Heavy legs symptoms and conditions

Hi I am dumb struck by coming across this site i never dream it could be my mirena causing my unexplained symptoms but the more an more i read it i am fighting with my hospital to get it removed A.S.A.P. i have suffered severe dizzy spells,heavy legs,fatigue,sweats,headaches,loss of concentration,mood swings,bloating,thinning of hair,weight gain, depression,dont want to communicate,just fallen apart in the last 17 months,had number of tests all come back normal,i been back to hospital today to fight this corner an they need to see how many women this really affects as every doctor i have seen says no way can it be the mirena but reading all these this needs looking into.i am worried about the dizzy spells they are my most concern along with panic attacks that come out of the blue..makes me think it may be my mirena after all :( just want to be back to my old self again..i have been to A& E at least 9 times with same symptoms only to be put on diazepam which i don't like to take,i am so upset that i still got to wait 6 weeks+ to have it removed as i got to go under to have it done as they cant reach the threads they are up instead of down...i am hoping after my long wait that i have now found an answer to all my symptoms an the mirena needs to be looked into more.an after it is removed i hope i get better as i have also read it can have after affects.nightmare wish i never had it put in.....

I start taking Yasmin 2 years ago,and discontinued it because of the melasma that I got on my face.Now that I am reading all this posts,I am connecting dots.I had been having horrible headaches,feeling bloated,very tired,depressed,rapid palpitations,chest pain,heavy legs and varicose veins.I never thought it could be caused by the pill,I really thought I was because I was aging(Im 32)Now I know the reason.As soon as I stop taking it all the symptoms stop too.Now I have been feeling great,but I was attributing to the fact that I start taking organic apple cider vinegar, MSM and some more vitamins.

IF YOU FEEL/EXPERIENCE ANYTHING ABNORMAL FOR YOU OR DO NOT FEEL QUITE YOURSELF SEE YOUR G.P./NURSE AND SERIOUSLY CONSIDER GETTING THE MIRENA COIL REMOVED
This medication may be suitable for some people but if you experience any of the following, I urge you please, please please, 'demand' that you want the Mirena removed. My symptoms were noticeably worse around my time of ovulation. I've also found out that people previously treated for/suffering from depression should not be prescribed this medication. (I've been on Prozac in the past). I had it fitted in Aug 2007 to combat very heavy periods and severe PMT at the recommendation of my G.P.and had it removed Sept 2008. Symptoms I experienced :-

Dry/furry mouth
Headaches (over time these became migraines)
No concentration
Poor memory
Lethargy (constantly tired and drained)
Smelly discharge (still noticeable straight after washing)
Very heavy legs
Numbness in my legs
Joint pain and clicking (mainly in my shoulders and knees)
Developed facial hair (mainly under chin and jawline)
Hair loss
Weight gain around my stomach (without increasing my food intake)
Feeling constantly bloated.
Spotting randomly for duration of Mirena being fitted. (Brown spotting)

Panic Attacks ( awoken in the middle of the night with them) escalating to the following:-
Palpitations (for no apparent reason)
Clammy/sweating palms and feet
Aggitation ( during an episode if someone was talking to me I wanted to really yell at them 'Just shut the **** up! You're doing my head in!)
Feelings of madness (actually wanted to run away from my own mind)
Pins and needles/Tingling in my hands and feet
Electric shock like surges going through my body (my nerve endings were obviously suffering)
Muscle tremours/shaking (mainly arms and legs)
Eyes became extremely light sensitive
Heightened awareness of sound

Insomnia
Terrible nightmares
Depression
Feelings of detachment from the real world.
Visual disturbances
Episodes of blurred vision

