Tumor symptoms and conditions

Hi there... I came off of Yasmin just 2 weeks ago and thought I should share with you my story since yours is a skin issue. I took Yasmin for 3 years. This past year I would wake up some bumps on my lip.. then on my hands.. then (this is over a period of months) I would wake up and have a slightly swollen lip... this was over the last year or so. I would also get a feeling in my throat, like something was in it and swallowing felt funny.
WELL, 2 weeks ago, I took my bc like I always do, right before I go to bed and my lip starts to tingle and itch.. and in the morning my face was swollen 3x the normal size on on side, mostly at the lips... I couldn't really talk.. it was like those awful photos on google. It was angioedema and can kill you by swelling of the throat. I had also for about a year- an ear issue.. it would sound like I was talking under water and felt like swimmer's ear- related to the swelling I found out later. Turns out I'm allergic. I developed this allergy over the period of time I was exposed.

I just want to say to anyone out there that has FACIAL/LIP SWELLING, or swelling of the hands... GO TO THE ER. It can kill you. I got lucky.. my swelling started slow and after about a year if was full blown. It is not something to mess around with!I was prescribed an epi pen. I developed an allergy to a preservative in it and I'm not an allergen sensitive person. That was just the parms/doctor guess I might add.

The first year I took Yasmin I had numb and tingling toes. and the whole tie I've had on and off leg pain.. no sex drive, that's the truth..definite bloating issues about 6 lbs weight gain, sometimes more without change in diet. I haven't noticed any hair loss thankfully. Migraines. Lots of nausea in the morning, every morning like morning sickness. Car sick even when driving.. not normal! I used to work on an airplane and I never got motion sickness.

I'm now on day 4 of Mirena IUD and I'm having having severe diarrhea and trouble sleeping.. I really, really don't want to get pregnant. Our next step is a vasectomy for the hubby. I'm 25 and I weigh 140 5'10 if that helps. I wasn't an 'at risk' like the pamphlet said.

Does anyone here ever had any tingling issues? I had total thyroidectomy in Feb. 2009. Felt good the first month or two and have gone down from there! Some days are good, some are bad. Never know from day to day how Im going to feel! I started out for about a month and a 1/2 on 125 levothyroxin.....then my doc lowered it to 100.......as of July 14th, Im now taking .88. The tingling Im getting is all over my body, different places, here and there. Ive had some heart rate issues for a couple of months now too and finally had my regular doc send to me see a heart doctor.
Thought maybe the tingling could be from low calcium.....it was normal, CBC was normal, ECHO was normal.....waiting on the holter test results right now. The heart doc gave me a prescription for Toprol. I told him I wasn't going to take it cuz sometimes my heart feels like its barely beating and Im afraid it will make it worse. Im glad I didn't get it! Ive read of too many side effects.
Palpitations, kinda fast heart beat with pounding.....sometimes it feels likes its barely beating! Most of this occurs when first laying down......every now and then while sitting, etc. I do not exercise.....and should but just don't find the time. I switched jobs around the time I found out I had several nodes on each side of my thyroid. I was getting tired a lot and just thought i worked too much. I went from a physical job to a sit down, 12 hour, graveyard shift. Since the surgery, Ive felt it more. Im tired of feeling like crap all the time......I was already going thru some perimenopause stuff before all of this! Before I ever found out about my thyroid, I did have real light pounding of heart when laying down and tingling every blue moon, but very mild as well.
Now with no thyroid.......and medicines with all the side effects......IM GOING NUTS!!! Right now the moodiness and tingling are whats bothering me the most. Some days Im really tired, others Im ok. My body gets hot off and on, no fever. The past 3 days my calves, feet, and ankles have started to swell........never before! Plus I get some throbs and pains in my legs and arms and under my arms here and there. I probably need a new doc and I change of medicine......but Im afraid.
For one, Ive decided to go back to a physical job........and hopefully it wont screw with my heart rate even more. Ive read up on tingling........Im guessing maybe its from all the damn stress since my calcium was normal. Does anyone here have any suggestions?????

