Boston symptoms and conditions

I just completed my last Lupron shot. It really did wonders for the extreme pain. But the other side effects were extreme such as the anxiety, depression, sleepless night and have just been dealing with the high blood pressure. This decision to take this shouldn't be taken lightly, do what works for you. But always research for yourself!

Just got my Mirena removed today. I had great results for over 2 years and never got another period again. Two months ago I started to have really bad lower back pain and cramps below my c-cection scar. My ob/gyn is wonderful from boston. She removed it and said lets see how you feel in a couple of months. Well as soon as I got off the exam table I no longer had back pain and my cramps are gone !!!!!!!!!!!!

I took Imuran for 3 weeks....150mg/day....started week one with only 50mgs/day, week 2 100mg and then in week 3 got up to the 150mg/day.

Then the aches and pains began....fevers on and off ....and then finally high fevers and rigors ultimately ended up in the hospital in Boston for 4 days.
All of the test pointed to Imuran side effects which caused the fevers etc.

I have been diagnosed with CIDP....and my neuro wanted to put me on a tad more aggressive treatment plan in addition to the IVIg treatment which I am on every 3 weeks, 5x/week. Infusions take almost 3 hors a day...40grams of Gammaguard daily for the 5 days.

I have been on Lamictal for about 3 and a half yrs now for Bipolar 1. Overall, I have had a really great experience with the drug. I started with 100mg and then went to 200mg after a year and a half. Now I take 225mg as of a month ago. For about a year and a half I had the acne on my chin and then it went away suddenly (thought it was cutting out dairy from my diet though). I have been extremely fatigued for awhile now. 7hrs of sleep is not good enough for me so I end up taking long naps when I have the opportunity each day- I always want to sleep. I feel stupid and lack focus and motivation. I use to be a social butterfly and now I feel so exhausted when entertaining. I am a personal trainer and am in the business of making others feel better, but I seem to be feeling worse. I have experienced weight gain as well and that is hard for me since I use to be bulimic and have always had poor body image issues. I was on the NuvaRing for 5 months and it made me sooooo depressed so I finally got off that and feel better- don't mix those 2 drugs.
I am going to ask my doctor to take me off of it this week because I am ready to trust God with my mental health. I have a great support system to help me through the tough times and if I want to get pregnant, I have to go off it anyway.

I just saw an ad for a local news special on WBZ - the Boston CBS station that will address the Singulair problems. This Wednesday at 11:00. I just TiVo'd it. About time!!

Hi Everyone,
WBZTV out of Boston interviewed my family this evening about our singulair experience. They seemed very interested in this story as it relates to how families and individuals have been affected by singulair and will be airing it soon....don't know the exact date yet. My son was able to say on camera that it made him feel "crazy" inside when he was taking singulair and that he feels "much better" since he stopped taking it. We told them we feel lucky to have gotten through our experience but there are so many others who have suffered and are currently suffering very badly as a result of the side effects of singulair.
I think the FDA and Merck now need to stand up and start taking some accountability for a drug that is admittedly "over prescribed". Doctors should be divulging the potential side effects of ALL drugs BEFORE prescribing it so the patient can be fully aware. I mean c'mon the warnings are on page 28 of a 33 page patient information pamphlet. Don't you think it should be on page 1? OK, maybe page 2.
They need to black box this drug. People have lost their lives to it and doctor's need to take their fingers out of their ears!

I'm going to be interviewed about my family's horrific experience with Singulair on Monday by a CBS news affiliate out of Boston. I am going to try and blow the lid off this story and will hopefully be posting my interview on youtube. This has gotten so ridiculous with the ALA "study" ....and I never wanted to go there....but it almost to the point of conspiracy. These people are just downright creepy!!!!!!!!!!

Please be sure to read the article and contact or email the following individual: Heather Grzelka
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I have invited her to review the Medications.com site and contact any parent to discuss the negative side effects that their children have suffered. The word needs to get out about the living nightmare that some families have endured all due to the pediatricians that are not aware of the adverse reactions to Singulair and continue to prescribe this drug.

Let me start by giving you some history.

My sister is a 22 year old girl who worked full time and was never seriously ill until this summer.

During the last full week of June my sister started having headaches. She told me that these headaches were like none she had ever had before. Days later she started complaining that her legs and wrists hurt. She said that her legs were so tired and achy she could barely walk up the stairs. At that time I dismissed what she was saying. My sister constantly wears heels and I chalked up the complaint to a pair of shoes that were not yet broken in.

