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Honor roll student symptoms and conditions

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50 Side Effects posted for honor roll student

September 15th
2008
4:36 AM

I am a mother of a beautiful 11 year old girl, who was a healthy 10 year old little girl until she got her second Gardasil shot! She received her shot on 1-28-08, and started having nausea shortly after (within a few days). She didn't mention it. Within a few months she started having abdominal pain. She was hospitalized on 4-20-08 with pancreatitis. She got out of the hospital four days later. She was on Morphine while in the hospital and went home with Vicodine. She still had residual abdominal pain for the next few weeks, but the doctor said it was normal. She went to school 2 weeks later and started having severe abdominal pain again. We went to the doctor's office where they found out that her enzymes were elevated again. We then were referred to a gastroenterologist. She has had countless blood test..... negative. She has had an endoscopy, a colonoscopy, many CT scans, fecal tests, and now she will be going in for another endoscopy, but this time she has to take the capsule cam. She was so normal before the shots she was boring, but now she has to miss school on a regular basis ( before she was an honor roll student) and has to miss out on some of the most fun school activities. All the doctors act like she is making it up and they think I'm just some crazy mom that wants to drug my kid. They keep wanting to label her with IBS, but she has no signs of IBS other then the abdominal pain. She now has been on several meds. with no help. She now has joint pain headaches, blurred vision, and she says that she feels weird, with no other way to describe it. I feel like everyone wants to turn the other way rather then to accept that this drug is hurting these girls and focus on treating them.

I know this is tough, tough on the girls and young women that are effected, tough on the parents, and tough on everyone who loves them. Please, just remember that you are not alone! I will fight till I die to try and find out what is wrong with these girls. Just remember that you have options, if you do not want to get your child vaccinated, you can visit ****** and there you can find out what legal rights you have to not vaccinate your children if you don't want to. They have the forms that you need and you can download them there.

I am so sorry for all of you that have been effected by this drug! You will all be in my thoughts and prayers, as always. Just please, spread the word, the more we talk, the more that don't have to be hurt like this. Thank you all so much for sharing your stories! They help more then you know!!!!!!

-- By hougasfam5 | Reply | (1) replies | Private Message me

September 3th
2008
4:21 PM

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.

-- By marissar | Reply | (8) replies | Private Message me

April 2th
2008
6:57 PM

I have a 15 yr old son, that has been on Singulair for 4 years. He used to complain to me about not being able to sleep through the night, he couldn't concentrate at school. He was an honor roll student. Then he became short tempered. He also isolated himself, and no motivation. He would not want to do anything. He was depressed. Does not want to shower or anything. He has absolutely no self worth. He would talk about having these problems and I would just say to him that maybe it was just the changes going on. New school, changes to his body, it's just those times where changes and expectations are harder. Some handle it better than others. Than everything just continued to go down hill. My son is very intelligent, so when mom did not listen, he decided to self medicate. Went online to try find out what was going on. Tried to find what would help him. He learned quite alot about pharmacology(spelling???) at any rate he then started experimenting with other drugs. Prescriptions drugs. He just wanted desperately to be happy. I found out about this. He was getting into trouble at school, grades fell. So we then sought counceling and then a psychiatrist. They put him on all kinds of meds. Prozac, Ridilin anti pshychotic drugs. You name it my son has probably done it. Now my son is an addict. I now hear all these things about Singulair don't know what to think.??????? I have had him a drug treatment program of which he was kicked out for overdosing. Then, the hospital of which just put him on more drugs. I don't know what to do. He has asthma, when he does not take his Singulair the asthma really kicks in. I know this we are going to look for something else to treat his asthma. I need input. My thoughts are simple. I believe that it is possible that the problems my have started with Singulair but then my son took a step further. I think to try to survive. But in the mean time he is now an addict and I'm scared of whatever permanent damage that may have occured over the years. Are there any other parents out there, that think their teenager might be going through the same problems? If so PLEASE reply to this message.

-- By desperatemom1 | Reply | (4) replies | Private Message me

March 29th
2008
7:58 AM

Be very wary of this drug! My son was on it for a year and a half ...the last six months were a veritable nightmare for him. Severe anxiety issues (had to be hospitalized at one point ) and depression. Doctors kept saying it was not the medication but when I googled the drug side effects and stumbled on a blog about singulair problems , I told my son and off the medication he went. Within a month he was back to his normal self .
Thank goodness he was old enough to tell me how he was feeling ( 17 years old at the time) but what about very young children on this drug...how can they voice their problems when they don't have the vocabulary or knowledge of what is "normal"?

-- By shadowkins | Reply | (1) replies | Private Message me

May 27th
2007
11:13 PM

I took this pill for 2 years. Soon after starting I became severely depressed. I was hospitalized for depression twice while on this drug, and began self mutilating. My mom heard from a coworker that Yasmin causes depression, and she took me off the drug. Within two weeks I felt better. And I'm trying to get my life back on track. I am happier now than I can ever remember being. Now, even at my lowest points, I am still happier than I was for the two years I was taking Yasmin. I went from being an honor roll student, and now I am barely graduating. Please, if you are experiencing depression after taking this pill, take yourself off of it. Nothing is worth feeling like that.

-- By sarahlynne | Reply | (1) replies | Private Message me


 

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