Tina symptoms and conditions

I started taking Doxycycline Hyclate 100mg on oct 25,2009. I have had anxiety, its been something i have been battling with up until 2 years ago and since then i have had no anxiety attacks. When i started taking the doxycycline, i started to become anxious and starting having anxiety once again. I have also become very shaky, i have a hard time swallowing pills so i brake the capsule open and put it my cup, put just a little bit of water in there and mix it around. could this affect the way the medicine is suppose to work. i have no other option because i have to take it to clear my infection, but i don't want it to harm me. please email me at ****** if you can help.

I was reading your post and had to reply to it!! I have been on toprol xl for about 10 years or a lil longer! Started out at 100mg a day now take 200 mg a day. Am a 37 year old female,feeling like a 90 year old female! For the past 3 years or so experiencing numbness started in my toes, now my left foot to right below my knee is completely numb,right foot and leg getting that way!My hands stay real tingly also! When they are not numb they hurt me so bad. I just couldn't believe your post when I read it! Been to neuro telling me I have severe nerve damage in arms legs and feet? I am like from what? Had all kinds of tests and MRI, nothing.... Thank you for your post,printing it out and taking it to my doc! Maybe we have finally got a diagnosis!!! Sounds like it is the meds to me,Not to mention I am also on 3 other bp meds! Just scared me saying I might have M.S. More like toprol xl huh? How is your numbness now? Was wondering if u experience pain w/ the numbness? Thanx T.

My daughter had her 2nd shot in August, 2008, she started having problems November 10, 2008.Since then, she passes out at least 5 to 6 times a month, she has Bradycardia, arythmias, vagal vasal syncope, and Heart Block. She has been in and out of hospitals. The only answer to fix this is a Pace Maker. Shes 18 years old, cannot drive, go onto college (at this time). She could not even go to her graduation ceremony because she was passed out in the bathroom and wouldn't wake up. I cannot find one doctor to connect this to Gardasil, I wonder why it cannot be traced back to the shot. I would love to voice my opinion to the public about her experience since this shot. Out of all the doctors that see her, not a single one can explain why this is happening to her heart, they say she is a difficult but interesting case.

I don't know where to begin; I have a text box in front of me that says "add a new side effect of the Mirena" but all I see are the same side effects over and over. That, in itself, speakes volumes. As for myself, it's been depression, weight gain, exhaustion and yet unable to sleep, pain down to my knees - of course all of these symptoms can be explained by everything else in the world - who, these days doesn't have money problems, stress, employment fragility, etc.? But I know myself, and this is wrong.

I had mine put in March 2009 and after a month I told my doctor I wanted it out. She said I didn't give it enough time (apparently six months is the magic number).

It's now been three months and getting out of bed is an act of heroism for me. Sex is out of the question (well, we have given it a go a couple of times and he can indeed feel the strings, contrary to what I was told - perhaps it's because he's - er - oh, never mind.)

I bleed erratically and it stinks; if I hadn't lost my sex drive already I'd be put off just by that.

I got the thing not for birth control but for pain and bleeding (not that it makes a difference)- it has made the pain worse, so I don't understand why I'm so nervous about asking my doctor (tomorrow - Monday) to have it removed?

I was on nuvaring for about 1.5 years until I quit late summer/early fall of 2008. I'm 25 and I quit because I always felt "dry" and had no sex drive. I felt like I was just pumped full of hormones and wanted to give my body a break and quit all birth control for a while. Around the time I quit, I began to bleed during sex. Not every time, just "hit and miss", not very much, but one time there was quite a bit. I ignored this for a while and then started looking things up on the net which lead me to freak and think I had cervical cancer. I rushed in for a pap test and even during the exam, I bled (pretty badly) this made my results inconclusive and I have to go back in 3 months after the cells on my cervix have re-grown and they can get a proper sample. I'm less worried after finding this forum, but wondering how many others out there have suffered from the mysterious bleeding during sex? Is anyone still suffering from this after discontinuing use?

Other side affects were weight gain, panic attacks, and major hair loss.

