the new law, DST will start on: Previously DST ended on: With the new law, DST will end on:
First Sunday of April Second Sunday of March Last Sunday of October First Sunday of November
Would have been: April 1, 2007 Will now be: March 11, 2007 Would have been: October 28, 2007 Will now be: November 4, 2007
Other regions: Microsoft is providing updates for several other regions or countries that have enacted time zone changes in 2007, including:
Universal had Dr. Suess in March 2005
they also had Nickelodeon. You will definitely want more than one day no matter which places you go to.
Tags $35.00 for 2005 Nissan in Ft. Lauderdale, Fl.
xx
movie was Layer Cake in 2005.....
xx
tubal in 98 reversal in 2002 and baby in 2005
I was in a really bad marriage and knew I wanted no more children in this relationship and so I spoke with my OB/gyn and her performed a tubal not removing any of the tube just cutting and cauterizing. In 2000 my hubbie and I married and he had no biological children so we had my tubal reversed at a cost of about $3000 and little or no discomfort. A couple of years later and some Clomid (because of my age) I gave birth to an almost ten pound baby boy and am planning on working on a little sister currently *~*~*weg*~*~*~
no, was diagnosed 8 yrs ago but have had...
I have had it since my 20s, I remember my LFTs were crazy then, they had no test for this in the 70s-80s. I didn't KNOW I had it. My husband had it (ex) and he was tested in 1992 and many friends had it and all told me to get tested, but I felt/feel like a million bucks so I laughed them off or poo-pooed the issue
In 1998 I decided ok - get tested and my case was so mild that it looked like I was only a *carrier* but on further testing I had it. Last year I went to that GREAT specialist (who really specializes in C and is an older MD-I like that, not *green*) who confirmed my suspicions. My tests are excellent and for decades now, I take care of myself.....and I don't eat raw fish...(my ex did and still does and another MD told me he's nuts to do so), and I will NOT die from it - because I have had it forever....
I also read that online years back......that if you've had it for 30-40 years and doing great, you'll die from something else......but if one continues to drink and drug - well, then, you will die from the disease.
My dad has been diagnosed with
a bacterial infection that is very rare. The word sounds like Narcartia but I am not able to find anything on this bacterial infection so I'm probably spelling it wrong. Does any one have any suggestions or know where I can go to get this info?
He became very sick, had a couple of episodes of losing his sight. When I found out about it (a week later) and he went to the ER, the initial diagnosis was spinal meningitis. This diagnosis eventually "evaporated" for the lack of a better word. CT scan revealed a lesion on the brain. This was not able to be identified. Brain surgery ensued and this biopsy was sent across the nation to multiple labs. One lab finally made an association with "agriculture, ground, farming." About six weeks ago, my dad had spread chicken manure on his garden. What complicates the matter is that he has arthritis and is on Remicade with a depleted immune system. This is probably why this affected him. They are treating him with an antibiotic IV every six hours around the clock. There is only one antibiotic that will treat this bacterial infection. This is making him very sick. The antibiotic does contain sulfa and I don't know that he is allergic to that but I have heard that sulfa medications can make some people very sick.
One other note to help in getting info on this. This must be something that is sometimes seen in AIDS patients because of the depleted immune system. I have tried to Google it in conjunction with AIDS and still cannot come up with info.
That's the story and any info that anyone can help me with would be appreciated!
They are probably diagnosed with
lung cancer because either they had it when they quit or because they are susceptible to it because of the smoking. My dad quit and died 2 years later. Either way something is going to get you. When it is your time, it is your time--that has always been my philosophy.
Anyone diagnosed with shingles and if so
how long had you had before the diagnosis and have you had any complications from it, such as constant pain, etc. Thanks
I have been diagnosed with fibro but
I have fatigue sometimes and don’t know if from that or from the hypothyroidism that I have, double duty so to speak. I have appointment this week to see what exactly is happening with me. Terrible, terrible pain for days on end- thought fibro, now not sure. I have some hydrocodone and take 1/2 pill of that when severe pain with fibro, supposed to start rehab for mild exercises but too much pain involved now with ?? I had a boss 1 time and she said she started exercising and that was the only thing that helped her. I just have had some setbacks to where I have not been able to start yet (including shingles!!). Hurt so much with the fibro and think the shingles started because of that. I can sleep at night, no problem there but some mornings unable to stay in bed because of hurting. I will give a follow up when I visit my physician this week and see what he has to say about if this is fibro, what does he think is problem, things you might do for fibro, etc.
