Mds symptoms and conditions

I am a healthy, active female on a low dose of premarin from a hysterectomy last year, went on a low dose or Lisinopril last June and within a month, was at the ER twice for heart attack symptoms. My EKGs were perfect, thyroid, electrolytes, etc. and we determined, my sis has two MDs that I was over-medicated because the panic attacks started there after and were nightmares! My doc said menopause triggers these even on hormones, I know my body and I was being poisoned with Lisinopril! Been off a month now and this is my first weekend I felt normal w/no more stroke/heart attack signs thank the Lord! Any ideas on what we menopausal women can take for high BP? There is life after this drug but if it high BP runs in your family, some kind therapy is needed for us middle aged gals!

My wife had Mirena for 2 weeks. Severe cramping. Went to her Dr. and he discovered it came loose and had gone into uterus. While in thee, ir perforated uterine lining. Last night she had Hyseeroscopy and lathroscopy to find where it had gone. It was found resting on top of her uterus. Again, if ALL side-effects had been communicated to us, she prob wouldn'tve wound up in the OR last night.

Hi everyone, I had Mirena pleased about 2 years ago following my 2nd child. I have been experiencing mood swings, dizziness, nausea, and breast enlargement. I feel as though I am pregnant (which I know is rare). I've been suffering from sharp chest pain at times and sharp abdominal pains. Cardiology testing came back normal. I have no sex drive and feel as though I cant lose the weight gain from pregnancy #2. After pregnancy #1 I was able to lose all the weight in a matter of 10 months without trying. I know that this IUD has more side effects then what the doctors are informing us. It is crucial that any woman that has this IUD report all side effects to their MDs. This way it is documented for future research.

Someone PLEASE help or offer assistance! I have been on 50mcg Synthroid for about 1.5 yrs now and have gained about 25 pounds!! I am a very, very active triathlete, not just your 30 mins on the treadmill kind of girl. How about running 5-6 miles, riding my bike 40-50 miles, and swimming all about 3 times per week!! How can a human being continue to gain weight at this activity level? I am considering just stop taking it, cold turkey. Has anyone tried any of the supplements for thyroid support, or natural meds? If you've got any suggestions, I am open to just about anything at this point!!

My daughter is 17, had her 3rd Gardasil shot July 2008. She is not one to take naps and is now taking daily nap and going to bed 1 - 2 hours earlier than she ever has before. She came to me a week ago and told me that she just does not feel good and wanted to know why....could she go to the doctor. Of course I scheduled an appt...the dr questioned her of her symptoms and sent her for blood work check for mono, anemia, thyroid. Talked with the dr today and ALL of her blood work came back Great! dr tells me that all of her levels could not be better. So I ask could this be a side effect of the Gardasil vaccine? Of course he tells me that no there should not be any side effects this long after having had her last shot in July of 2008. So I ask what to do next....long pause....well it might be a virus that is trying to surface....I replied with one that has taken 6 weeks to surface? Again long pause...So I ask the dr what else could be done....he simple said he did not know...this is unacceptable to me! I had a very vital young lady living at my house now have a lifeless young lady with dark circles under her eye living at my house....and to think I thought I was being a good mom having her get the vaccine to prevent cancer not knowing that I was going to take the life out of her....I am just sick for the choice I made for my daughter! Please do not subject your beautiful daughters to this vaccine!

It is too soon to tell if YAZ has contributed to my daughter's problems but her doctor just recommend that she stop taking it immediately.

My daughter is 17, in the last two years she has had mono twice. It all started with spasms in her back and neck two years ago, then her neck lymph glands started swelling and she kept getting horrible viral sore throats. Next her blood pressure started dropping radically. 85/50 for no reason, next she started getting terrible stomach pains and then headaches,nausea, watery eyes, irritable bowl syndrome and then the glands in the area of her appendix swelled up so much the emergency room thought she had appendicitis.It was her glands, not her appendix. This was all over a 2 year time frame. None of the symptoms had any rhyme or reason and they all came and went erratically. However, they were making her miserable and me miserable because she was depressed, very moody and unhappy and sick!