Just to let most of you know, that Kenalog will only last several days to a month, if you continue to have symptoms, you need to see your doctor. If you receive kenalog inject frequently then the symptoms and side effects may continue, not letting your body rid of it before your next dose. You should always ask your healthcare provider what it is that you are about to receive, and what the side effects are, it is also up to you to make your healthcare choices, become informed. And never let anyone give you a steroid inject in your arm, unless its for your joints, thats why they are given in the gluteus muscle, because it can cause indentations, and the arms are more seen than the buttocks.

i just started taking itr about a week or so ago i too have had extreme night sweats increased appetite but am definitely sleeping better i,m taking half a tab per night one night i took 2 full tabs because i woke an hr after falling asleep and was sooooooooo hungry just couldn't get full ate at least 7 times in 1 day mostly junk food Tina

My doctor added Lantus to my medicine regimen including Byetta 10, Metformin 1500 twice a day. On the Byetta I lost 35-40 lbs very easily. The moment I added the Lantus I was bloated and over a 2 months I had gained back all the weight I had just lost. When I asked my Doctor about the bloating and weight gain she said she didn't think it had anything to do with the Lantus. But I was losing weight until she added the Lantus! I don't think that's just a coincidence. What should I do? Should I go to a doctor who specializes in diabetes instead of my family doctor who I love dearly?

Stay away from Prednisone

My prayers to all of you who take these destructive "medications". here's my short story.

I had been diagnosed with Sarcoidosis back in 2003. My doctor gave me 60MG per day (three 20 MG tabs) for over six months, with the weening off period lasting another six. To make a long story shorter. I went through many of the same problems like, bloating in the face and body, rashes, a bump that looks like a wart--that still won't go away, and a continuing state of memory loss. I get baffled easy now. I also continue to go through mood swings.

But here's the kicker, I haven't taken Prednisone for over 3 years and I was trying to begin lifting weights. I thought I popped something in my arm, but the doctor says that I have "aseptic necrosis", that has developed in my left shoulder and soon to start in both sides of my hips. For those who don't want to "google" the term, basically parts of my shoulder and hip bones are not getting blood flow and are dying (necrosis).

With my memory loss, I am having difficulties performing at work and doing routine tasks at home. I did not think this "medication" would have affected me this much.

Prednisone needs to be on the banned list of medicines.

Hello everyone,

My name is Tina and I am a mother of 5 children and I was diagnosed with a very rare disorder called "VKH" It is a rare eye disorder that only strikes like 1 in 1,000,000,000 people. I was put on Prednisone to help with this condition and to reduce the swelling in my eyes. I was put on 70mg initially and was tapered down to 40mg. then things did not go as well as to be expected and I was bumped back up to 60mg. I am so happy to read these stories but also saddened at the same time. I have been on Prednisone for 5 months and have gained 20 pounds and have the moon face, the acne, the hair growth and the horrible mood swings. My husband and I had our 10 year anniversary last week and I spent it all alone because of my moods.......
It has destroyed my relationships and my self esteem. I don't like leaving the house barely because I hate how I look and I am so depressed I am not the same person as before. I cry all the time because sometimes I wonder if taking this drug is worth it!!! What makes things worse is I wonder if things will ever go back to normal for me or my family again.................

I'm a 22 year old who was diagnosed with dermatologists a couple months ago. I've been on different doses of steroids ranging from 5mg to 60mg for 5 months now. i was on 60mg the longest and just went down to 40mg. i go down to 30 mg next month. so far my side effects are moon face, swollen areas around my neck and collar bone, weight gain like 15 lbs, always have to wake up in the middle of the night and pee, my knees get shooting pains sometimes at night, light hair by my ears like sideburns, tired, helps with my muscle weakness a little, my eyesight seems blurry sometimes, chest always feels tight. I'm also on Methotrexate, Bactrim, folic acid, and Fosamax. it might be a reaction form all these but i think its mainly from the Prednisone. i cant wait to get down to the lower doses. i look like a different person and even tho all my family and friends know its still embarrassing. i fell like a whole different person. i cant wait to be normal again.

