E mail symptoms and conditions

One of the newest thing my daughter is experiencing is, her joints in her body hurt alot. Mostly in her knees and ankles. Anyone experiencing this?

I'm so glad I found this website - thanks to all of you who have shared. I had a Kenalog injection in May 09 and about a couple of months ago noticed an indentation in the side of my leg. I had it given in my leg instead of buttocks due to other health issues currently going on. It is sore sometimes and hurts sometimes when I bend down or exercise. I also had abnormal periods for several months and didn't realize that it was related to the injection. I had a sinus infection/ear infection and had to get on a plane to go out of the country the next day, otherwise I would have never done this. No one mentioned (or I think knew) anything about the possible muscle/skin side effects. Does anyone know about a class action suit regarding this? I've already made a report with the FDA. I am working with a dr that is doing soft tissue work on it weekly, this does seem to be helping, the indentation decreases quite a bit, but it the indentation increases if I don't have the soft tissue work. I'm hoping I won't have to have plastic surgery to fix this, but looks like I will looking at all the other postings. Does anyone know of a class action law suit regarding this? I tried the person listed in Delaware's e-mail listed on the posting, but it wouldn't go thru.

Hello. I haven't posted anything in a couple of months, but as usual, I'm always searching for more information on natural supplementation that may help your blood pressure. If you're interested, please e-mail me and I will send you the information links. Take care :-)

I had to re-add my original post as it was deleted.. did not realize that personal information (e-mail) should be put in the post. It has now been 3 days since I have had the Mirena taken out. I feel about a 20% increase in my energy.. My hair is no longer falling out in the areas that I would normally be able to gently touch and pull out about 30-40 hairs..and my skin already is starting to calm down even though that was not really that bothersome to me. I must say that my OB is wrong. It was the Mirena. I did not expect my hair to stop falling out so soon, but I am certainly not complaining. I will continue to monitor and advise through posting so hopefully that will give some High expectations to others who were having the same problem.

I have to say to the ones who are noting that they have not had any problems with Mirena that I too did not have any real issues for over a year. I got it in 4/30/08. Maybe 2 months later I noticed the hair and skin being oily.. was no big deal to me.. felt I could deal with that. Then I noticed fatigue and heart palpitations that I forgot to mention as a side effect (every now and then maybe 5 months later). And then around the same time I noticed my feet tingling and my hands on one occasion turning bright red with my veins bulging.. at that point I started to research Mirena.. read some posts.. but didn't think that was my problem. June of this year is when I noticed and nickel sized bald spot on the right side of my head. Because my hair is long and pretty thick I could Hide it and thought I had better get this out of me. I couldn't right away because I have a high deductible on my insurance. Well I just got it out this past Thursday because I found 2 more spots that could be considered 4 because of the pattern of balding.. so Please pay attention to your body. I do agree with my OB that it is probably not the medication.. I think my body was reacting to having the actual device in it and was recognizing it as a foreign object and was trying to fight it off..causing an autoimmune response. As I mentioned.. my hair is no longer falling out.. the only thing that changed was me taking the Mirena out. Please pay attention to your bodies because I don't think the side effects happen all at once. I am just happy that it seems that it has compromised my hormonal balance and hasn't caused any thyroid issue.. but I have a doctors appointment with my PC to get further testing done just to be sure. If any of my symptoms reappear or my hair begins to fall out again.. I will update. !!

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've been on Prednisone for about a month now and have experienced the racing heart. I've been thru so much lately and hope we can help each other here....for the asthma and other reactive friends - try an ALCAT test. This will tell you what foods/meds you have an intolerance to. They send you a kit and you may be surprised what happens to your body when you consume something that your body doesn't like. They have also just given me a script for Methotrexate because my RA numbers are high...I've done my research and so far am refusing to consume that toxic drug. Has anyone tried Minocycline (or other drugs in the cycline family) for joint pain, RA??? I hear it works and at least those side effects aren't deadly.

Ayurvedic Herbal Treatment for Hypertension

Hello. I have been dealing with my hypertension now for approximately 1-1/2 years now and those of you that have read my findings through my previous posts know that I'm always looking for natural supplements to stay off of the lisinopril. I stumbled onto a new herb for bp. You absolutely have to try this. I went to see my doctor yesterday and I was having a really stressed out day dealing with a family crisis and my bp was 150/100. I left with a prescription, but I received my order of this stuff in the afternoon and I took the recommended two tablets twice a day and woke up this morning with my bp 108/69. This product gets shipped from India and takes approximately two weeks to arrive by registered air mail, but very much worth the wait. I have the link to order it and to read more about the herbal treatment. If you are interested, feel free to e-mail me and I will send it to you. Take care and good luck.