hi. just thought i might warn you for whatever it is worth. I have been on mirena for about 4 years. it was my answer from god sincerely because i had terrible periods. my period got so light it basically disappeared. yes!
then about 2 years ago, i started with terrible tension headaches, slowly they began to rule my life-- so that the only relief i got was going to sleep at night. only to awake with the same bandanna wrapped around my head so tight i could barely take it. but with 3 kids grown, a business to run, i figured it was stress. then i started with dizzy spells, almost falling over in the bathroom. A CT scan revealed that i had chronic sinusitis- but something i have lived with all my life. no tumor thank god. so what next-- guess what-- yes over the years the hormone from this drug has overloaded in my system. so make your own decision. was good while it lasted but it will take a while now for it to get out of my system. starting to subside. thanks.

Got married about a couple years ago and went on Yasmin. First BC and as I've never had any BC did not know what to expect. I felt fine but now reading all these makes me realize that the weight gain, NO SEX DRIVE, NO VAGINAL MUCUS (have to use tons of lubrication), re-occurring thrush could be attributed to Yasmin.
I stopped Yasmin last year December as now ready for a baby, its been six months and still haven't conceived, still dry and use lubrication....and also have milky discharge from breast but not pregnant. Had an MRI scan and showed pituitary anenoma (not sure of the spelling) basically a small tumor of the pituitary glad that secretes too much prolactin in system caused by imbalance of hormones.
I'm only praying to God for healing and hoping that my body would go back to normal rather than start other medical treatment.
My advise.............. come off Yasmin, DO NOT TAKE ANY BC

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?

My Mom was prescribed Levofloxacin ( AKA Levaquin) by her retarded doc for a mild cold and a sore throat.
After taking 2 tablets of 500mg each my mom is down is severe pain all over her body! she has joint pains, neck pain, arms, palms shes got severe pain all over her body!
She also has severe itching on the palms and her arms as well..
Headaches,
Things aren't looking good.

She in real pain! She tells me she just wants the pain to stop and that she was better off with the cold and sore throat.

She has stopped taking Levaquin.

Anyone got anyway to help her? something?? She is asleep now but tmr Im going to ask her to drink some kefir..

Thanks

I am 34 years old. Back in 1985 I had most of my thyroid removed, due to a tumor attached to it. Since I was 10 until my late 20s, I was on Synthroid. By age 19 I had 3 knee surgeries to remove arthritis. I have suffered most of my life with joint pains, dry skin, weight that is like a roller coaster, and being tired most of the time. In my 20s I was put on Levoxyl. I has been on Levoxyl for several years now. Since being on Levoxyl I have been fighting anxiety, racing heart, joint pain in fingers and ankles, sudden dizziness to the point where i have to sit or pass-out. I feel like I'm 80 and not 34. After reading this site I am printing all this out and taking it to my doctor. No telling how much damage has been done after all these years.

I had Mirena inserted Nov. 2007 after the birth of my baby girl. I went from an extremely high sex drive to NO DRIVE at all. I had unexpected brain surgery 3 weeks after my daughter was born to remove a tumor, so I thought that I wasn't ready mentally or it was all the medications I was taking, I was never informed on any of these side effects (shame on me for not checking into it more- trust me I paid for my mistake by having my sex drive abolished). Two days ago, I noticed something poking me, upon investigation - The Mirena had completely come out. I discovered this about an hour after having sex!! My husband and I are not ready for a third child so I pray that I am not pregnant. I have yet to read another story where one has actually fallen out, so it must not happen that much. I hope I get my sex drive back and make my husband feel wanted again after a year as I will not be replacing it with another Mirena, I would have never had this inserted had I known there were sexual side effects because a high sex drive or any at all is now very important to me. I am now researching Paraguard, and aside from a regular to heavy period it sounds good to me because it is hormone-free. Aside from no sex drive and it falling out, I did not have any other issues like others have had with hair loss, cramping, etc. We did have the issue of my husband feeling it during sex every once in a while because there is a limit to how short they can cut it. In the beginning I had light spotting every 3 or 4 weeks for several months and then at about 1 year, no period at all. I have had more depression than usual, but we have had a lot going on in the last year so I can not blame the Mirena for that. Aside from the sex drive issues it worked very well for me and had it not fallen out I would never have been reading all these forums and educating myself.

