Tumors symptoms and conditions

lower back pain, hair loss,joint pain, complicated migraines, vertigo, palpitation, hormonal imbalances (lowered DHEA, increased aldosterone-it affected my adrenal glands and kidneys), epigastric pain, bleeding, extreme fatigue, anxiety,pulmonary failure etc. I had to go through ER, 2 CT scans ( abdominal and brain), 2 MRIs, neurologist, endocrinologist, GI, gyno etc. I threw my Yaz pills in the trash after the first CT scan that revealed multiple tumors in my liver and left adrenal gland ( i took the pills for about 3 and 1/2 years)... the past 6 months have been a hell, but there are no more migraines, anxiety or other neurological symptoms at this point. By the way, one of my best friends who just started on Yaz recently ended up in the ER last week with a blood cloth in her left lung. Please stay away from that drug!

I am 40 and done having kids. I had the Mirena put in in Jan 2008 to help with heavy periods. Within 3 months I started to feel numbness in my left arm. It would come and go over the next couple of months. Then the numbness and burning spread to my left breast. I developed a breast lump in Nov.08 which was determined to be thickening of the breast tissue (through mammogram and ultrasound) The breast continued to be very sensitive and the arm pain became worse. In March Through a pelvic ultrasound 2 "tumors" were discovered on my left ovary. The doctor wanted to remove only the ovary. Once in the operating room he decided to do a complete hysterectomy. The tumor was a benign blood fill cyst witch burst and also endometriosis was bad enough to remove everything including the Mirena!! Its been two months now and the numbness and burning are still there! I am going to a neurologist to see what is going on. I always felt like the Mirena had something to do with all of this. Maybe I have irreversible nerve damage?

I have had the Mirena for 1 year and 3 months. I have gained 15 pounds in the last year my breast are fuller and put stomach looks like I am 6 months pregnant! I have been having the worst pain in my left side that shoots down my leg. I went to my dr and told her that I thought it was put in wrong, because the of the pain. She had me get in ultrasound and it was positioned correctly and there were no tumors.She said that it could be just that I am ovulating, but I still was not happy with that answer because the pain was just on one side. After several months of the pain I asked her to perform another ultrasound to check it out again, the ultrasound again came back that all was well. My hair is thinning sooo bad, my mood swings are scary. I am sooo tired! The weekends I have a date with my bed and my remote. My kids and my husband are suffering because of the mood swings and my laziness. I am going to have this thing taken out! I want my life back. Oh forgot to mention that I have gas that is out of control!!

I am twenty one years old and I started Nuvaring when I was nineteen and at first experience only one side effect, nausea. In the past two years, I have gained about 15 pounds, despite the t fact that I've been eating less and working out more than I ever have. But perhaps the worst side effect for me is migraines. I have had migraines since I was a kid but I would get maybe 4 a year. Since I have been on NR I get about two a week and the longer I've been on it, the more often I get them. I've had a migraine for the past four days. My main concern is that I love having my period regulated. Before I was on BC I worried constantly about when I would start my period. I never wanted to wear white or a bathing suit in case I would start my period randomly, which happened often. Now I am at a loss of what to do. I have to stop the NR because the migraines are making it impossible for me to function at school or work, but what about the periods?
In response to people's questions about IUDS, I have never used one but I do know people who have. At first it can be nerve racking because it has been known to fall out, but if you are using NR, you know it too can fall out. I'm going to try an IUD and look for a more natural way to regulate my periods. I encourage women to stay away from BC that is hormone based. It's very bad for your body, causing not only these side effects, but blood clots, tumors and cysts. There are other ways and I think we all need to look into them.

I've been searching for answers on LONG TERM side effects of Lupron hoping that it could give me answers as to what's going on in my body now!
23 yrs ago my fertility dr. gave me Lupron to inject MYSELF EVERY DAY (experimental back then). I had SEVERE endo since the age of 16 and was fighting that as well as trying to get pregnant thru invetro. I was 26. At 29 I had an emergency hysto. Now at 48plus I have chronic tendonitis where the tendons will shred off of the joints. I have been diagnosed with C spine and T spine disease, osteoarthritis and a mystery that I'm going to have to go to the Mayo to figure out (hopefully). I have tumors that are growing in my lower back...growing around nerves, tendons and bone, They aren't sure why they are there, why they are growing, or even what they are. Surgery removed 2 of them...but pathology shows foreign matter other than tissue/bone. All they DO know is that it is not cancer. One year ago I started losing weight (25 pds) for no reason. I'm now holding my own at 112 and hoping to figure all of this out. I can't help but wonder if Lupron or any other experimental drugs I was on has something to do with this. Is there anyone out there that used this drug so long ago??