Yes - i've been diagnosed
for many years now - just was not aware of this somatization disorder and its correlation with fibro and CFS. I would skip the rheumatology route and go straight to pain management - you will save yourself a lot of time and money. I live in a large metro area and have access to many very good doctors, but until I went to a pain management group of anesthesiologists, I never got any relief. My internist who I fired kept me on prednisone for 8 years and he actually got mad when I told him I was taking control and going to a PM specialist - that I was tired of him jerking me around and I resented having bought his car and put his kids through private school because of his inability or unwillingness to treat my pain issues. Yes, I am on narcotics - don't let that deter you - they work and not everyone that takes them becomes an addict. My life has been much better since I have been out of pain and am mostly bothered now only by the CFS - which no one has found anything really to help that. I sleep a lot and have learned my limits - I would just really hate for you to waste your time with a rheumatologist - they are for people with arthritis and inflammatory conditions. Fibro is not an inflammatory process and the rheumies don't offer any real treatment for what ails you.
Just reread your post - I would be interested to know what treatment the rheumie has planned for you -
Yes. I was diagnosed 10 years ago
with early stages of cervical cancer. Had a cone biopsy done which showed that the cancer did not spread or in situ. I decided to have a total abdominal hysterectomy, kept my ovaries, because I did not want to go back to the DR. every 3 months for testing and the chance that the cancer could return. No chemo or radiation. I was very lucky.
What makes you think you might have cancer?
Have to get those PAPs every year ladies. This is a very treatable disease.
Has she been formally diagnosed?
I get an outbreak on my nose every now and then, and the doctor prescribes Acyclovir. Don't know if it's the same when it's on the lips. Acyclovir works great, and you can use it either prophylactically and take it every day so you won't get any outbreaks, or you can use it when an outbreak is coming on and it's gone within a day or so, and it never has a chance to get bad. Again, I don't know if the lips are different than outbreaks on other body parts. My husband gets one on his leg and he takes Acyclovir too.
I have been diagnosed with fibro about 9 SM
years ago. You mention the pain is in your ribs. When I was diagnosed that was not one of the key points, of which there are many. I have pain all over, really. I have very much pain in my neck, wrists, elbows, shoulders, lower back, etc. I have terrible burning and pain in my muscles in my arms and legs as well. I have advanced osteoarthritis and chronic fatigue, which can also accompany fibromyalgia, as I am sure you know. Symptoms can certainly vary from one patient to another. I wish you luck and success in your efforts to control pain. I wish I had the answer for everyone suffering daily with chronic pain.
Anyone here diagnosed with Lupus?
I've been getting worse and worse physically and am in the process of being ruled out for all sort of stuff and this (Lupus) is one of them...some test came back positive but it's not definitive and I may have to see a specialist. I should really pay more attention but it's so hard to focus when a bazillion things are racing through your head while you're sitting nekkid freezing your hiney off on a paper-lined table.
So, yeah, anyone got this disease and, if so, how are you dealing with it? I'm just bummed out with the amount of pain and fatigue I have. I mean, I'm all crippled up and can't even sit here at my desk for more than an hour at a time anymore and chores that used to take 20 minutes or so now take up to 2 hours. I actually was so exhausted and in so much pain I curled up in a ball on my living room floor in front of the wood stove and slept for almost 2 hours before my husband found me and got me up on my feet. I'm only 35 and this just ain't right! Any advice is much appreciated.
While I've never been diagnosed with
lupus, I sometimes think I do, but when my rationale kicks in, I realize it is the wear and tear my body has taken over the past 40+ years, in addition to overwhelming perennial stress. Stress can cause lots of symtoms that mimic other diagnoses.
I do wish you the best and hope you get to the bottom of it and feel better. You are a delight to have on this Board.
she's been diagnosed as bipolar
of course, that's according to the press.