The only thing she has ever taken during all this time was YAZ. I asked her doctor if the YAZ could contribute to the swelling of the lymph glands and he did not think so. That was a year ago. Yesterday, I took my daughter to a Rheumatologist and when he heard she was on the YAZ he told her to stop immediately and prescribed a low dosage of muscle relaxer and an anti inflammatory. I have no way to know whether all of these symptoms are going to clear up. I have started my daughter on a wellness plan of eating which includes lots of holistic methods. Hard to get a teen away from comfort foods when they don't feel well but she is resigned to the fact that her immune system is so compromised that if she ever wants to feel well we have to try drastic measures.

She has had almost all the symptoms described as Chronic Fatigue Syndrome and I am told that's what she has now. It is possible that the YAZ had made all of this worse. She sleeps endlessly and only time off of the YAZ will tell, but as a mom I wanted her off this pill a year ago and I am upset that I didn't do more to get her off it. It took her missing 60 days of school consecutively for a doctor to say STOP and see if it helps. My feeling is she couldn't be much worse, well actually that's the direction this seemed to be going. I think that the estrogin has fed many of the problems my daughter has had, but I am not a doctor and it's just my mom opinion.

Only time will tell.

My daughter was 16 when her GYN started her on Yaz. She was 5 ft 3 and 100 lbs. Non smoker. No risks. She went on the pill because she was having heart palpitations and extreme fatigue that correlated with her menstrual cycle. The idea was to level her hormones and see if that would level off the physical problems. Within 6 weeks she suffered from a pulmonary embolism. Because she was young, everybody though it was just pneumonia or inflammation of the lining of the lungs (pleurisy). Then her leg swelled up and turned blue from a clot (DVT). I found it fascinating that everybody at the first hospital, during the helicopter ride and at the second hospital all had EXACTLY the same reaction . . . They all said, "you just started taking the pill, didn't you? Probably one of the new ones like Yaz." Apparently, these new 'third generation' pills are worse than the old ones when it comes to clots. It turns out that my hubby's history of blood clots should have been a clue that my daughter has a common clotting disorder and YAZ triggered it into action. The clotting disorder affects up to 10% of Swedes and that is where my hubby's family comes from. Up to 5% of all Caucasians in the United States have Factor V Leiden as well. I notified the FDA and highly encourage everybody else to do so as well. The doctor are not required to file a report unless a patient dies. My daughter is doing better now. If any reporters are reading this, please contact me. B. A. ***** If you have ANY family history of problems that might be due to clots, avoid the third generation pills.

Lisinopril has ruined my life! I used to feel great. I was diagnosed with high blood pressure, so my doctor put me on this poison. I've been on it for about five years, and each year have had different medical problems. My bp was high, but not terribly high before this poison (150 over 95). After going on the poison it went down to 130 over 80. I don't think it's been worth it! I've had a dry cough from hell, anxiety, insomnia, weakness, itchy skin, hives, pain in my abdomen, kidney stones, tired all the time, and worst of all it has affected my complexion, as my face is now red from it dilating the capillaries in my face. Luckily I found this site, and made a choice to get off this poison. I went from 20mg 2 weeks ago to 10 mg, and have been off it for 3 days. My blood pressure is slightly higher 138 over 88, but I don't care. I feel much better!! The last 2 nights I slept like a baby, and now feel like my old self. Before the last 2 nights I have NOT slept an entire night through for FIVE years. My skin is starting to go back to its normal color, and I don't fell so anxious. This medication is poison, but the MDs will tell you how great it is. This medication is the silent killer! Anyways, I'm going to go enjoy my day. Good luck.