Wow! Let me tell you my story: I was first diagnosed with HBP (170/140) during a high school sports physical in the beginning of 8th grade (I was about 14 years old). I was in top shape and a very healthy eater. I had probably (from what I remember) every test done to see what was the cause of this hypertension - and the only thing found was that my kidney's produce too much renin (the hormone that increases BP). I was then put on Lisinopril 10mg. Everything continued good for about 6 years - I also stayed in shape and ate healthy. However, throughout those 6 years, I did notice my curly hair turing straight and my incredibly (can't do nothing with) thick hair started to thin and become stylable. Now...I do know this is my fault, but in the past 2 years my healthy eating habits have slipped, I've gained weight and started smoking - plus have a sit down, don't move kinda job. However, about 1 year ago, I had a slight spike in my pressure and my doctor added a diuretic (HCTZ 12.5mg) to my lisinopril. Ok, that brought the pressure down and all seemed well. Then..... in December 2008, not long ago, I started not feeling well. Thinking I was sick, I went to the doctor's to find my blood pressure to be 190/140. Immediately, my does was increased to 30-12.5mg. That brought a quick drop in my BP down to 110/66 - I was so darn dizzy I could barely function. I was also but on short-term disability because all this caused me to be off work for so long. Unfortunately, when my dose was adjusted to 20-12.5mg and the dizziness stopped I went back to work. Now, I can't go back on S.T.D. for many, many weeks. And....... The past month has been complete HELL!! My hands (mainly fingers) and toes are almost always cold, I've been dieting for over a month and am struggling to lose weight, my hands and feet go numb more often than usual - I never used to find myself waking up in the middle of the night because of pins/needles feeling, my hair is thinner than ever and stick straight - I'm afraid I'm not gonna have any left, I have UNBEARABLE headaches (sometimes all I want to do is sleep and sometimes, like tonight -it's 4:12am- I can't sleep), I have acne like a teenager - mind you, I never had more than 1 to 2 pimples at a time growing up, and that was rare (I was lucky)... Thank god for FMLA, or I would of lost my job since I've spent so much time home since I thought all was good and went back to work. Only wish I could make a dollar again. Now to top it off...I was referred to a nephrologist (kidney specialist) who after seeing me only once for about 30min and reviewing bloodwork from the end of January (I had a high calcium level as well as some others that deal with the kidneys) wants to take away the diuretic (HCTZ) part of my medication (hopefully to reduce the calcium level) BUT DOUBLE MY MG OF LISINOPRIL. HE WANTS ME TO TAKE 20MG TWO TIMES A DAY. I was starting to think all these new symptoms that came on so quick were a result from the increase of lisinopril - now I think I'm sure. I'm not changing my medications until I can talk this over with my PCP - I'm going to ask we try a medication change. Does anyone have any suggestions? Or any suggestions why a 20-year-old has blood pressure as high as 190/140 with no family history of HBP or really any health problems? Any suggestions why the kidneys are producing too much renin? Any meds that drop the pressure and we don't get headaches - I can live with cold limbs and numbness - it's the headaches that are rendering this 24-year-old helpless :(

I am 34 years old. I am a pharmacy tech. I have asthma and allergies. I have taken singulair pretty much every day since it came out on the market. I've had asthma since i was about 10 years old. I took theophylline as a kid. Steriods on and off especially during times when my allergies are bad. I still use Advair during the fall and spring. Every drug has a side effect. However breathing is pretty good damn thing. Do I have days when I feel low? Yeah. Do I sometimes have nightmares? Yup. Are "natural" products the answer. Not always. The fish oil that some of the posters are touting can also cause GI problems. Some of the natural products contain herbs and other plant derivatives that can be harmful for a child that suffers from allergies. Not proactively treating asthma can be deadly. Some of the parents are suggesting steriods as the answer - those can cause weight gain, growth suppression and can lead to a worsening of asthma.

