Mild dose symptoms and conditions

I was on 5/10 lotrel, a mild dose over 3 months. I took myself off of the drug and learned to relax more, and have a better diet and exercise more. I felt weird where I could not focus on my priorities, and the way the medication made me feel made me think of it more than I wanted to rather than life. I am normally a no headache person. While on the medication, i had horrible headaches where I had to take Excedrin migraine to get over it. My skin after taking it for awhile became dry and itchy. I had dark circles under my eyes, which was new. My knees and feet and hands became ice cold. I think it is because I believe that my blood pressure the way it was, was what my body needed, and maybe there was not enough circulation with the very low 117/60. My normal and feel good blood pressure is about 140/85. I am happy with that and will keep it. Also wild at normal 140/85 my blood sugar is normal. when I took the medication and it dropped to 117/60, my blood glucose rose. My body was releasing glucose because it was saying, hey something is not okay here. I think the drugs are bad, and now I eat organic vegetables, no coffee, no sugar, protein meats, and soy milk, unsweetened almond milk, walnuts, blueberries, whole grains. No white bread, no sugar, no soda, no fried food, no white potatoes, no white rice. My range is now 120/70 to 140/85 when i am rushing around. That is normal. I think medications change your body chemistry. When my skin became itchy and my extremities cold, and my body started shaking and freezing and sweating, it was from the pills. if you want to know you readings, don't go to the doctor. Buy a self test BP machine, Glucose reader, cholesterol meter. My doctors cholesterol count was 100 over another text i had at a free clinic. Maybe they cheat the numbers, who knows, to make you think you are sick and bring you back. take care of yourself, and get away from the fear and panic the doctors put you in. you are way better to see a natural nutritionist if you need help. Break a sweat every day!...that will help.

I had Mirena inserted in 2007 due to a lack of tolerance to birth control pills. The experience was very painful for me. However, the doctor explained that the initial insertion process is different for every woman as we are not all designed the same. My cervix/uterus is oddly positioned. According to the doctor they are "crooked". As a result, the doctor had a difficult time properly inserting the mirena, which in turn resulted in major pain! But, this was just my personal experience. Not every woman will encounter this difficulty. However, I would recommend taking at least 2 ibuprofen before the procedure. Throughout the past 2 years, I have experienced a range of symptoms. Major depression, severe mood swings, acne, lack of energy, excruciating lower back pain which mocked mild labor pains, and the overall inability to function normally. I begged the Doctor to remove the Mirena 6 months ago, but she convinced me otherwise considering I cannot tolerate birth control pills either. Nevertheless, I am 35 years old, have one child already, and do not plan on having more. Well, last week, I was basically confined to my bed due to excruciating lower back pain, and severe bleeding. I called the Doctor, and they finally saw me today. I insisted on having the Mirena removed once and for all, and already feel 100% better just 12 hours later! The purpose of my message is not to discourage anyone, as we all have different levels of tolerance when it comes to pain, medications, etc.....Yet, I felt compelled to share my personal experience as it was not a positive one for me! The only "positive" symptom I obtained from the Mirena was a lack of periods. Unfortunately, there was a downfall to that as well. Due to a lack of a regular menstrual cycle, I felt extremely bloated, and had difficulty losing weight despite working out 5 days a week, and eating a proper diet. I sympathize with each and every one of you, and appreciate your efforts in sharing your experiences. Upon stumbling upon this website a few days ago, I finally found the courage to have this thing removed so I can once again "feel normal!" Good luck to all of you!

As I read all of these postings, I see I'm not alone in my side effects while taking lamictal. I started out on a very low dose (12.5 mg) and doubled this amount each week. It took a while to get to my current dosage of 150 mg per night. I've been experiencing mental confusion, more panic attacks and it's very hard to wake up in the morning. I've been more frequently tired and dizzy during the daytime. Also, at night, my dreams have been extremely vivid. Many have been nightmares leaving me in a state of severe confusion as I try to awake in the morning. Recently, I started having upper back pain that I've never experienced before.
I thought this drug was supposed to be safe with very little side effects (except the potential RASH). I think my life was better before lamictal. Or, do I need to give it some time to work???? Help Please

I don't have a new side affect with Prednisone but just want to share my feelings. I was diagnosed with Temporal Arthritis since last July 2007. I started taking 60 mg of Prednisone for 1 month. Didn't notice the side affects then. Weaned myself off through my doctor's instructions. But relapse occurred when I was only on 2 daily. With Temporal Arthritis, you get delibating and horrendous head pain which is caused due to inflammation of the main artery in the temple. I am back to 3 daily.
Besides my moon face, I am bigger. I really don't have a lot of the other side affects you all talk about. I am sorry you all have to go through that.
My depression is better. My sleep is horrible. Now I am going to a sleep study to see if I have Sleep Apnea.
I consider Prednisone a wonder drug. Although the side affects are horrible, I have to admit, I feel much better, most of the time. I do have inflammation in the neck. Not sure if that is pred or temporal arthritis, but am seeing a rheumatologist for that.

Teena