By July 4th, the headaches were so intense that she went to urgent care. The physician she saw in urgent care gave her an antibiotic and sent her on her way. By July 7th, she was having difficulty standing up and walking was almost impossible. My sister started complaining about severe joint pain. Her ankles began to swell and her stomach appeared distended.

On July 8th, my sister went to her primary care physician. I believe he sent her for an x-ray and said that she had a cyst on her sinus cavity which was causing her to have severe headaches. He then gave her another antibiotic and referred her to a rheumatologist never even thinking that these two symptoms may be related.

On July 10th, my sister saw the rheumatoid arthritis doctor her pcp referred her to. He dismissed her complaints saying that she probably has some form of arthritis, but that there are over 800 forms and it would takes months to pin point exactly which one she has. He then gave her a prescription for Celebrex and sent her on her way. She spent the entire week in bed because her joints were so swollen and achy that she could not move. She actually crawled to go to the bathroom.

By the middle of the following week, my sister's stomach began to burn. She contributed it to being a side effect of the Celebrex and stopped taking it on July 21st. We had no idea that the pain was so bad. My sister's last normal meal was on July 22. By the 23 she had no appetite and could not go to the bathroom. On July 24, the stomach pain was so bad that she could not work, or sit, or function. All she did was cry. She went back to her primary care physician who then prescribed her prevacid to help with the so called indigestion. He told her if the pain continues she could call him. On July 25th the pain became unbearable. My sister called her PCP as directed and he told her to go to the ER. Never once did he say he would meet her there! I brought my sister to the ER where they did an x-ray and cat scan of her stomach. They found nothing. At that time my sister had not gone to the bathroom or had anything to eat since the 22nd. The physician in the ER said that she was literally "full of shit" and needed to go home and take a liquid laxative. My sister is only 22 and my parents were away on vacation. We were stupid and didn't know any better and were so happy that they didn't find anything that we accepted his findings and got out of there.

My sister took the liquid laxative prescribed by the ER physician as soon as we got home. We waited anxiously for it to relieve her stomach pain. After many hours the laxative did not work and my sister ended up back in the ER. This time she was screaming in pain. One of the doctors there told her that if she couldn't calm down she needed to leave her ER. My sister did just that. At this point my parents (back from vacation) took my sister home and called Digestive Disease. A doctor there told my mom to give my sister 2 Enemas. He said that should relieve her pain. My mother followed the doctor's orders, but the pain did not stop. Sunday, July 27th my sister was right back in the ER - this time at another hospital. This time my sister was admitted to the hospital for severe stomach pain. After 5 days and numerous tests my sister was discharged. The doctors found nothing in her cat scans, x-rays or ultra sounds. The pain was more manageable (she was on morphine every 2 hours) and they said she was ok to go home.

August 1st my sister had a great day. She was sitting up in bed and seemed to be in good spirits. The following day she couldn't get out of bed. This time it was neck pain. My sister said the pain in the back of her neck was so severe that she could not lift her head up or move it side to side. By August 4th she was admitted to the hospital again. This time we brought her to University Hospital in Syracuse, NY. We were sure to get some answers there...or so we thought. As soon as my sister arrived in the ER they started treating her with antibiotics. They were certain she had an infection. They then told us they would have to do a lumbar puncture to check her spinal fluid for infection. We thought we would finally have an answer to what was wrong with my sister, so we agreed. The spinal fluid came back fine - no infection. At that time they admitted her to the hospital. While at University Hospital my sister was treated by a team of doctors. They tested my sister for lyme disease, west nile, lupus, leukemia etc. They performed a spinal tap, cat scans, x-rays, ultra sounds, blood smears, etc. All of these tests came back negative. The doctors could find nothing abnormal except for an elevated white blood count -22,000 (it was also very high during her last hospitalization), an elevated C reactor and a very high SED rate. After 4 days of numerous tests and pain killers (first morphine, then Dilaudid, then Dilaudid with a fentanol pain patch) they discharged my sister. The head doctor told her that he believed she had viral meningitis and that it would eventually work its way out of her system. By this point my mother and I were skeptical. We did the research and viral meningitis should only last approximately 10 days. Mig had been sick since the last week in June. No one was putting all these symptoms together. On the day of her discharge my sister started getting her stomach pain back. The pain was mostly on the left side of her lower stomach - under her belly button. Again she was told the pain was due to constipation and she should buy some Miralax when she got home.