Singulair has never made me feel like I've wanted to kill myself. I was more depressed and angry as kid when my asthma did not allow me to partipate in normal childhood things. I was sad and hated life when I couldn't keep up with friends at recces because I was having trouble breathing. You have to outweigh the costs with the benefits. I am more irritable when I have asthma flareup then I am on a normal day. For me, I choose to breathe. And singulair has been helping me for almost a decade.

I'm not saying the medication isn't causing these symptoms but maybe there is an underlying cause to your child's depression.

Any drug has a side effect. But without medical research and the medications that come with them - people would still be dying of simple diseases and we wouldn't have vaccinations. As a society, as a whole, we are a culture that looks to someone else to fix things and then blames the people who try to fix it. We need to stop being the "hot McDonald's coffee'" society.

I am 41 and have been taking Yaz for about 6 months. My skin is much clearer and that is nice, but on the other hand I have had a continuous headache for two weeks now. Just in case, I took meds for a sinus infection but the headache has stayed... so now I am being treated for migraines. The problem is: the meds for migraines don't work. I am wondering now if it is the Yaz. When I first started taking it I got headaches at the beginning of each new packet, but now it's non-stop. After reading some of these posts, I am worried that coming off it will also have side effects, but it can't be anything (I hope) like the pain and fatigue associated with a long, drawn out headache. I am deeply scared that this headache will turn into a stroke or a tumor or something.

I started taking Aviane when I was 16 for horrible cramps. When I started having crazy mood swings, acne, and the likes I assumed it was all teenage hormonal crap because my doctor assured me that I wouldn't have abnormal reactions due to the low hormone dosage. Just about two years later when I finally decide to get to the bottom of what could be causing these horrible headaches (which have caused me to think I might have a tumor) I typed up my symptoms and find this. Thank you lovely doctors that gave me this crap! You made me think I was going to die! I'm glad to know that I'm not the only person out there who feels like she's being a bitch for no good reason and can't figure out why. I can't believe all of the confusion I could have saved myself if I had asked for something non-generic.

Do yourself a favor and avoid this crap at all costs. It seriously causes more problems than it solves.

Since having a Lupron shot three weeks ago,my ankles and feet are swollen,has anyone else experienced this?

Does anyone have ringing in their ears due to the arimidex? I have just over a year left to take this drug and I CAN'T WAIT to stop. ( I was a stage 0 (.9 cm tumor/0 lymph nodes)....treated with Chemo (adriamycyn, cytoxin and taxotere), then radiation and now arimidex. ) I was almost 41 when this started, I'm 45 now and want my life back. Don't get me wrong, I want to be cured, but sometimes the side effects are disheartening. This sure does sound whinny and I am sorry. I am happy to be cured, but so tired of all the side effects!!!!!!!!! UGH Thanks, dpr

Two years after taking Chantix a tumor was found on my brain. I also have the pain all over every muscle, bone and joint every day. Do not take risks like I did. I trusted the FDA, and Pfizer and now I regret being so trusting.

I am a 49 year old female I took Cymbalta for 3 days and on the 4th morning I woke up with severe blurred vision and roaring in my ears that was April 26,2008. My ears are still ringing. I clenched my teeth so hard in my sleep I traumatized one of my upper molars which resulted in a root canal and crown. I have been to a ENT to have my ears checked, he said I had minimal hearing loss and gave me lipo flavonoid to take for the ringing. I just went to a neurologist today who is requesting an MRI on my brain to rule out a tumor. I don't know if this is a coincidence or not ,I know the clenching caused the damage to my tooth. The neurologist said ringing in the ears is not a side effect of Cymbalta. My life has been a nightmare since I took it.