I got my Mirena taken out on Monday. Thank God! I feel better already. The dizziness is gone and I feel good overall. I started my first REAL period today after having my baby November 5th. It's pretty heavy flow and I got the cramps, headache, etc. that goes with it. Even though I HATE my period (don't we all?) it feels good to know I am back to normal. We are using condoms now (he HATES them!). I am looking into getting Essure we've decided one is enough for us (I am only 31, but one is REALLY enough). My doctor was kind of rude, and when I asked her about the Essure, she asked me what I would do if I lost the baby I have now. That's a really rude question, I think. Anyways, let mek now your thoughts. All of your posts are wonderful to read! :)

i had my mirena taken out October 08 as i am 40 this year and wanted to have another child.i had suffered with terrible back aches and tiredness with the coil in so was revealed to finally have it taken out thinking all would go back to normal and that it would only take me a short time to conceive as i always had done in the past. now i find that my cycle will only last about 3 weeks and a couple of days. after i have ovulated i find that i feel very sicky really really tired, i feel dizzy and find it hard to focus sometimes my boobs will stay very tender right up until my period has kicked in and i can feel very low for no reason. i never had any of these symptoms before the mirena and i am still trying to fall pregnant. i no my gp will say its my age but i don't believe that i am still very young for my age and take care of myself. this is all since having the mirena.

I will never take this medication again! I read all the side effects on the pharmacy print-out and didn't see any of the same effects I have been experiencing.

I am hypothyroid and I also take medication for depression so I thought perhaps my meds were not intermingling nicely together. It was a relief to see that I wasn't alone.

I began to panic this weekend, knowing that Thanksgiving is this Wednesday, wondering HOW the heck I was going to muster the energy to pull it off. Plus the mere thought of food makes me more nauseous than I already am.

I just called my doctor because I noticed the pills said '1 refill' on them. Thank God he told me I didn't need to refill them. I promptly told him I wouldn't have anyway, and why I wouldn't. He didn't seemed surprised. I just wish he had let me know this could happen.

2 weeks ago I was happy and full of energy...today, I'm at work wondering how the heck I got here...and how am I going to explain to my husband that, once again, I am going to bed as soon as I get home.

Oh yeah....I almost forgot the headaches . The headaches are doozies...the kind that make you grab on to your head and wait for the pain to subside. I seriously began thinking I may have tumors . This medication is awful... and it makes you feel like a hypochondriac because there are no warnings and the effects don't make any sense at the time.

Thanks to all who posted here!!! You saved me from myself. At least I now know this too shall pass. :)

My daughter is 12 and just started taking Prednisone 5 days ago (40mg - she weighs 105lbs) .. I've been watching her salt intake - tonight she looks a little pale to me - is that a side effect? has anyone else experienced that? She has Ulcerative colitis (2 years this month) - started w/asacol, colazol, 6mp (gave her pancreatits) now is on methotrexate since Nov '07 - was put on prednisone because of a recent flare - to me none of these medications have put her into remisson - always goes 3-5 times a day - sometimes blood - sometimes not - don't know if prednisone will help - so afraid of the side effects -
Dr. said if it doesn't - Remicade will be the next option - after that surgery - only thing - my daughter has never complained of pain - except when she was on 6mp -
sorry for babbling - just so scared...

MY sister is not even thirty yet and has has a full hysterectomy (sp) and will no longer be able to have kids. She started with headaches, cramps, ect after she stopped having periods a year into her mirena use. Then they thought she had cyst, the day of her surgery the found the were malignant (sp) tumors....she fully believes it was due to the mirena.....now i am seriously wanting the one i have out. My hands go numb, lack of energy and now that a year is coming up my period is getting unusual. I was recommending this now i am scared for myself, i have no medical so i is just a matter of getting the money to have it removed and get on new bc. I definitely would not recommend this to anyone. We share the same ob and they assure me it is not the mirena.....and that i should not worry....but after reading more......i know it is the right choice.