One year after my shot of Lupron I have severe joint and muscle pain and breast tenderness and pain. I am a male who had the Lupron in concert with radiation therapy for Prostate Cancer. My MDs suggest the joint and muscle pain is a result of arthritis, and a mammogram is recommended for the breast swelling and pain. Any males out there with similar symptoms?
PB

I'm an 81yo Caucasian male who has been taking Lisinopril for two years ago. I have suffered through the aches and pains , dry cough lightheadedness , associated with this drug. When I first took 20mg/day, I tracked my BP as frequently as 20 times per day. Some of my symptoms were a result of my BP dropping down to s practice of medicine, MDs do not always have the time to experiment with each patient, so the patient must do some of the logical investigations independently.
Remember, no one knows your body better than you, and your PCP or Cardio MD only sees you for a short period of time. I have tried five statin drugs and cannot tolerate any of them. Alternate, naturally-occurring substances are available.

Only on it for 1 month so far and already having issues. I apparently have the worst case of endometriosis all my doctors have seen, including a cancer specialist that had to do all my surgeries because of the severity. Granted, I am only 31 years old and have had a full hysterectomy. So, after 3 surgeries I am still having severe abdominal pain and bleeding (don't know where that is coming from since I don't have a uterus anymore) so they said try Lupron and I finally gave in. Now I started getting such severe pain in my lower back that I can't stand for longer than 15 minutes and terrible side aches. I started getting headaches (which I already take pills for for years now),and have gotten the hot flashes as well. What are we to do ladies? I am so sick of complaining to the doctors about pain. You feel as if you are a big cry baby. What are my options here and does this ever stop?

I saw an elderly ENT who prescribed Biaxin XL 1000mg/once per day for a severe sinus infection of the ethmoid, maxillay and frontal sinuses. I was not getting any better, in fact I was getting worse. I decided to go for a second opinion and learned that Biaxin is not as wide spectrum of an antibiotic as Augmentin is for sinus infections. The key strains of bacteria are not being obliterated from the Biaxin. MDs who prescribe Biaxin are not staying on top of current literature as Biaxin was commonly prescribed in the 1980s and 1990s.

My incredible side effects to Biaxin XL (including not wiping out the bacteria) include: lingering bad bitter taste, night sweats, insomnia, extreme stomach cramping, constant stomach churning (which kept me up at night), terrible diarrhea, nausea. The only plus side is that was more mentally alert.

If your doctor prescribes Biaxin for sinusitis, leave that doctor immediately and seek help from another practitioner who is more current on medications of choice for treatment.

WOW, I am so happy to find this site. I am a 56 yr old female. I too am on Toprol. I was on 75 mg 2 x's a day for HPB and mitral valve prolapse pain. Then yesterday the Dr. increased my dose to 100 mg 2x's a day .Today my ankles and feet blew up like balloons. I have been having profuse sweating and was cold and clammy for the past year and no Dr could tell me why!! NO sex drive , depression,sleep apnea, severe insomnia, brain fog, short term memory issues, moody, irritable, my husband has threatened to leave me. NO appetite!! Floaters in my eyes started a few months ago, I have so many symptoms that I have read in all your posts. No quality of life for the past year. I have felt like I was losing my mind, gained 35 lbs in past 2 years without changing my eating habits. I gained the weight after I had lost 50 lbs. Been on Toprol about 2 1/2 years ( I think ) Every symptom I have experienced I have read in your posts!! I have type 2 diabetes and am on glucophage, I also take 10 other scripts. I have fibromyalgia and chronic fatigue, RSD in my left arm, muscle pain and joint pain. Pain in my right upper qaudrant. Nausea/ some vomiting, NO ENERGY, Loss of interest in most of life. So now after reading all your posts I have to ask myself, are all my symptoms linked to the Toprol and not syndromes or illnesses? I am calling my doctor in the morning and getting off this med!! They will just have to put me on something else!!!
So how do I post to receive replies?
Joyce47oh