I was diagnosed with a tumor called a pheochromocytoma after taking this drug- the drug caused this same tumor in animals

I was diagnosed with cancer of the Kidney and subsequently had it removed; this was after I had been taking Byetta. During the course of injecting the Byetta for my Type 2 Diabetes I suffered from severe vomiting, fatigue, dizziness and just over all feeling ill. I would appreciate knowing if anyone else has had this problem (Cancer in particular) after injecting Byetta.

After a year of battling effects from an eye injury, an optho-neurologist finally came to the conclusion that I had orbital inflammatory psuedo tumor. I was told to take 60 mg immediately and then take 2-40mg doses (AM and early afternoon). On Friday, July 18th I took 60 mg at 6:30 p.m. and was so nauseous and barely slept. That next day I took 40mg in the morning and another 40mg around 2:30 p.m.. Although I had been, throughout the year, experiencing pain in my left eye and cheek..what I experienced by 4:00p.m. that next day was more severe than ever. I started having shooting pain and a headache so excruciating that I was in tears. (I had two children naturally).
By 10:30 I had several hours of this pain when the worst happened. The left side of my face drooped and I had difficulty speaking. By the time I got to the hospital I could not move my left arm and left leg. After five days in the hospital and every test imaginable (cat scan, MRI, EKG, etc) they ruled out all stroke, MS and anything else that would show up on these tests. During the hospital stay (although they did not cite prednisone for this event), they started tapering me off. I went from 80 to 50 in one of these days and thought I would DIE. There was no pain reliever/narcotic strong enough to take away the headache. I spent ten days tapering and prayed every day for the end. Sweating, no sleep, crying and did I mention...my headache has still NOT gone away. I have a couple of hours here and there without this pain but for the most part I have been in this hell even after my taper. The clincher is that NO ONE at the hospital or afterwards would admit that this was a side effect but they also could not provide a response. It took three weeks for me to work my way back to walking and using the left side of my body. Has anyone heard of this before? Good luck to all of you, it has meant a lot to read your comments.

Strange happening. I have pancreatitis with having a Whipple procedure done 4 years ago tying off a large tumor on my pancreas. Because of this I am now a type 2 diabetic with high blood pressure. both stemming from the surgery. Recently, within the past year, I was put on lisinpril. Because of financial reason's I stopped taking the Lisinipril but just recently seeing a new doctor I started taking the lisinipril again and after two days have experienced severe pancreatic pain. Finding out by way of my son in law going into emergency and finding that he too has the same conditions and is taking lisinpril. Doctor's told him Lisinipril should not be taken by anyone with severe pancreatitis.

Had been given Flonaise perscription by U.S.Army allergist. Worked ok got bloody nose from it once and a while. used over a period of four years. All of a sudden woke up to the smell of what I thought was acetone aka nail polish remover. This was not the case because we had no nail polish remover in the house. Every thing smelled like acetone, for up to two weeks. I went to see a nurology doctor and had an MRI done worrying about a possible tumor. narrowing things down we concluded it was the Flonaise. I discontinued the drug and still four years later can not smell much of anything. Once in a while I can smell a slight smell for a moment then its gone. I have been using a "Netti Pot and flushing my sinus's out three times a day. I have had no more problems with severe symptoms of rhinitus. Wish I could get my smell back.