My 17 yr old daughter received her first Gardasil on April 17,08 with only pain at the injection site on June 16th 08 she received the 2nd within days she started complaining of severe headaches and eye pain so I scheduled a routine eye exam thinking that her glasses may need to be updated. After her exam her optomatrist called me intot he room telling me that she had severe swelling of her optic nerve and scheduled her for an MRI before we could get that done she went to the ER for severe pain in the eye and headaches there they did the MRI and it was normal no tumors or anything that would cause such headaches. On July 3 she called me from work asking to be picked up because the pain was so bad she could not function at all she was weak, dizzy and overall just not feeling good. I took her to the ER again where they performed a spinal tap and tons of bloodwork and admitted her for pain control on July 5th she had a 2nd spinal tap and every day more bloodwork was performed so far ALL tests ran have come back normal. She was in the hospital 5 days. She seen her ophthalmologist a week after being released and we talked to her about the Gardasil and she felt there was enough "coincidence" to have my daughters pediatrician file a adverse reaction form. That has been done and my daughter has learned to live with the pain since nothing seems to help it anymore. Also the last 6 weeks she has had bad insomnia and nose bleeds.

My son suffered from pneumonia at age 6 months till age 2. They had him on Flovent and Singulair from the age of 1. For as long as we can remember, he has been an aggressive, mean, bitter, angry child. The slightest thing would set him off. The doctors had just had him tested for tumors and cancers and other serious head related problems because he was constantly complaining of headaches. All tests came back normal. Then we heard that Singulair can cause ADD amongst many other side effects, including headaches. We took him off of Singulair and after only 2 days off of it he was a completely different little boy. He is happy and loving, calm and patient. He isn't dissolving in a fit of rage at the simplest thing. We can not believe the difference in how he is acting.
We found about 2 years ago a natural supplement that has really helped control his and my asthma and allergies. It is called OPC-3. It is an incredible anti oxidant that helps with so many health problems! If you would like more info, just let me know. It has been a life saver for our family and many others! Here is a website where it can be found.
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It is under the health and nutrition tab on the left side.
Good Luck!!

I started taking Zocor 6 months ago, switched from Crestor because of muscle weakness. About a month and a half ago started to get fuzzy head and could not sleep thru the night. I awoke up to five times a night and could not go back to sleep. I had tingle feeling on my head above the ears. Sometimes I had to get up from whatever I was doing and walk around and it felt like an “anxiety attack” with a feeling of tightness on the back of the neck. My knees are weak and I can feel them whenever I get up from a chair or getting out of the shower. A few times, I felt sharp pain on my right shoulder blade and my head hurts a lot. Cold and hot flashes mostly at night and sometimes in the morning after the shower and during the day together with the “anxiety attack”. Once in a while I would have warm flush feeling on my face. I also have a few pimples like tiny bumps on my head. I could not carry on my normal daily life for the last month and a half. I could not concentrate on anything except constantly feeling the fuzzy head/head heavy/pressure on my head. I also had a MRI on my head and brain to make sure there are no tumors inside and it came back negative. I just found this website a few days ago and I told my doctor that I am taking myself off of the Zocor for a while. I am feeling at least 50% better already after a few days. I am hoping the rest of the side effects would go away eventually. I feel for you all who have been taking this drug for many years.

You people are freaking me out. I just started today with my first dose of prednisone for my first bronchitis diagnosis. I've been sick for 3 months and thought this would be a good med for me to rid the coughing. I'm starting to reconsider taking any more if all I can expect is long term adverse effects. I took this once before years ago for a severe skin allergy. I got the psychosis initially but then adjusted the dose. Then, I would get euphoric and full of energy, like being on a stimulant. I had no idea the round face thing was due to this, I thought I just ate too much while I was home sick for 2 months. I think I'll try the herbal alternative route. If it works, I'll write again and let y'all know. Thanks for all the comments.