This is my second course of Prednisone after several UC flare-ups. First time I was on 40mg for 2 weeks, then tapered down for two weeks. My first few days on Prednisone were great. I finally had energy, I was in a great mood and finally felt like I was living again. After 4-5 days, the weight/bloating began. My fingers and ankles began to swell, then my face. I no longer felt "alive" anymore, more slovenly. None of my clothes were fitting either. I developed a very noticeable "muffin-top" that made buttoning my pants difficult and wearing and snug t-shirts embarrassing. I returned to my doctor after my two week course (prior to tapering) and found that not only did I gain 12 pounds in two weeks, but my blood pressure had increased dramatically. I was assured that once I quit the Prednisone, my weight should return to what it was, as well as my blood pressure. Sure enough, they did.

I would have to say the very worse part of taking this medicine, for me, was not the two weeks that I was on my 40mg course, nor was it the two week taper, but the two weeks after stopping the medication. My energy level was completely zapped, but I couldn't sleep. I also had the worse headaches and mood swings. I would snap at my family for the smallest of reasons. This medicine introduced a side of myself that I never want to meet again.

Unfortunately, here it is 2 months later and I have been prescribed another course of Prednisone due to another colitis flare-up. I thought I was prepared for what this medicine will do to me since I experienced it once before. However, this time is nothing like the last. Unlike last time, I have yet to feel "on top of the world". My bloat came on quicker this time, as did my mood swings. I am depressed and really hating what I have become. Fortunately, I have enough sense to realize a lot of my depressive thoughts and mood swings are a result of the Prednisone, but it doesn't make it easier. My vision is blurred and for the first time I understand what others are talking about when they speak of foggy brain. I am physically present, but definitely not coherent. I just want this medicine out of my system. I would rather deal with the intense cramping and bloody stools from my colitis, then have to ever go on this medicine again.

was put on toprol 25mgs. one year ago by my heart doctor, for tachycardia which only happened after stress. soon thereafter i developed a numbness in the toes of both feet. i saw my my intrenist who didnt know what it was from. i left the country and was livinf abroad until aug 07. while ther the paresthesia of my toes got worse and started traveling up my foot and half of my calf. saw my internist and was advised to see a neurolgist. he put me thru a series of blood test and an emg. all came up negative. went back to the internist and asked her to review my records from sept 2006. first thing she noticed was that i had been started on toprol. she told me one of the side effects is paresthesia of the feet and or hands, and advised me to cut the dose in half for a few weeks and then in half again in a effort to wean me off of it. its been only 3 days since i began to cut down and already the numbness is starting to decrease. has any one else experienced this? does it go entirely away? please write. hopefull

Hello, I'm a 42 year old, average weight woman, just starting Advair...already I just feel vaguely uncomfortable: light headedness, general malaize, breast-tenderness...I think since my asthma is only mild, I'm going to try some alternatives. The asthma seems to have started with allergies, so I'm going to make an effort first to keep the allergies in check, to hopefully avoid bringing on the asthma symptoms. Has anyone else experienced the breast tenderness? And I've gotten a few itchy hives . Anyone else get those?
Thanks,
Tina

Just a quick update about my husbands law suit with doctor who gave him 6 shots of kenalog for gout in his feet, legs, and knees. Russell ended up rushed into hospital with steriod induced diabetes and was told he would be inusulin dependant for the rest of his life, although his records went missing from hospital shortly after he was admitted. the doctor acting for the solictor came to examine him and has told us he has found letters from the hospital to our doctors and the interesting fact that I think everyone should know, he told us that the manufactors of kenalog suggest a maxium dose of 80 ml he told us Russell was injected with 320ml. We were also told that even though what he went through was very frighting because he did not die, we haven't got a positive case for sueing the doctor. ( but we still are continuing with the law suit)
Russell is not using insulin anymore as the steriods have came out of his body and his pancreas started again, although he is now classed as diabetic type 2 ( diet controlled)
Regards
Tina and Russell ***

Hey, my english is´nt the best, but I hope you understand little!! I have been taking Yasmin for I month because I have pms and skin problems, but I have more acne than ever now I look terrible...... on my neck and jaw big pimples every were on my face... will this be better, would I give it a chance or stop?? I´m from scandinavia and there isn´t so many people taking yasmin there and I haven´t found any forums to talk abot it! Please answer me if you can I would be very happy, thank you! Tina