I have had asthma since i was 10. I am 44 years old now. I have never in my life been on prednisone this long (since Feb 2009). It is now July 11,2009. I was admitted to the hospital for IV steriods (prednisone) because for the first time in my life the general 10 course with the pills wasn't working. so there i was on 165mg of pred every 6hrs. After eight days in the hospital i was released and was to take 40mg for five days and decrease by 5mg until done. I didn't do to well and had severe exhaustion where i couldn't even walk 2 steps the next day. so I went to my pulmonary dr. who said he noticed a severe anxiety side affect in me from the drug and said i needed to get off it as soon as possible, he had me drop my dose every day by 5mg. TO FAST! I had breathing problems again, started over going slower, got down to 10mg and had to jump to 40mg again! side effects for me are severe anxiety (which i have to take ativan for) and especially massive painful foot cramps. My hands will cramp to while trying to write, but the foot cramps and the feeling of being wired are the worst. I am still trying to wean off....sometimes i wonder if i will ever finally be off this stuff. I just want to cry sometimes. It feels like being pregnant and going thru post partum at the same time

I'm 15 years old and i've been taking prednisone for a few months, and from what i've read i'm on a really high dose. i was diagnosed with rheumatoid arthritis and another autoimmune disorder concerning my muscles at the same time. my doctor told me prednisone was my only choice; it was either that or i would lose the ability to walk. he told me there'd be side effects, but i had no idea it'd turn out like this or i would have fought harder for another course of action. i started out on 30mg twice a day, and since then was weaned down to 20mg twice a day and now i'm down to 30mg once a day. i've been looking up a bunch of information trying to figure out if there's a way to lessen the side effects or any hope at all that they will get better. apparently there isn't much. after reading a bunch of these stories i gotta say i'm not feeling great about this. i totally understand everything everyone is going through. i'm sure you can imagine what it's like being smack in the middle of high school with a huge puffy face, acne so bad on my face, chest, back, neck, and shoulders that wearing a bra could put me in tears, and mood swings so bad i've lost friends over it. everyone knows how brutal high school can be, where appearance and attitude are everything. and i try to tell my doctor about it and he literally looks at me like i'm a whiny teenager and says "you're just going to have to deal with it." and people like my mom and my closest friends don't get it either. nobody understands how beyond frustrating it is. i'll get into the worst moods and not have a reason for it, but i'll stay angry for hours or burst into tears over someone looking at me the wrong way. it'll get to the point where i have to isolate myself from other people because the abrubt mood changes get so bad. as bad as i hate to admit it, the pain from the arthritis is gone now and supposedly my muscles are doing better too. developing arthritis caused me to have to quit cheerleading, something i've loved doing for 6 years, because the pain got to the point where i couldn't get my arms above my head or bend my knees. however, i'd almost rather deal with the horrible joint pain than deal with the side effects of prednisone. if your doctor gives you and alternative method, take it. i've always been confident in the way i look and really outgoing and happy and now i sometimes catch myself thinking about suicide. that's shocking to me because i've got so much going for me, but this medicine makes me miserable. and when i complain about it, anyone i'm talking to just looks at me like i'm being a cry baby. my mom does too, she'll say things like "you just have to do this. i know it's not what you want but to be honest i'm sick of hearing you bitch about it."
i feel a little better knowing other people feel the same way - like nobody gets whats going on with them. the prednisone does give me days of really great euphoria and days when i feel like i could run a marathon, but waking up in the morning to the acne and huge face puts me to tears every day. i have to pee all the time, usually getting up at 2 or 3 am. i don't sleep well anymore and i do sweat all the time. which also sucks being a teenage girl. i'm always hungry, and when i eat i never feel full so i don't know when to stop. my neck and face have put on so much weight that when people see me in the halls or out and about they ask me what happened. mind you these are people i don't talk to, just ones i know from classes or whatever. and it's pretty bad when teenage boys i've never really talked to ask what happened to your face. kind of a blow to the ego, or whatever is left of it at this point.
i'd like to know if, as my dosage gets lowered, the side effects will diminish and when i'm off the prednisone completely if they will disappear altogether. any help there?
or if there is any way to help the acne or puffy face

my doctor just put me on something called methotrexate or something like that to help wean me off the prednisone, and does anyone know what those side effects will do? or if they'll affect the prednisone side effects?
i'm constantly obsessing over gaining weight and what my skin looks like and what i eat and how heavy my face feels and the occasional pressure in my eyes to the point where i just want to be put out of my misery.
and after reading other people's stories i really don't understand why this drug is still given out as freely as it is. but maybe all doctors are like mine, they just don't get it.
best of luck to anyone who's on prednisone, my heart goes out to you; i'm right there with you
sorry this became like a book it wasn't meant to be this long