My sister was home for a mere 2 days before she would be hospitalized again...for the 4th time. Her stomach pain was back and worse then before. My family could not believe this was happening. My sisters spirits were down and the excruciating pain was making her mentally unstable. This time the ER physician recommended a hematologist come in to see my sister. We just wanted answers so we agreed. This hematologist, Dr. R stated that she believed my sister had drug induced lupus. We were shocked as my sister was tested for lupus twice before and both times the test came back negative. Dr. R explained that she believed my sister got drug induced lupus from the Gardasil shot. My entire family was shocked. We had never heard of any severe side effects like this from the Gardasil shot. Dr. R asked my sister for her permission to test her again. My sister agreed and a week later my sister learned that she was positive for drug induced lupus. My entire family was so happy that my sister finally had a diagnosis and could begin treatment. We were told that after a 6 week steroid treatment (Prednisone) my sister would be back to her old self. We were ecstatic!

My sister was home from the hospital and on the steriod treatment for 10 days when things started to go wrong again. The doctors were very concerned with the dosage of Prednisone that my sister was taking (80mg. I'm not sure how many times a day). They cut the dosage down in half over the course of a few days to prevent kidney damage and other side effects. Once the Prednisone was decreased, my sister started getting sick immediately. Her forearms were very weak - she could not put any pressure on them. Her shoulders would tingle and she would get shooting pains down her right arm. One of her doctors believed she was developing fibromyalgia and prescribed her lyrica. Shortly after my sister began taking lyrica she started seeing stars. She had double vision and a migraine that would not go away. My mother called her doctor and told him about this. His answer was for my sister to stop taking the Lyrica. She did immediately.

On August 29th, my sister still had a migraine. This was day 3 without a break. She woke up early Saturday morning and began vomiting every 30 minutes. After a few hours of non stop vomiting my mother called her doctor. His nurse practitioner was on call and she told my mother to take my sister to the ER immediately. My mother went back into my sister's room to tell her they had to go back to the hospital and she found my sister having a seizure. My sister has no history of seizures. My mother called 911 and the ambulance came to bring my sister back to the ER...her 5th hospitalization.

Shortly after arriving at the ER, my sister had another seizure. Immediately after the seizure the ER doctor ordered my sister to have an MRI. My sister had one during her last hospitalization only 2 weeks before. That MRI was normal. This one was not. There are lesions all over my sister's brain. The neurologist told us that he cannot believe she does not have permanent damage. According to him there is no oxygen going to her brain.The neurologist also explained to us that her brain looks as though she has been poisoned. He said that her MRI is very similar to an MRI of a patient who has been poisoned with antifreeze. Later I learned that Gardasil has both aluminum and sodium borate (which is in both rat poison and cockroach killer). However, according to the doctor once your brain looks like my sister's all the poison is out of your body. My sister's team of doctors started debating as to whether this could all still be from the Gardasil shot...my sister's last shot was on 02/22/08. Some believe that the side effects started off as mild, but since they were left untreated for so long they've turned into a serious neurological problem. They told my family the only way to truly know what is going on is to do a brain biopsy.

Yesterday, my sister was transferred to Mass General in Boston. We were hoping for a bigger hospital, better technology, more seasoned doctors. So far my sister has been treated badly. When my mother told the doctors' about the Gardasil shot and the devastating effects it has had on my sister they dismissed it. When my mom asked the doctors to test my sister for heavy metal toxicity they completely ignored her. I fear that she will never get the proper care.

Hi to all,
I want to Thank all those who contacted me in regards to my request for help with the Media.I believe the reports are in now and the stories will be out soon.I am going to ask that if at all possible ,those that have contacted me wanting to come forward with your stories, let me keep your names for further reference if needed.If anyone does not want that, please reply and I will delete the information.I just cant thank all of you enough,you are helping many by coming forward with your stories.There is great power in numbers and every person counts that is willing to not lay down to this injustice done to our families.If you have a voice and use it, it is a tool to make a change.We all forget that years ago information was passed on by word of mouth,this maybe the only way this will get out until this investigation is over.Use every avenue possible and change will come.Thanks Again Kate and Dave M.

I have never experienced the side effects of statins myself. I have never taken any - nor would I if my numbers should be too high.

I have had the opportunity - or rather was forced to - to "educate" myself on the cholesterol issue as i had 3 relatives suffering from side effects.

They were all over 70 and had taken Simvastatin (Zocor) for years.

In 2003, when I had just got an Internet connection, I started to look for information and was surprised to find these sites:

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I also found "Stopped our statins" (google for those words) where there is a lot of information.

Under print articles you will find a very informative article from The Weston Price Foundation about the different statin studies over the years and also about the side effects.

Are you sure that a high cholesterol will cause heart problems - or is it just propaganda from the pharmaceutical and health industry?