My dad is bipolar and has s/a and alcohol problem. I know how heart breaking that can be. It's like people who overeat. We all feel sorry for fat people but if you chose drugs then you are such a bad person but it's the same thing, really. A compulsion is a compulsion, no matter what you are taking into your body.
Diagnosed with this since the late 80s,
in fact I went in and told the doctor what to check for, had the classic symptoms, intense itching (waking me at night with urge to scratch), terrible coldness all the time, having to sit under blankets. Mine now has turned into Hashimoto's thyroiditis, I was told just a few months ago, thyroid totally gone. Now with the Synthroid, I told my physician did not want to take any more, loss of hair really bad, heard Synthroid noted for that. I asked and now on Armour thyroid and seems like loss is not as bad but still some. People on here have posted against Synthroid.
I was diagnosed 11 years ago and that along with SM
other physical conditions is why I cannot do a full day. I support myself and still have to do it without benefits, etc. I have tried different things for pain, but they either upset my stomach or were even taken off the market. I know exactly what you are going through. Sometimes I feel so bad I can't even put it into words. Good luck to you.
some people never get diagnosed at all because they
x
i was just diagnosed with diabetes
No insurance. Went to the doc yesterday to go over lab work I had done in November. My blood glucose was 127 (upper limit of normal being 126). I am 45 yeard old and overweight, but I never had this happen before. He then did a glucometer reading (after I had had three cups of coffee, each with two sugars, of which I was still sipping on as he took the reading). He then ordered new lab work as a recheck, but stated he had to put NIDDM as a diagnosis on the requisition form. I don't feel a diagnosis can be made that simply. What's really upsetting is the fact that he informed me that now since I had been diagnosed with NIDDM that I would probably never be able to get health insurance with a pre-existing condition such as this. I feel that through correct diet and exercise over the next few months I can easily lose ten or more pounds, and that this more than likely will change the status of my next lab values. I feel so very sad about this. What do I do??
My mother was diagnosed back in her 40's..
Hers came on after a stressful injury, as I've read this tends to come on after a very stressful situation, injury, or illness, and she got progressively worse. She hurt all over, was so tired she could barely move, was trying to work while this was going on and it was about to make her crazy. There would be days she would cry she hurt so bad all over and then would fall asleep into exhaustion. This did go on for several years and then began going away little by little. She just has a flare now and then, but mostly under stressful situations. My doctor did tell her that she should continue to exercise, force herself to do what she can, and then she definitely needed to rest, get enough sleep, eat a proper diet. He said there could be a day or two flare, weeks of a flare, or years, as in her case.
To answer your question, she did get much better and doesn't hurt all over all the time. She was just so tired she couldn't function, which I had never seen in her before.
I have been diagnosed wth fibro about 10 years ago SM
and know what you are going through. I read somewhere that it is impossible do describe the pain, and that is how I feel. It is a gnawing, pulling, burning, aching, fatigue all the time. No one has helped, and what meds I have tried gave too many other bad side effects, stomach upset, etc.
My daughter was diagnosed with ADD in 2nd grade
We took her to 3 different doctors who did a bunch of different tests and all three said without a doubt she has ADD (without hyperactivity). So, we put her on medication. The medication made her VERY cranky and she was a holy terror to live with!!! So, we went back to the doctor and he switched her medication. This medication made her mood better, but her appetite was virtually nonexistant. My husband and I read every book and website we could find on ADD to see if we could help our daughter. We ended up taking her off the medication and changed her diet, making sure she eats every 2-3 hours. We eat pretty healthy anyway, but we really have to make sure that we don't let her eat too many carbs or junk. She also has to eat pretty frequently to keep her attention span up. It has been 2 years now and she is doing great at home and at school. She just started a new school this year and this teacher is excellent at letting the kids have a healthy snack during class so the kids stay focused all day long.
In other words, before you even think about medication, I would monitor his diet and make sure that he's eating healthy and then make sure he's eating every 2-3 hours (if possible at school) and see if this helps.