Ladies,

I hope you don’t mind a male posting on this forum but I do have a reason for doing so. I am a Coroner’s Officer in England. I will not at this time disclose whereexactly I am based as I need to protect the identity of the family. I would however like to use you as a sounding board in the hope that you can help me, help the family and perhaps, just perhaps, I can help you.

Sadly I am dealing with a suicide. The lady in question, who has taken her own life is in her 40’s, married and has children (all over 11 years). The lady has no history what so ever of any form of depression during her life.

The lady has described her life as being perfect with a family that loves her and who she loves in return and as the Investigator I believe she is truthful in that comment. She states she has been extremely happy until last week. She makes comments of - I am just very ill, cannot sleep, feel dizzy, cannot concentrate, sometimes lose my vision, feel sick all the time and sweat at night. She cannot understand, but it makes her feel bad. I am not myself, something has made me ill which means I can’t be my normal positive, active busy self. I can’t bring myself to do anything that I normally love, like gardening, cooking etc. I am losing my memory badly going fuzzy in the head.

Her final comment, which is the one that has prompted me to post on this forum (with the permission of the family) is ‘I just don’t understand this – I’m so sorry . I can’t understand myself or what is wrong with me or what I’m doing so sorry. Just remember I’m not myself somebody else has taken over – I don’t know if it is all the anti-histamine pills that has mixed up my chemical balance along with the Mirena coil or is it just me’.

The mention of the Mirena coil has therefore prompted me to investigate it. I am not, by any means suggesting that this is responsible but it would be wrong of me to discount it after having read the posts on this forum and other places on the Internet.

The lady in question had the coil inserted in 2004/5 and it would appear that there were no problems or side effects reported.

I am therefore looking for some help from you. Some comments on what I have posted etc. Some advice on where to obtain expert advice (although I am trying some avenues of my own).

I may also ask, depending on what help you can give me if you would be willing to identify yourself to me.

Thank you

P.

I have been on prednisone for 11+ years due to having had a heart transplant. The prednisone keeps my heart from rejecting.
I have not taken it for 2 days and I am in the process of passive suicide.
I am driving out west into the desserts to sit and die. I can no longer
be around people for I am afraid I may kill someone or at least significantly hurt them. I have been homicidal and suicidal for 11 years due to this med. I would enjoy killing everyone and everything. I hate myself and I want to die.
Prednisone made me become "Evil"; Hell incarnated. I don't want to live
in a mental institution and my doctor will only give me Seroquel thinking this will help me. I tell him it doesn't help me but he thinks it does. Stupid fucking doctor. My transplant docotrs won't even listen to me when I talk about "mental" issues. Everything pisses me off. It is raining outside and this makes me so mad and stressed.
I have been in this psychotically angry and agitated state of mind for 11 years. I have punched myself many times in the head and banged my
head against walls trying to get homicidal and suicidal thoughts out of my mind to no avail.
I would like to try ECT (electro-convulsive-therapy) but I won't even
mention this to my doctor because he will literally laugh at me and make me so god dam mad that I would enjoy killing him right then and there. I'm sick and tired of living in hell everyday.
Do not take prednisone no matter what, unless your life depends on it. And then what type of life will you have? Maybe a life full of hate, rage, anger, homicidal and suicidal thougts even when you dream.
Fuck life!
Arthur X 1968-2009

Im 23 years old. One of the youngest people that is on coumadin I got sick when I was 22. I developed blood clots on my liver and stomach. Due to blood deficiency. I was told by the doctor it was inherited by one of my parents. My side affects are very fatigue, tired for no reason, skin blotches, slow memory, I get tired after 10 minutes of running like Im ready to collapse. Im always dizzy. =( I feel very fragile. I do get depressed sometimes because I feel like im very young at my age for this to happen. I found out I have to be on coumadin for the rest of my life. But we all move on....

E-mail me ******

Hopefully someone can share there idea's or another source of help.

