October 5th
2008
9:25 AM
I have corrected my typing error I am not on 400mg it should have read 40mg. Thanks to the reader of my experience who very kindly pointed out my error!!!!
Despite having a brush with the big C last year (I finished chemotherapy in January) I have been very fit and healthy during my 61 years! A few weeks ago I started having palpitations, hence a visit to the doctor revealed high blood pressure and cholesterol reading of 9.9!!! Shock, horror. He informed me that it was genetic and prescribed Simvastatin 40mg and Bendroflumethiazide 2.5 mg daily. Not being satisfied with the enclosed leaflets I have looked up more info. on the net. Should I have done this!!! After reading some of the posting on the site I am feeling a bit apprehensive. Last night I had a terrible night couldn't sleep for the pains in my legs and a bit nausea this morning. But I need to be sensible, I really don't have any choice but to take these drugs just hoping that I won't have to stay on them for the rest of my life and I don't get any of the side effects that some of you have suffered. I also wonder if the chemotherapy could have caused by raised cholesterol? Hope to keep you posted and would welcome any comments!
October 1th
2008
5:43 AM
Despite having a brush with the big C last year (I finished chemotherapy in January) I have been very fit and healthy during my 61 years! A few weeks ago I started having palpitations, hence a visit to the doctor revealed high blood pressure and cholesterol reading of 9.9!!! Shock, horror. He informed me that it was genetic and prescribed Simvastatin 400mg and Bendroflumethiazide 2.5 mg daily.
Not being satisfied with the enclosed leaflets I have looked up more info. on the net. Should I have done this!!! After reading some of the posting on the site I am feeling a bit apprehensive. Last night I had a terrible night couldn't sleep for the pains in my legs and a bit nausea this morning.
But I need to be sensible, I really don't have any choice but to take these drugs just hoping that I won't have to stay on them for the rest of my life and I don't get any of the side effects that some of you have suffered. I also wonder if the chemotherapy could have caused by raised cholesterol?
Hope to keep you posted and would welcome any comments!
December 28th
2007
3:49 PM
I had Mirena put in straight after the birth of my second child as recommended by my maternity hospital to have inserted 6 weeks postnatal and kept it in for seven months. At first I just had minor symptoms like spotting slight cramps and a little bit of vaginal discomfort due to the wires, and the only good thing was that my periods stopped eventually. As the months went on my health started to decline as the side effects crept up on me and I couldn't figure out what was wrong. I just thought it was because I have two small children and I was feeling worn out/burnt-out, it got to the point that I was struggling to do everyday tasks and look after my children. I am only 24 years old and I felt like I was a 50 year old grandmother!
I had the Mirena removed 3 days ago after reading this site and I feel so much better! This company must know that there are more side effects than they have listed, yet they still fail to list the serious and debilitating side effects their product is causing people. They were sending the maternity hospital I went to products with Mirena printed on to push their crappy product. The biggest worry I have about this thing is that I am breastfeeding and I had this stupid thing in for 7 months and some of it was coming through my breastmilk and I have noticed that my 9 month old baby girl had really bad clicking joints that have got better since the Mirena removal as have mine! (although not 100% back to normal yet) This company deserves to have their product removed from the market and someone to sue the pants off of schering. The product is completely unsafe!. If there are any long term side effects to myself or my daughter I WILL SUE THIS STUPID COMPANY AND THE DOCTOR AT THE MATERNITY HOSPITAL WHO PUSHED THIS PIECE OF JUNK TO ME. The warnings are completely inadequate - because I'm sure if all the possible side effects were listed next to no-one would have it put in. I feel that this thing is pushed on mothers so that you can't distinguish the side effects from hormonal changes that could possibly occur after the birth of a child to hide the fact their product is dangerous.
-- By mumof2_melb | Reply | (5) replies | Private Message me
May 21th
2007
7:09 AM
I am currently on Levaquin because Bactrim did not completely relieve me of a UTI infection. I avoid taking pharmaceuticals at all because I suffered chemical poisoning from living near the World Trade Center and, as far as I'm concerned, ALL pharmaceuticals are poison...but necessary in some cases when diet and exercise are not enough to stay healthy. I have some minor side effects and the infection seems to be clearing. Before I started taking it I looked at this website. I just have to say that I can't believe the number of people who are depending on their doctors and pharmacists or leaflets to give them information. It is YOUR health and YOUR responsibility. Personally, I would never put something into my body without finding out myself and researching it. If someone chooses to not take responsibility for their own body and health, then don't blame your doctor for that. It is your choice to put your health in someone else's hands...and the fault is your own. Don't put your health in the hands of someone other than yourself without doing the research.
-- By pamelagauci | Reply | Private Message me
April 9th
2009
12:55 PM
I am in month 4 of a 4 month Lupron shot that my doctor gave to prepare for surgery. I was told I might get hot flashes, loss of libido, increased urinary symptoms for a few weeks. No one said anything and there was absolutely nothing in all the drug leaflets they gave me that would have prepared me for the the horror story that my life was about to become. As if having cancer was not bad enough.Since day 2 I have suffered so many bad side effects that I have lost count. The worst is insomnia and nothing has helped including high doses of Ambien. They suggested Lunesta but my health insurance company balked and even if they had said yes, my co-payment would be unaffordable. This stuff is more expensive than gold. I am exhausted all the time. I have terrible memory problems that are so bad that I can be talking to some I know really well and not remember their name. I am unable to concentrate on anything, my mood swings are unbelievable, I feel mentally disoriented and dissociated all the time, high blood pressure, racing pulse, high blood sugar, hot flashes, raging night sweats, dizziness, bad balance. The side effects that I can handle include nausea, headaches, diarrhea, joint and muscle pain. I am supposed to be on Lupron for 2 years. The only difference I see with my Lupron experience and others here is that my gender is MALE and I have early stage prostate cancer. Being male, my other serious Lupron side effect is complete impotence which is going to go on for a long while due to the radiation. I had radioactive seed implants into my prostate gland done a week ago and I have to follow this with 5 weeks of beam radiation. Lupron seems to be an equal opportunity drug. Lupron has messed me up so badly that for the past 5 weeks I have been off work on disability status with no chance of going back for at least a month and my Dr thinks that may be optimistic. No one seems to know how long it will take to get back to some kind of normal. I just could not function at work and ended up in my doctors office having a complete emotional meltdown. I would caution anyone, male or female, to consider Lupron very carefully before having it.
-- By gnarly | Reply | Private Message me