I started Metoprolol 6 months ago while in the ER. I was weak with a virus and every time I got up and did anything, my heart would race and would feel weaker. I have white coat syndrome so while I was in the ER my BP went up to 227/110. They gave me 25 mg of Toprol and a prescription for 12.5 mg a day. I have gained 17 lbs in 6 months, have zero energy, tired all the time, insomnia, and am depressed for the first time in my life,ad I know it has to be from the Metoprolol. I tried to quit it and 3 days later my heart was racing so bad and my blood pressure was real high. I want to try to quit it but am afraid to. Any suggestions on how to quit it?

I HAVE BEEN ON THE NUVA RING FOR 2 YEARS AND AFTER ABOUT 6 MONTHS I NOTICED I HAD A BUMP WHERE THE NUVA RING WAS PLACED. I HAVE NOW LEARNED THAT THE NUVA RING MAY CAUSE A CYST. I HAVE WENT TO MY DOCTOR BUT I HAVENT FOUND OUT FOR SURE IF THATS EXACTLY WHAT IT IS. ILL POST LATER TO LET EVERYONE KNOW WHAT TO LOOK FOR. I ALSO HAVE MOOD SWINGS, NO SEX DRIVE, MIGRAINES, AND OTHER SYMPTOMS.

I am 50 years old...nearly bled to death from fibroids and became anemic. I had extremely heavy periods and had to receive a transfusion of 2 units of blood when my blood count went down to 7. My options were 1) Do
nothing...2) Take 6 months of Lupron to hopefully bump me into menopause....3) Fibroid embellization...4) Hysterectomy. I am trying to avoid a hysterectomy....and needed time to get my blood count up before any other procedure. I have had some of the side affects...hot flashes, mood swings, night sweats,.....but I had them before because I was pre-menapausal anyway so there is really no difference. Have not noticed any weight gain and I get my 3rd shot today. Everyone's body is different...for now Lupron has been a life saver for me.

I am taking Lupron as I had horrible endometriosis, two large-grapefruit sized tumors and several smaller implants removed. I lost my right ovary, and part of my left in the process. I am 28, newly married, otherwise healthy, and I want to have children, so I went on Lupron that my surgeon/OB suggested- monthly for six months. I read a lot of side effects and was TERRIFIED to go on it.

My own husband is an M.D. and I made him call different doctors in his hospital to see what they had to say...in a few days he called about 5 different OBs. Thankfully, they said that those that had side effects that were extremely severe was pretty rare. Still, I was scared.

I am now into my second month on Lupron and I have to say that the side effects aren't nearly as severe as I thought they would be. No hot flashes, no hair loss, no crazy depression, no anything else. I DO have fatigue, but it's manageable with coffee and extra sleep. I have some mood swings- mostly I feel more grumpy. The most noticeable and bothersome is the lack of sex drive and vaginal dryness. I also have trouble achieving "the big O."

Still, so far, very manageable. I'm not sure if it'll be worse if time goes on. But I feel like everything on the internet is really negative. I'm not discounting the tales of people who have had a bad time, but I wanted to put out there that it isn't always the worst thing in the world.

I am so glad that I stumbled on this page so I can warn others so they won't have to go through what I am going through. I began using NuvaRing in August 2007 because I couldn't remember to always take my pill at night. I noticed a change in my mood, I was having major mood swings which was affecting my home life and my work life (I teach middle school), I was having headaches that would last for days. Also, I began having nausea and a stabbing pain in my right side just under my ribs. I went back to my family doctor (who by the way suggested the ring because that is what she is on) and she set me up for gall bladder tests. I went through 2 inconclusive tests on my gall bladder and was still having pain and nausea. I was then sent to a gastroenterologist for stomach issues. I have had an upper GI, CT scan and MRI. The tests showed that the root of my problem was a tumor on my liver. I am now awaiting an appointment with a specialist to discuss the removal of the tumor or what I can do for it. The ring was the cause of the tumor. I am 29 years old and have always been active, working out, I have 2 small children whom I play with often, I used to play bass guitar at my church but I had to stop that because I was too tired to go to practice! The tumors are very fragile and can burst to cause internal bleeding which can be fatal! PLEASE, PLEASE, PLEASE DO NOT START THE RING OR TAKE IT OUT TODAY!!!! There is nothing worse than looking at your children and your husband thinking that you could have internal bleeding that could kill you and you would never be able to see them again because you just didn't want to get pregnant! I didn't read the pamphlet that came with it, I just trusted it because that was what my doctor used. This "rare" incident that happens to like one in a million has happened to me! I took it out the 30th of Dec and have had much more energy and felt better about myself. That doesn't change the fact that I have this tumor that I have to deal with now. I was only on it for 4 months!! Be careful