Hi everyone, I have just read all thirty pages of posts to try to find some answers to my crazy reaction to prednisone. My thoughts are with you all since I have had an usually severe reaction to prednisone. I was on prednisone for 1 week in October 2008 at 60 mg/day for a sinus surgery. I am still having the following side effects at full force:

Axiety to the point I can't socialize
mood swings
hot/sweating even in freezing weather
whole body shakes
severe migraines
tooth sensitivity
muscle pains
extreme thirst (I drink almost 2 gallons/day)
hungry all the time
moon face
water retention around waist
acne
hair loss
rapid heart rate
dizziness
nightmares
night sweats
high blood pressure
high hear rate

I'm not exaggerating, my parent's can contend to that. I do have a history of having sever reactions to medication and I've had all the gland and blood tests which all check out. I never had a single one of these before the prednisone - I was a healthy 22 year old.

I was wondering if any could tell me when this hell will end - my job and well-being depends on it!

*********************READ THIS TO FIND HELP*************************
********************************************************************************
My daughter suffered severe side effects from the Gardasil vaccine - pneumonia, dehydration, etc. etc. The lots with "X" and "U" are causing the most problems. You need to detox your body from the aluminum that was in the vaccine. Please take special precautions if you had the above lot numbers (check with your doctor who administered).
Please read my posting on How to Detox from Gardasil on questions tab. This will help you. File a VAERS report immediately and call your doctor to let them know you are POSITIVE your illness is from the vaccine.
Several people are working on getting this off the market - but please write your congressman or senator to ask that they help. This is the only way to stop this! Also ... tell EVERYONE you know that this vaccine and others with aluminum are NOT safe!

I am 24 and used the NuvaRing for almost 3 years. As I finished up college at 21 and directly afterwards I was becoming more and more depressed, which I first attributed to the transition. It was while I was still in college that I also noticed a change in my ability to concentrate and remember. Focus and decision-making were abnormally difficult. My moodiness and depression increased over the next two years, my sensitivity to other's comments became more acute and I constantly felt at the edge of tears. I had little to no enthusiasm for even my favorite activities, no energy for sports/physical exercise, and no interest in sex with my partner. I required more sleep, always feeling tired when I woke up. I also began to have headaches, which had never been a trouble before.
I have been off the NuvaRing for about 3 weeks. Like some have posted earlier, I feel like a dark cloud has lifted and I can enjoy life again. Notable changes over the last couple of weeks have included:

1. Waking up naturally in the morning, almost 2 hrs earlier than before
2. Dramatic increase in ability to focus and remember (effectively study)
3. Happy mood and few to no self-deprecating thoughts
4. Increased energy
5. Enjoyment of flavors
6. General clarity of thought
7. Return of interest/enthusiasm, competitive spirit
8. Interest in sex
9. Decrease in headaches

I am absolutely thrilled to have identified the NuvaRing as the source of these issues and having eliminated it from my routine. I feel like I have my life back.

DO NOT TAKE DOXYCYCLINE IF YOU HAVE ANY HISTORY OF DEPRESSION!!!

I do and doxy has sent me over the edge for about a month AFTER i stopped taking it.

I was given doxy by my doctor for a sinus infection for a week and stopped taking it just under a month ago. This past month has been absolute hell for me.

The day I stopped taking it I went from feeling fine into a 5 hour crying fit with suicidal thoughts in less than 30 minutes. During the fit I became convinced that this was how my life always is, that I was depressed, that I had always been depressed and that I needed anti depressant as I spend all my time crying. That was on 2nd Feb.

The next day I was shaky and felt very up and downy but went back to feeling normal pretty quickly and after I did some internet research on Doxycycline (the only change in my diet/lifestyle) assumed it was that. I read some pretty bad stuff on the internet about other people’s experiences which were very similar to the one I had had and I thought that must be it.

So I decided to drink lots of water and have been taking Milk Thistle to cleanse my liver.

Then this Saturday past I had exactly the same thing. I had another one of these 5 hour crying fits and more suicidal thoughts and I became convinced I was bipolar. This time was much worse in a lot of ways.

I felt it again felt like a panic attack and to me the change in my physiology was really noticeable. The noticeable dip in my mood – very sudden from feeling fine to feeling a little bit irritable and then withdrawn with some anxiety – and wanting to be reassured but also being a little aggressive in communication almost like trying to find a fight, then a change in breathing and heart rate and then plunge into dark thoughts and sobbing.