Adult ADD? Never diagnosed but wondering (sm)
So all my life I have been disorganized, first it was papers hanging out everywhere from my notebook, now it is everything in the world stuffed in my purse. My mind wanders all the time. I do transcription but flip back and fourth between here and my work and my e-mail and other things on the net that interest me. And i have to have background noise while I do all this. My house gets very cluttered and than I have to work like a maniac to get it cleaned up but still things are kind of in haphazard places, not really organized. I just always feel overly busy, overly tired, and behind on everything. So....could I have ADD? Or am I just too busy, bored with sitting in front of the computer, and disorganized??
I had a "slow Mohs" in 12/00 after being diagnosed sm
with melanoma in situ on my left cheek near my eye. I had about 8 shots and I didn't feel a thing. I guess it was called a slow Mohs' because the procedure was about 4 hours long. The wound was open for 1 week until results came back that he got it all out. So for a week I was doped up, as I had a hole in my face that I could put my finger in. I barely have a scar there, he did an excellent job. And so far, no return of the cancer.
My cat was just diagnosed with lymphoma last night.
She is 10 years old. I noticed that her back hind leg looked very swollen last Friday. When I felt it, it was a huge lump. She has not been eating and not drinking any water at all. I think it has been there a long time and just did not notice it until last Friday. I was given the option of amputating her leg, which I cannot do. Give her prednisone and start chemotherapy, but how much time will that give her? She looks so sad and sleeps all day and it not using the litter box, about once a day.
I had to make a very hard decision this morning, and I am having her put to sleep. It makes me so very sad, but I do not want her to suffer. I am going to bring her home today and place her to rest in my garden under a park bench I have out back. I could not think to just leave her there. I am going to miss her greatly.
Just needed to talk as I have been crying all morning and trying to work. I am not going to get much done.
HIV meds
My best friend has had HIV since 1993 and is very healthy otherwise. He was taking many medications but about 3 years ago the doctors did his blood counts and said the disease was virtually undetectable. They advised him to quit taking the meds and see how it goes. They told him the meds lose efficacy after awhile and so did not want him using them until he actually needed them. After 3 years off meds, his counts are still doing great. I wouldn't worry as long as she is still having regular check ups with the doctor and otherwise maintaining a healthy lifestyle.
BP meds (sm)
When my husband started a medication for BP he started having strong muscle twitching he'd never had before. I think it was something odd, like his pec or abdominal muscles, but I can't remember. The MD had just started him on 3 new meds, one of them being a BP med. That's the one I suspected, and sure enough, muscle twitching was a possible side effect, especially if the patient exerted himself and perspired a lot. I think it could cause potassium depletion and that was the reason for the twitching.
My lab was diagnosed with an allergy to pine needles and had the same
symptoms you are describing. Now, I live in North Carolina where pine trees are as common as grits, so I thought the poor things was doomed!! My vet suggested a cortisone injection in the early part of the season before it got to really take off and then 2 tablets of Benadryl twice daily, which seems to have worked great for the past 6 years, but if I delay that darn shot and she starts that itching then I run into problems because not only is she itching from the allergy, but from the irritation caused from the scratching.
I studied the disease back in 98 when diagnosed
and thank goodness for the web!!! I continually get educated all the time from being online. I love it. Glad you're feeling well!!!! Attitude has much to do with it.....
Hope you aren't diagnosed with fibro
because no one believes you anyway. I had heard about before, did not know really much about, if I typed on it paid no attention, diagnosed in 2004 and not having fun yet. This is so far uncontrollable for me-mine might have been better controlled if diagnosed with rheumatism- I would suppose rheumatism feels a lot better than being over the entire body.
Have any of you been diagnosed with generalized anxiety disorder?
I have within the last week or so. Just wondering what meds your doc put you in and if it is helping and how long it helped all of your symptoms. I guess I was expecting "a feel-good feeling", too, but not really. The anxiety is definitely better. Had gone to the ER 3 times in less than a week, thinking it was my heart, but not.
Any help would be appreciated.
My husband diagnosed 1 time with diabetes, get this
he ran 1 high blood sugar and was diagnosed. He did have elevated blood pressure but for years and years controlled his blood sugar and the elevation was always and I mean always low- the insurance company would NOT cover him because of that 1 only diagnosis. I tried talking to them- they told me 2 counts against him- unable to get life insurance on him. This diagnosis was made on a job entry and for 7 years he kept his blood sugar average or below, made no difference. I have been there.