After having visited some of these webb sites and read some of the books you might have changed your mind - like I did.

Your cholesterol is very important for your body and essential for your brain among other things.

Why should you live better and longer if you use medications to lower it?

It`s just to read all these patient stories - what quality of life is this?

I would suggest that you also read the messages for the other statins such as Lipitor, Zocor (=Simvastatin) etc.

All statins have similar side effects.

Here are some books that you might find interesting. Some about the cholesterol issue.

The Great Cholesterol Con (Antony Colpo)

The Cholesterol Myths (Uffe Ravnskov)

Lipitor - thief of memory (Duane Graveline

Malignant Medical Myths (Joel F. Kauffman)

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Overdosed America (John Abramson)

The Truth about the Drug Companies (Marcia Angell)

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Bitter Pills (Stephen Fried)
about quinolone antibiotics such as Cipro, Ciprofloxacin, Levaquin etc.

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The Antidepressant Fact Book
Your Drug May Be Your Problem
Toxic Psychiatry
Medicine Madness
(Peter R. Breggin - all books about psychotropic drugs)
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What if medicine disappeared?
(Gerald E. Markle and Francis B. McCrea)

How doctors think
(Jerome Groopman?)

I needed Metoprolol Tartrate for a very high heart rate for graves desease, I was in the 115's+ lowered too 8o beats per min. Which is great!
BUT, having some horrid side effects.
BAD night chills, intolerance to cold. Shake for 3+ hours then sweat. Feels like I was hit by a train after then I get very nauseasous and light headed
Sleep is bad, toss and turn all night and have a greater fear of the dark
ALSO, my bones hurt all the time!! Never did before, had tests done nothing there.
This is the only drug I could find that didn't make my heart flutter and feel all funky. Its a great drug for just that. All the side effects suck..bad

AMA wants drug ads restricted. Go AMA. Make the drug companies spend the $5.4 billion on real research like how to treat cancer.

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I was put on Prednisonsone for Uveitis, inflammation of the eye. He started me on 20mg at 9 pills a day, then each week it was lowered to 6 pills then now i'm on 3 pills and then next week it will be 1 1/2 pill and i'll be off. I got the puffy face, my feet swelled, everytime i hate my stomach bloated and hurt, my face and neck turns red, i stayed hungry although i fought the temptation of eating for not wanting to gain a lot of weight, which I don't think I've gained any. But now I wake up in the middle of the night and severe knee pain, it feels like my knees they are in some kind of device that is crushing my bones they hurt so bad. i caught a bad cough and it's been around now for about 2 weeks and won't go away, i told the nurse about it and she says, i probably just got what everyone else has gotten, just a bad cough, well what's if it's some kind of infection? I look like a chipmunk, my face is so puffy. When i get off these prednisone in another week I WON'T BE going back on them, no matter what the case. I'm in more pain being on them and have more side effects while on them than the problem i was having with uveitis. I think some co workers thank I'm over reacting, but they're not here they don't see all the pain and frustration i'm going through while on this drug. The leg pain just started this weekend and i Know i can't deal with waking up everynight like this in severe pain. Everyone just makes me feel like i'm over reactin and it's nice to know that somebody out there is going through the same thing. Any comments will be great.

I started taking Topamax 2 days ago and I have already noticed side effects..such as the flat soda...numbness in my arms and face at night...BUT the worst part are the morbid thoughts at night ( I take only 25 mg at night) I have the most bizarre dreams and I wake up feeling like I havent slept for days. I am taking it due to severe migraines which result in seizures. I am horrified after reading some of the posts here. I am wondering if anyone started out with any of these side effects and then as their body became accustomed to the medication did they pass?

I am 49 years old and I have been on lisinopril, 10 mg for almost a year and half. This past summer I developed psoriasis of my scalp and then a few months later I had hair breakage on my bangs and I have severe hair loss in the back of my head with bald spots. I had no idea these were side effects. I also have hypertension and nervousness along with the hair loss side effect. To make matters worse, when I was about 6 or 7 years old I had Sclerderma and was treated at the Childrens Hospital in Boston. I am very concerned about all these side effects and it also states this drug treatment may not be suitable for you if you have Sclerderma. I do not have it any more, however, when I did have it when I was young it did leave a small bald spot in the back of my head, however now the bald spot has spread to a much bigger area. Additionally, my hair is very dry and it was always oily. I would like to know if my hair will grow back in the areas where it has left bald spots once I get off the drug. I found all this out today because I just went on line and looked up hair loss and this awful drug popped up.