When I went to see the doctor on Monday my mood was still swinging up and down and I just felt crazy so I mentioend to him the doxy and he dismissed this without even asking a question about when or how much I'd taken.

I ask to be referred to a psychiatrist as I do get that I may have underlying issues and these mood swings were so bad and so strong and so by the time Wednesday came with my in and out moods I had convinced myself it was probably to do with my childhood and the difficult heart stuff and repressing how I really feel

Whilst I do have my fair share of childhood stuff and issues of the heart I think I’ve become so self aware and so careful with myself and I think I talk to my inner child so much and check that I am okay with things and I deal with things really well. so this has all come as a bit of nasty shock as I thought I was okay with everything. In fact I know I’m okay with everything as I write this.

But during these mood swings I am definitely not okay. I do not feel like myself. I become convinced that I have been lying to myself about being okay, that I have never been okay that I am mentally ill and that is why I am having mood swings and I start really analyzing everything and linking everything back to the past and trying to make links with things that are happening today and things that happened in the past. I haven’t had any change in my heart situation that this could be a reaction to, its remained the same for a number of months and I don’t have a problem with it but when I have this mood swing I blame that situation and my childhood together. I start wanting to blame people. I start thinking I have two personalities and I just start trying to find reasons and I have no idea what I feel, who I am or what I want, if I’m telling the truth of if I’ve ever told the truth. I start doubting everything and everyone. My head hurts, I get in a state of confusion and I become a little mean to people. I start trying to blame events and situations, anything I can find. It’s an absolute nightmare. Then I get confused about what I have and haven’t said and agitated that I need to say more to make myself understood. I might be stable for hours or even a day but it happens very suddenly and it’s a really physical sensation, first the dip in mood, the irritability, the breathing will change, I will feel anxious and can really feel my heart beating, like when you are really scared about something – that fight or flight feelings. I then get a really strong sense of insecurity and nervousness and will become really awkward at communication and almost aggressive and rude in my communications and then rueful.

The crazy thing is my mood is just absolutely all over the place in a way it has never ever been before, even in my days of deepest darkest moments when everything in life sucked and people were horrid to me. I don’t understand why I would, after all my years of learning how to deal with this and cope with this be even worse when my situation is so much better. It just doesn’t feel like its actually real. I don’t feel like anything I’ve said when I’ve been in these moods is actually a true reflection of how I feel when I am out of the swing.

Then I come back to feeling more like a version of myself but not quite and then I swing again very quickly and go from very hyper and laughing to almost the polar opposite in a very short space of time.

This is the first time in a week that I’ve felt like I am completely normal again. Right now I feel very calm and grounded and rational like I have been feeling for a very long time and I feel very clear in my head that I am completely fine and this is a reaction to some chemicals in my body affecting my mood rather than a psychological issue.

I am fully prepared for another full scale attack of mood swings and totally losing the plot again though.

I am lucky in that I have a good friend who called a doctor friend of his in the US and the first thing the doctor friend said when asked about Doxycline was 'don't tell me, you know someone who's had anxiety attacks and suicidal reactions'. According to this doctor this is VERY common and very well documented. There should be no lasting effects or permanent damage and now the doxy is out of my system I should not be experiencing these moods swings.

HOWEVER - he thins that because I have a history of depression due to my childhood issues the doxy has basically destabilised me and driven me to the edge again.

I did some really lengthy research because I really feel like this is a brain chemistry issue rather than a psychology issue and knowing I've dealt with everything and I just don't get why these issues would re-arise. I'm going to go get some therapy no matter what but I just wanted to know the brain chemistry.

Obviously if my GP doesnt even recognise that doxy can have this affect there is going to be no interest in helping me figure this out so I will figure it out myself.

From what I can understand Doxy decreases some amino acids in the brain which is important as simply put, amino acids get converted into neurotransmitters which play a critical role in your brain. Neurotransmitters are the chemicals which help your brain cells 'talk' to each other. Low levels of certain neurotransmitters have been associated with depression and anxiety.

I feel like I am 'back' from the Doxy but to be honest, I have no idea what it has done to my brain and I doubt there has been that much research into it...if so why on earth would they prescribe a drug that does this to people?
Particularly people who have a history of depression.

I am going to try taking amino acids to see if that helps - it can't hurt.

If anyone else is going through the same thing please get in touch and let me know!
This site totally helped me!! Thank you everyone who has posted on it. It really makes a huge difference to know that there are other people out there going through the same thing. I have felt like I am absolutely crazy! Thank you so much :-)

IF ANY OF YOU ARE IN THE RALEIGH AREA AND TOOK THE HPV VACCINATION, E-MAIL ME PRIVATELY!!! The media is picking up this story ...