Could very severe stomach distention be caused from synthroid. I have been on synthroid for years. For the past 6 months my stomach is (like i am 4 months pregnant) it never goes down. Have doctored and haven't found any tumors, etc. Could this be a side effect of synthrod? This is the only drug I was on.
Thanks,
Lisa I.

I have suffered from Fibromyalgia for over 12 years so muscle pain, fatigue and memory loss is a way of life. It concerns me that some of the increased pain and fatigue could be related to Zocor. I have been on it approx on year. The new thing I am experiencing is knots, cysts, tumors what ever they are are showing up all over my body. I have one in the muscle of my left shoulder and have experienced extreme pain with limited use. Has anyone else experience this happening to them? Taking Zocor is the only thing that I have done differently in the last year. Going to the Doctor about all of this in 3 days. Thanks Debbie

I started searching for any side effects of Yasmin after a young lady on another website that I frequent asked about it. I started taking yasmin in 2002 after I had sugery to remove tumors from my ovaries. I experienced such terriblr pain during my menstral cycle right before and right after my surgery that my gyno prescribed it for me. It did stop the pain but my body has not seemed right ever since. I contributed it to my body being confused after my surgery, I never would have contributed it to the yasmin. I had absolutely no sexual desire (and it is still at a minimum), I would wake up in a pool of sweat every night, I have had excessive weight gain. Before my surgery, I weighed 115. At my last visit to the gyno I weighed 160, My weight had not been an issue in my adult life and I cannot seem to lose the weight. Since beginning a serious workout routine, I have had terrible pain in my knees and I battle with depression and for a while had constant anxiety attacks. When I tried to tell my doctor that I thought something was wrong, especially about the weight gain, he said that it couldn't possibly be the yasmin. This site has really opened my eyes. Thanks ladies!

i have been on 40 mg lipitor for about 2 years. I am 44 years old and about 9 months ago, my right ear went deaf. No dizziness...no vertigo...it just went. Went to an ear specialist, hearing test showed i have lost hearing in right ear with no bone or ear drum damage. MRI showed no tumors or abcesses. Family doctor then took me off of lipitor about 2 weeks ago. Have detected no change. Any suggestions for trying to get my hearing back in my right ear??

17 year old female. I was diagnosed w/ thyroid cancer when I was 8 and had my entire thyroid and several tumors removed a month after the diagnosis. I've been on Levoxyl for about 7 years. I often experience chest pain, nausea, abdominal pain, and depression. I want to take myself off the medication, because I recently went 3 weeks w/o taking it and the depression went away. Only problem is when I stop taking the medication for more then a month I start to feel really sick, paranoid, and I'm unable to concentrate. I've asked my mom if we could look into an alternative medication, but she believes my doctors when they say that my depression, chest pain, nausea, and abdominal pain are not at all related to my taking Levoxyl.

My dad and sister both take Lisinopril. My sister has the dry cough that many of you taking this drug seem to have. My dad has been taking Lisinopril for a long time. He is very weak and tired most of the time and has had dizzy spells, or the feeling that he is going to faint. I never knew these things might be connected with the Lisinopril, until I read all the side effects on this site. My dad also had watery eyes, then his eyelids began to swell. His eyes got so bad that one eye was completely swollen shut and the other eye was partially closed. He was diagnosed with tumors behind his eyes and ended up having eye surgery on the eye that was completely shut. The tumor quickly grew back and his eye is swollen shut again. Another doctor (not the one who prescribed the Lisinopril) told my dad that it might be the drug causing the problems with his eyes. The doctor who prescribed Lisinopril never told my dad about the side effects, although he had known he was having problems with his eyes. When my dad told him what the other doctor said, he was taken off the Lisinopril, but within a couple of weeks, his blood pressure shot up to over 180 (It had been around 112 while he was taking the drug). Has anyone else experienced swelling or growths in the eyes?