I was prescribed 25 MCG tabs of levothyroxine (generic for Levoxyl) by my MD for my hypothyroid. (I was tested at a 4.5 reading -- just below a normal 5 reading). After 60 days of taking levothyroxine EXACTLY as prescribed (i.e.; on an empty stomach, 1st thing in the morning with a glass of water; no vitamins for at least 4 hrs afterward), I started to have symptoms that I've never experienced before: my hands began hurting so bad with joint pain; my lips felt numb; and I was sweating more than I ever had in my life. I decided to stop taking the medication due to these symptoms, and in about 7-10 days from stopping, ALL these symptoms had disappeared and have not returned to date. I relayed this information to my MD who told me that my symptoms had nothing to do with Levothyroxine and that I needed to continue taking the drug. It's more than strange to me how some MDs will not listen to his/her patient -- even more so now that I've read other info on the internet where many other people have had these same side effects taking levothyroxine!! On my own, I am now looking into taking an all natural alternative that I found on wellness resources called "Thyroid helper". I will not take Levothyroxine again if I can avoid it by taking an alternative. Has anyone else out there had success taking "Thyroid Helper"?

Boy! It is funny how all of us posting here have all these side effects and the doctors for the most part say nothing or keep an eye on it. I to have symtoms ranging from bad headaches, the tickle in the throat and cough with it, to lower neck across shoulders the pain is intense. I was started out with a 20mg dose and on july 2007. There are differences with me as i have a hard time now getting to sleep. I toss and turn most of the night. It is now mid september and the doctor has never called to ask how i was doing. My blood pressure has not gone down but up. ranging from 174/110 on sept. 9 to 158/104 on sept16 2007. so i am taking myself off this crap and doing something different if only what are for-fathers did most of the time........they lived with it. Any thing has to be better than this.....thanks for all your help!

II have been on Statins for many years. Started with Zocor which caused two large muscle knots in my side. I talked to my cardiologist and was told it couldn’t be, as it would be more systemic. I asked him for a CPK check and he telephoned me and said get off of it at once. In the meantime I broke two ribs swinging a golf club. I was switched to at least three other Statins with the same results, muscle pain. I finally ended up on lipitor. My CPK was elevated, but my cardiologist said that the benefits of 10 mg. of Lipitor trumped the slight CPK elevation. All went well for a couple of years. During that time I participated in a Lipitor study and was monitored for approximately six weeks. Results were Ok until the dose was increased from 10 to 20 mg. I was immediately dropped from the study. Three weeks ago my cardiologist increased my Lipitor to 20 mg. and added co Q-10 300mg. It took four weeks until I developed severe muscle pain in my lower back and shoulders and neck. My doctor will not accept that Lipitor is the cause. I took myself off of it a week ago. I am now almost pain free. He appears to be avoiding communication with me. He also was one of the Dr. participating in the Lipitor study. I would hope that many MDs read this entire list of problems attributed to Lipitor.

In July my doctor recommended I try Yasmin to help clear up my acne. At first I thought Yasmin was absolutely wonderful! My face cleared up and due to Yasmin's diuretic effect, I no longer suffered from water retention. By the time September rolled around, my body was a complete and absolute mess. I suddenly developed severe IBS after never having experienced digestive issues. I was constantly bloated and constipated. Besides the IBS, I also experienced insomnia, anxiety, fatigue, weight gain, depression, and overall I lost my "glow!" I just looked and felt horrible and I felt like I was on speed even though I gave up caffeine.

I went to one doctor after another and they told me I needed to eat more fiber to cure my IBS. Since I have always doctors know more than me, I added more fiber to my diet and just got more bloated. One of the doctors I saw wanted to put me on anti-anxiety medication and anti-depressants. Not one of my doctors ever discussed a possible correlation between Yasmin and all my health problems.

All of my issues compounded and by January, I just had to stop taking Yasmin out of desperation because one night my anxiety was so bad I thought I was going to have a heart attack. Once I stopped taking Yasmin, my anxiety immediately went away.

It's been 3 months since being off Yasmin and I am finally regaining my energy, starting to gradually lose weight, and feeling like myself after feeling completely down and out about life.

I am not a doctor but from the research I have done, I think Yasmin caused a major hormonal imbalance and as a result my body became estrogen dominant. This is just a hypothesis but I had all the symptoms of estrogen dominance (weight gain, extreme fatigue, hair loss, depression, etc....).