URGENT - If anyone is from North Carolina - especially the Raleigh area, please e-mail me privately. We are working with a news station to cover these girls. Thanks so much!!!

Hi My name is Daniela, and I just checked my spam box and saw an e-mail about Yasmin dangerous side effects, I guess it is organized by lawyers that wants you to sign up for a law suit..anyway, that made me really think about it ,and I googled to read more about the Yaz birth control. I have been taking Yaz for 16 months, I just stopped taking the drug , because I had to go to the doctor again to prescribe me some more, but since I don't have health insurance anymore I have postponed the visit. It has been two weeks since I stopped the Yaz an for the last 4 days I have had chest pains all around the breast area, my chest and back will hurt at the same time, I got scared thinking I can get a heart atack, or else. I am 32 years old, and It is very scary to me at that early age to have problems like these. But by reading your complains I am realizing the pain is from these pills. The first 4 months I have been taking Yaz, then I switch to Ocella (generic of Yaz) because it is much cheaper.And thinking back then, I started taking Yaz Oct 2007,, In Jan 2008 I went to see my doctor for depression, I got very angry, explode about stuff,and being depressed, and now I am putting all the pieces together, and I can really see all the similar thing that other women has t experienced during the time they took that medicine. Wow, I am glad that I stopped Ocella.And I will go to my doctor for a full exam.
My dad was telling me how a doctor told my brother that his liver look very bad, the doctor thought he is an alcoholic, but he is not, he just takes a lot of pills about anything to get rid of pain, cold, or else. And that info also made me think about myself. And how I should try to avoid pills to take care of minor headache or pain.
Thanks to all the women for sharing their experience, it has really helped me put the pieces together and help myself, by thinking, not by taking pills.THANK YOU

It breaks my heart to hear all the pain we've gone through coming off this drug. Not everybody will be the same. It took me two weeks before i could even go to work after quitting. I took Effexor for 8 months and can't imagine being on it for multiple years. It did work for me,actually to well, and i acted like a 18 year old.(wife didn't approve of that) I've been diagnosed Bi-polar and now on meds that actually work well!
I was lucky in that i own the company and could come and go as i please. I followed the withdrawal thread, so i was prepared for the pain. I created a spread sheet for 2 weeks for every feeling i felt while coming off of it. I put it a scale of 0-100 for every feeling. i must admit it was the darkest part of my life, and yes, my beautiful wife had the common sense to lock all my guns and keep the keys. I wish all the best to anyone coming down from this drug. If anybody is interested, you can e-mail me at ****** and i can send the spreadsheet to you in excel or PDF format. This helped me understand the pattern that i've been going through the past years. It also helps the new doc see how i feel. Just put in the subject "send me a pdf" or "send me a xls" and i will send you the file, no questions asked. I wish we could attach files on this thread. Any doctors interested are also welcome to e-mail me.

I have severe allergies and cronic sinusitis... like a lot of people on here I have taken all the allergy drugs they make for the past 9 years... Ive had tons of procedures done and sinus surgery last Feb '08. Nothing helps. Ive taken oral steriods many times but recently my new ENT decided to give me a Kenalog shot in Sept. Nothing was explained to me other than it was a steroid. The nurse put it in my left shoulder. I have had all the symptoms people are describing on here except the indent. I have been progressively getting sicker and feeling worse and worse over the past few months. I feel like I could go to bed and just stay there. Now this past Monday he gave me another Kenalog shot in my left shoulder. I heard something on a tv show that it causes depression so I jumped on this site and feel sick about all the messages I have read about people's terrible side effects. I feel like my doctor who I trusted let me down. I am so worried that my shoulder is going to have a big grey dent like everyone is describing on here. I am just so tired of being ill.

my three year old daughter has been coughing in her sleep for a few months now so her doc prescribed her singulair because he believes she has asthma. now she is grinding her teeth in her sleep as well. i was wondering if anyone else experienced these side effects. she has only been on singulair for 3 days now and it seemed to start that very first night.
e-mail me at ****** if u have any info

It worked for me but as soon as I went off of it I hit a state of complete withdraw and detoxed for 4 days and attempted to commit suicide, it was so bad I don't even remember everything that had happened...so word of advice if you decide to stop taking this get off gradually and take it very slow!