I read MRSA first diagnosed in 1961
There are things that unless you pick them up, may never know. I have an example: Had carotid ultrasound done. I asked for and got the report (I save any and all that I can including lab work) and the neurologist said ok. Well, happened to have 50% stenosis of the left carotid artery. I asked is that a concern to you and he said well, it should be watched ever so often. Another time, going to have elective surgery done, got EKG and lab done ahead for that. The EKG read abnormal (this was one I was picking up from a previous appendectomy surgery I had). I then asked my internist about it. Never mentioned to me at all. Needless to say when I see abnormal on something, only surgery is a have to surgery, not elective. I see mistakes all the time on my records, not sent out but diagnosis for a scan- had it showing me having hypotension and I have hypertension. Even when the people in the office doing the click and go reports before seeing the doctor, have found errors there. These are not outsourced reports, done right here in the USA. I always get copies of everything.
I don't think the depression meds --sm
should be taken in conjunction with pot. Anger and anxiety issues were already present prior to father's death. He may be grieving on some level, as his own psyche will allow, but sounds more like an excuse to me. I have lived with these types in the past. His lack of ambition is probably due to the pot, as well. Thinking of the child, I feel that separation from the source of this frustration would be the best thing for the boy. Counseling rarely works for the spouse, but it would probably benefit you. Go with your gut reaction on this as to what is best. You live with the man, and you know more about him than what you can post here. Trust your instincts. Good luck to you.
Fibro meds
I was diagnosed in January of this year by a rheumatologist after having problems starting last August that began with a rash and my GP did a battery of tests - the rheumatologist started me on 1500 mg of Relafen (which has greatly diminished the tender areas like my hip areas), I also take 150 mg of Zoloft, 600 mg of neurontin, 50 mg of Tramadol every 4 hours as needed (which do me has not really helped the pain 100%, but it does lessen it a good bit) and I take a muscle relaxer at bedtime and sometimes during the time. These meds do not zap me and I feel more functional with them than before. I also take Halcion if I am unable to fall asleep, however, these days it seems that I am so exhausted that I have no problem sleeping as long as I am not hurting and the muscle relaxer at bedtime seems to help with that. Of course now that my inflammatory markers are at a near normal range I am walking 30 minutes a day and have begun stretching exercises 15 minutes in the morning, 15 minutes at night to help with the muscles. The rheumatologist has said that all of these will change as the fibro progresses and I age (I'm only 33) but he said if we stay on top of it it should be very tolerable for me from now on - I am thankful to my GP for the referral to this doctor because I have read of so many stories where the GP ignored the patient's complaints only putting them on powerful pain meds and not really getting to the source of the problem or telling them that there is nothing wrong or nothing they can do...I feel now that the pain is being managed, my biggest complaint is being tired at doing the simplest of things - like folding clothes - I feel that I need to rest after I do that - whereas before it was just a normal thing. My rheumatologist has stressed that sleep/rest is very important so he says when your body tells you to stop and rest - do it - whatever it is you have on your to do list can wait - otherwise you're gonna really feel bad and then nothing on your to do list will get done. I see my rheumatologist every 3 months right now and he says once I am doing okay on the meds and everything seems in check we'll go to every 6 months and then yearly until something goes out of whack and my treatment needs changing - he seems to really be on top of things.
What meds are you taking? Do you see a doctor on a regular basis?
Needing meds
I think just the opposite - it's the rest of you who could use the meds - or at least not be so judgemental - but I have found that this board - regardless of the subject has quite a few very rude, mean and just downright B***tchy women - sorry if you were offended, but it was my right to BF as long as I chose - and until you work hard enough to get a law passed against it - it's something you must deal with - I think that most of you are jealous of the fact that this is not something that you could do - or wanted to do - maybe you are feeling jealous because my kids are great - we have great relationships and maybe your kids don't even speak to you unless they need money - Most of you would give anything to have a family as close and functional as mine. However, it is something that you will never know. God has been very good to us - and thankfully I followed his Word and not yours.