These symptoms did not appear straight away but appeared gradually and with more veangance the longer I had the coil. The more concerning episodes I experienced happened after about 3 months and very erratically. I could not predict when or what time of day I was going to have an episode or pinpoint any reason for bringing on an attack. I had no control over the effects, was absolutely petrified when I experienced a panic attack and just had to ride it out.
All my G.P. did was prescribe me anti-depressants to which I reacted badly. Blood tests also failed to show anything abnormal.
I even tried herbal medicines as an alternative and experienced similar reactions to the prescription drugs. I've now become very pill-phobic and would rather ride out and get over symptoms myself. Paracetamol & Ibuprofen being the only medicine I trust to take now. I had a horrendous year and everyone suffered. Not only my family, but I was signed off of work for 3 months. It was a very worrying time for my husband and my children, who all had to keep an eye on me and witness the effects of my symptoms. On looking back now, I don't know how I managed to function at all and even do my job. Most of the time my energies were spent concentrating on trying to appear normal and held-together to the outside world.
Although I feel 100% better in myself, I noticeably experience more migraines and headaches than I ever did in the past, along with palpitations, usually during my week before. Two days before it I often really feeI like I'm losing the plot! I also really bloat up now a week before my period, feel sick and have a feeling of being ' very full', so am hungry but don't really want to eat. One of my big toe-nails has gone black over the past few months and not through injury. This has just been sent away for analysis. The one on the other foot is raised/ridged/thick/yellow, but normal growth has resumed half-way up now, which I feel co-incides with the state of my health on having Mirena removed. The nurse I saw recently explained that it is true that nails and hair show the history of our health so, for me, this would seem true.
I wish I'd been made fully aware of all possible side-effects of this medication and am now actually concerned that the effects I've suffered may have left some permanent damage.
In spite of all this, it's so good to be me.

During my 6 months on Warfarin (Coumidin) I experienced tremendous lethargy and short term memory loss. No issues with other commonly reported symptoms of hair loss, heavy legs,…
I am a 49 year old male. In January 2008 I was diagnosed with DVT's in my right lung. Interestingly I experienced 100% of the pain on my left side though the DVT’s were on the right. The onset of symptoms was a pain in my chest like I pulled a muscle lifting something. The pain progressed from "notable" to progressively uncomfortable, where I was restless in bed to the point of not sleeping. On the 3rd day after fitful sleeping and progressively more painful breathing, I made a doctor's appointment for that afternoon. By the time I got to the Dr. I was sure I had made the right decision (I am male and avoid these things).
My primary care did an EKG to rule out a heart attack which the symptoms were identical to; sharp pain in chest toward left shoulder and arm, trouble breathing. I was sent for an X-ray and was very uncomfortable laying still on the Xray bed as the pain as I inhaled had gotten sharper. I went home and resumed office work but soon was in extreme pain with each breath. So much pain that I could not lay or sit, but collapsed to my knees where I stayed for 20 minutes until I could move again. I called the doctor's office and was advised to go directly to the ER. Duh. The ER again ran an EKG and ruled out cardiac issues.
Three ER Attendings pondered my condition for an hour or so and then began asking as series of questions and at the 3rd question – had I flown any long flights recently? Yes, several transatlantic – at which I saw their glances and was whisked off to a CAT scan which confirmed DVT’s. I was put on morphine and some IV’s and admitted for 5 days. I started Lovenox shots and by the 4th day was feeling better.
Blood tests did not revel any genetic disposition (factor V) for clots and no family history so it was recorded as “Coach Class Syndrome”. I was put on Warfarin for (5mg/day) for 6 months. I was able to keep relatively good INR’s. I came off Warfarin (12 August 2008). I will have to take Lovenox shots before long flights. I am happy to come off the Warfarin as I experienced tremendous lethargy and short term memory loss. No issues and I have been off coumadim for 6 months now. Glad to have that behind me… hopefully.

Leg pain, heavy legs, bloating, gas, back pain, headache, arm, wrist and hand pain.

I have been taking Singulair for 5 weeks and stopped after developing high blood pressure, numbness and tingling all over my body, flushing, anxiety, memory loss/difficulty concentrating, skin burning sensations, fatigue, "heavy legs" feeling, heart palpitations. I have been off of this drug for 3 days. I still have the side effects and hope that they will go away ASAP. I am also a very well-controlled 28 year old diabetic and when I had neuropathy-like tingling sensations in my extremities (from Singulair) I became worried and angry. I am seeing a doctor tomorrow for a full exam. If this drug has caused me permanent nerve damage I intend on filing a lawsuit against the drug company.

I am 42 years old and been taking crestor 10 mg for about 18 months to 2 years.. Recently been feeling tired with heavy legs.. told my doctor did a blood test everything was normal.. doctor advised to get off crestor its been 3 week and still feeling tired in legs.. am pretty active, workout , lift weights.. walk and play golf lately 18 holes carrying bag are becoming difficult.. will stay off crestor for a while and see if leg pain and tiredness goes away.. Anyone experienced similar systems... What did you do... My cholesterol on crestor had dropped to 160.. last test while on crestor was 238 hdl 133 and ldl 64.... not sure what to do but till i don't feel normal do not plan to take crestor as that is the only medication was taking....