This whole experience has taught me two very valuable lessons: 1) Do not start taking anything foreign until you do research and know the side effects 2) Respect MDs for their book knowledge, but know they are not always right. Do research on your own because you know your body better than anyone. Having an MD say you need more fiber in your diet or you need a prescription for sleeping pills, anti depressants, ect...is not always the best or healthiest solution.

If anyone else has experienced what I have due to Yasmin, my heart goes out to you. This past year has been the one of the worst years of my life and I will never take birth control ever again. Hang in there and know your health will be restored once you stop taking birth control.

Persistant muscle cramps.

I'm 66 years old and have a long history of muscle cramps after physical excertion such as tennis. I've been on 10mg for several years so even though the cramps have gotten more frequent and more persistant (harder to walk off) I did not think Lipitor could be implicated.

At my MDs suggestion I have stopped taking them. Surprise! No more cramps. And I am playing tennis especially hard to try to bring them on. But nothing.

This has been a surprise. I should go back on Lipitor to test that it is really the cause, but that dedicated to science I'm not.

I have been treated for HTN for the past year (I am 47) and have had great blood pressure results with Lisinopril, but I also developed the horrible cough.

I first started lisinopril first in February of 2005 but noticed the development of a terrible, gagging, cough that made it difficult for me to communicate at times (I am an RN). I would feel fine for a while and then start in with the cough...even the MDs noticed it and asked me about it at work.

I was hoping that it was just a winter cough thing since my BP was really doing well on the 10mg of lisinopril, but with my stress incontinence problem and the lost nights of sleep, and daily coughing-gagging fits, I had to stop it after a few months. I noticed that the cough subsided within a few days after stopping the drug.

My MD started me on 25 mg. HCTZ which lowered my BP although my diastolic was sometimes higher than he liked it.

I had been taking HCTZ until two weeks ago. After getting a few too many BPs in the 140/90 range, I decided to stop taking it and restarted my lisinopril. I felt okay for a day or two and then COUGH, COUGH, GAG, RETCH....all over again. I know it's the lisinopril now. I can't handle this coughing, I do groups in a mental health facility....I can't make it through them sometimes, I also have a horrible time with my stress incontinence because of the coughing.

I just restarted my HCTZ today and hope to have shaken off this cough within a few days. I see my MD in three weeks and hopefully we can work something else out. I was very disappointed in the lisinopril since it is very cheap and got my BP to a nice 120/78 range.

Well... let's see if anyone here can help us clear this mess out.

First I should mentioned that my girlfriend was diagnosed with polycystic ovaries and did not get her period for over 18 months, which her MDs kept saying was normal(???!!!!) It was definitely not normal. I took her to an excellent OB/GYN and she did some tests on her and put her on loestrin fe with the 21 days of BC and 7 days of IRON tablets.

Her MD left the practice to teach... so she was left with no MD. In the meantime, About 2 years ago, my girlfriend started to experience heavy bloating, constant urinary tract infections, decreased interest in sex, soreness during sex, etc.

She went to see her MD and they kept telling her to use METRO GEL, I believe it's what it's called, and DIFLUCAN, etc. You name it, they gave it to her. She even got tested for ALL STDS and I did also to make sure I didn't have anything I would keep giving to her.

Anyway, her MD put her on YASMIN because he said it would help out with all these symptoms. Well her sexual appetite has diminished even more and now she has vaginal dryness.

The problem is that overall, this pill has done more good than it has done bad. But has anyone continued taking the pills but been treated for teh vaginal dryness?

Please get back to me.

Thanks!

Amazing stuff at this site. I have rheumatoid arthritis and am taking Pred, which acted like a miracle, stopping my excruciating joint pains and enormous fatigue. But even at the low dose of 5mg, I had frightening mood changes, irritibility, suicidal thoughts, reclusiveness, wanting to hide, and difficulty with abstract thinking. I reduced to 4mg, then to 3mg and suddenly I have returned to normal. I have much more energy, and the mental/emotional symptoms have gone. Prednisone is very powerful drug, but one that should be used with extreme care. My MD did try to bring down the dose as much as possible. My impression is that many MDs are prescribing much too much.