Thanks - have been seeing a psychiatrist for meds
After a couple of years or so on the same meds, they stop being as effective. That's why we're trying Cymbalta.
I am more cyclothymic than bipolar (rapidly cycling, less extreme mood swings). I tend toward the depressive end of the scale most of the time. The Cymbalta did trigger my hypomania - but I'm hoping once my body gets used to it, it will keep me on the higher end of the scale but not as far as hypomania.
I'm going to give it a while longer to see what happens. Many thanks to all who responded!
No advice about meds, but...
if you are consuming caffeine, try cutting back. It helped me significantly. Even 1 cup of coffee was aggravating my anxiety.
I was on three meds before finding the right one (sm)
Zoloft made me too sleepy, Effexor didn't do much but gave me strange buzzing sensations when stopping it. Prozac, low dose (10 mg a day) has helped a lot. I take it in the a.m. so it doesn't keep me up at night. But by the end of the day it helps me sleep. (I also take melatonin for sleep). At first you may have some palpitations when your body is getting used to the Prozac, not sure about the other meds with that symptom. I definitely think Prozac is the best.
cholesterol meds sm
I was given Tricor (expensive) and it gives me embarrassing gas, only take it when I'm going to be alone, so it wasn't powerful enough and they added simvastatin which they told me to take before bed because supposedly that's when the cholesterol is best treated by this. I found it kept me awake or ? psychological??? I tried to stick to it because I have a doc's appt. Mon. and was so tired and nauseous from taking both, I actually feel like I have the flu. I think I am going to express the desire to just try diet but know I'll catch He*l, as they seem to prefer you to take all this stuff. I never heard of statin shuffle, can't find it, that's awful! Last time my #s were down to normal and they were so excited, well, now I think it's my turn to start to live again. If you can take it with no side effects, then do it, but I'm sick of feeling sick. Both parents had and died of heart disease, so I'm scared. There has to be a better way!
There are some Club Meds that do not
admit anyone under a certain age. Not all are family friendly, some very adult themed.
noncovered meds
Yes... This has happened more in the last 2 years than it has in my other 40!
I asked for birth control about a year ago and chose "the patch". My insurance company didn't cover that, so I decided to go with Depo Provera. Guess what... they didn't pay for that either.... LOL
I was diagnosed with fibro but the rib pain, front and back
started 2 years ago when I got back from vacation and has been there off and on since. Sometimes horrible pain, sometimes just there but never completely gone. I went for 1 acupuncture but it is $70.00 out of pocket for each treatment, insurance does not pay so instead I am doing the 70% chocolate, 2 pieces a day because read that might help because of the antioxidants and flavinoids. As long as I am not touched anywhere around the ribs do pretty good. Have tried the chocolate for a week now, cancelling doctor appointment this Tuesday and will see if that holds the pain. The chocolate lot less costly than the treatments. I have found absolutely no assistance with any physician I have gone to, none including pain specialists, rheumatologists, ortho, etc. I sometimes have extreme fatigue, can lie down for a while and it seems to go away. I have hurt all over with the fibro but now my pain issues are the ribs (oh, forgot about the feet but too long story on that). Did your physician give you anything for the costo? I do not take anything for the fibro nor the costo. I had to dust my fatcat today and I thought she weighed a lot, she is only 20 but still had to pick her behind up and put her in the bathtub.
I commend you for that...I am on Rx pain meds
and on 4 per day or every 6 hours. After doing this for a couple of years, I feel it is time to stop even if it means having to have surgery down the road. If I take even 1 less pill a day I feel the anxiety you mention among many other very unpleasant symptoms if I take less than that (clammy, achy, etc.) How many pills were you taking? And how did you do it?
Can you name 3 meds that don't come with scary waringing?
x
Did you know that vaginal yeast meds
and many of the meds for jock itch, ring worm and athletes' foot are the same exact drug? Now the sprays and/or powders use different ones from some of the creams, but the some of the athlete's creams are just like some of the vaginal yeast creams. It's all for fungal infections, but the makers want you to buy 3 or more tubes please, LOL.
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