I've been diagnosed with anxiety and panic attacks since Nov. 15 2007 ended at the hospital emergency room, after using Xopenex been using Advair and Singulair due to my asthma once my Doctor increased my Advair from 250mg to 500mg twice a day on Sept. 5th 2007 noticed fast palpitations and overwhelming. Knew and complained for quite sometime that I wasn't feeling like myself. Since Nov. 26th 2007 I stopped taking Advair, Albuterol inhalers,Nebulizers due to the fact of my new Anxieties that I never had. Continued taking my Singulair medication thinking that it was safe. Only been on Singulair a little over a year. Still continued to experience Anxiety and Panic attacks. Due to this I've been seeing a therapist since Dec. of 07.Has affected myself, my children who have witnessed my episodes of Anxiety attacks and know thats not me.Also has affected my performance at my job and attendance. Just took two MRI's of the brain just last week thinking there maybe something wrong with my brain.My side affects have been Dizzy spells,feeling faint,blurry vision,extremely tired,muscle spasms,loss of concentration, and not being focused. These are my experiences with Singulair and I believe that the FDA should further investigate these allegations. I know for a fact I've been experiencing this for quite sometime and my Doctors tell me I'm just depressed. Ignoring the fact they prescribed me so many medications that trigger Anxiety depression and God knows what. Thank you Cita

Has anyone here ever heard of anemia being associated with Toprol? Since they increased the dosage of my husband's Toprol, he has developed anemia and they cannot find a cause but every time I ask about the possibility that it could be the meds causing it (he is on coumadin, too), no one will firmly say no - always a "could be" - so just wondering if anyone else has had this experience. Thanks!

I was on Prednisone for 8 days because of a sinus headache that wouldn't go away. I was also put on amoxicillin for a possible sinus headache. I started on 60 mg for 2 days and than 40mg for 2 days , 20 mg for days and last 10mg for 2 days. The first day I took my headache became 10 times worse and I considered going to the ER. The second day I was suffering from muscle fatigue in my legs and my thighs burned. It also triggered my sciatica pain and pelvic pain caused by ovarian cysts and ovarian tumor. I believe it was the bloating that put more pressure on the sciatica and the cysts that caused the pain. It took a couple of weeks for the sciatica pain to subside, never really got rid of the pelvic pain. I am never ever taking Prednisone again, it has way too many side effects. Also, I think it caused a yeast infection.

I was doing just fine taking 50 mg of Topamax but I was still having minor headaches. My doctor said to go to a neurologist because there may be a tumor to worry about. He doubled my morning dosage and added an evening dosage so now I am taking 200 mg. a day. I started the insanity on Friday. By Monday i went grocery shopping and couldn't remember what I was shopping for. Thank God i brought my husband with me...when I could remember that he was with me. And then when I remembered to ask him what we came for I needed to remember where it was. Upon returning home I offered to help my 7 year old grand daughter with her spelling homework. Do you how embarrassing it is to not remember how to spell first grade spelling words? Tuesday was Mardi Gras and we went to the movies so I was saved any further mind questions. Then along comes Wednesday and I returned to work. Well, I tried to get to work. I got lost. Here I was at Walgreen's trying to figure out what I was doing out at 6:00 in the morning. What day was it? The looks on other's faces when you ask them these question is not something funny. So, I get back in my car and aim in the direction I hope is work. Luckily, I remember where I habitually stop for breakfast. My memory comes back again and I make it to work. I am on time and all is well. Now, the day begins.

I haven't had a period since December. Here it is February. And no, I am NOT pregnant. I can't concentrate. I ate 2 chicken nuggets for lunch and am full (now that is a healthy lunch, huh?). I was addicted to Dr. Pepper and now can't even stand the smell of it. I can't walk and chew gum at the same time. I found a note that I wrote sometime yesterday that really scares me because I don't remember writing it. It says, " Headache @ 1:55 no known trigger jut sudden movement to pick up papers from bin over desk. Nausea as well. Need to go to sleep forever." Good feeling to have? Depression is kicking in.

I just called my doctor and he says decrease the medication down to 100 mg. Ummmm...How about I decrease it down to 0 mg and I take a Imitrex or 2 and a hot bath with a nap when I get home and live to see my grandchildren grow old! I think living with a migraine or 50 is far better than what I have been feeling this past week.

If anyone can tell me that it gets better in less than 2 weeks I will stay with it but 1 more week of this and I will be a patient in a mental hospital. I can't even play Nintendo with my grandson...NOW THAT IS DEPRESSING!