Im a 57yr old female, when i was given Lisinopril 5mg 6months ago my doctor said it was the cleanest HBPT, around so i started taking it, i was on medication for cholesterol about 6 different ones, which made my life hell, so BP went up hence this medication, the mood swings, have been terrible, happy one day the next i hate everyone who comes into view even my husband said he cannot take this verbal abuse i send his way, i have felt so depressed, in the last couple of days i have just felt like ending it all, cant sleep, crying, all the time, headaches, coughing, heavy legs, noise in my ears, swelling of legs and fingers, i have got to find an alternative remedy, my life is worth more than feeling like this, im back to see the doctor tomorrow as i cannot cope any more, neither can my family

Found this site and read the postings for the first time today. I cried when I read the first posting because it was as though I had written it myself. I have experienced so many of the negative side effects such as, depression, apathy, loss of sex drive, crying almost every day, anger for no reason, pain, and more. I am 38 years old and have been using the ring for almost 2 years. I took it out today as soon as I finished reading other's experiences. I am looking forward to being my "old" self soon, and I know my husband and children are too.
Maybe the side effects are worse for women in their 30's and 40's versus 20's. Not everyone posted their age but I was curious regarding this possibility.

This note is regarding some measures for healing and pain relief. I have been in pain due to taking Levaquin three months ago. My pain is widespread. I have peripheral neuropathy. My whole body is tender and sensitive. All of my joints ache. It's hard to walk or sit for long. My pain is still disabling but it has improved. I thought that I would share with whoever may be interested what has helped my pain the most. I see a chiropractor every week and I also see a Chinese doctor every week. The Chinese doctor does therapeutic massage (deep tissue) and he also does acupuncture weekly. The acupuncture doesn't hurt as much as you might think. Other things that I've found that are helpful are warm Epsom salt baths and any topical cream that warms the area such as zostrix. Creams for muscle soreness may work also. I try not to take pain medication because it can just lead to other problems . If I have to take something I take either excedrin or Tylenol. NOT ibuprofen. Also, the body can't heal as quickly if it is being bombarded with offending agents. Therefore I have eliminated the following: Sodas (regular and diet), nutrisweet, msg (read the label), bleached flour, caffeine and many other things. I try to avoid sugar and I use stevia as much as possible. I have done a lot of research regarding nutrition since this happened to me. What I have come to realize is that good foods are like medicine. I have to supply my body with the proper nutrients and it will heal itself. Lots of fruits, veggies, whole grains, nuts, lean meat (I don't eat red meat). I avoid fast food and processed foods. The rule of thumb is that if nature made it it's good for you. If man made it...read the label very carefully. I hope that this info will be helpful to some of you. My prayers are with you all.

chris

I have been on synthroid for about 6 months now. Some of the side effects I have been experiencing are numerous.I have hair loss, sometimes I get so ill that no one can stand to be around me, my weight has gone up about 30 pounds, my cholesterol levels went sky high so now I'm taking Crestor, I'm bloated most times, I have episodes where my face flushes and gets so red that it feels like its on fire, and now I've just started experiencing burning and aching of the legs, I'm tired a lot too! My doctor said I would lose the weight but every time I go for check ups and get on the scale it just keeps going up. I would like to know if anyone else out there is experiencing the burning and achy legs because I have been tested for everything and they can't find out what is going on. They of course say it's not the medication.It seems to never be. Does anyone feel me??

Hi!
I have ulcerative Colitis. I had a bad flare up since Thanksgiving 07.I have been on Prednisone since the beginning of Dec.07. The first 3 days it was giving to me by IV every 6 hrs.I was hospitalized due to tremendous blood lost. After this my doctor put me on 60 MG a day. 6 pills of Asacol and I also was on ennama with Cortisone which totally almost killed me. The side effects were sooooooooooooo bad,let say I had them all.Right now I'm dealing with the side effects of the evil Pill " Prednisone" Moon face and this awful bloating in my upper abdomen, tiredness, no energies, heavy legs. It makes it really hard for me to get out & around.I hope my doctor will get me off this Prednisone. Not only messes it up your normal living no it also makes you look like a ugly bulldog! I hate it!

I am a 57 year old female. I have been on lipitor for less than 2 months. Woke up with "charlie-horse" cramps in right calf. This happened at least five times last night. Today I have a constant pain in my calf. Called the pharmisist who told me to stop taking the drug and call my doctor. I will not take this again. I developed heavy legs while on zocor so I had to go off it also. I am also very tired by the afternoon and can barely keep my eyes open. I will have to find something else to lower my cholestol.