April 23th
2009
11:11 AM
I started Lipitor 2 months ago, today is April 23, 2009.
1 month ago I started with Vertigo, doctors have tried many things to get rid of it but can't.
! week ago I started having trouble breathing, talking very short walks, problems still with vertigo, pain (headaches) on my left side, and I never have had headaches, pain in my neck left of the c-7 vertebrae.
Now 2 days ago I have problems swallowing food in the center of my chest, it really hurts, so now I am on an ice cream diet to figure things out.
I went to my doctor yesterday due to all my problems, which are all new in the past 7 weeks, and she did an x-ray, and blood work thinking I had a blood clot in my lungs.
At 6:30 pm last night 4-22-2009 she called me to go to the emergency room and have a cat scan done, and the results were I am loaded with lip-nodes in my chest and arm pits, and it look like cancer, so I have an appointment today at 2:00 pm to see what the plan of attack is.
God Bless,
L. G.
Biddeford, Maine
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-- By lennygauba | Reply | (1) replies | Private Message me
March 14th
2009
9:53 PM
I have been on 10 MG of Lipitor for almost 3 years. Since I began taking it I have had recurring issues with an anxious feelings, my lower GI is constantly churning and I feel like I am stressed out. I have a low stress job, a stable happy family life and yet I feel nervous all the time. I sleep for 3-4 hours and then wake up and am unable to get back to sleep. I have been forced to take a nap ever day after lunch just to get through the day. Additionally, I developed tremors in my hands and was diagnosed with something called Benign Essential Tremor and put on another medication to control the shaking.
Yesterday I decided I had enough of this and went to see my cardiologist to discuss the symptoms. I stopped taking the Lipitor on my own 2 days before. The doctor told me that none of my symptoms were related to Lipitor! I replied that I was convinced that they were all in fact caused by this drug. He suggested I stop taking the statin for 2 weeks and see if the symptoms stop. I am now on day 4 without lipitor and am already feeling less anxious.
I went to the Nuerologist 2 weeks ago and got her to discontinue the anti-tremor medication. I am going to get all this crap out of my system and hopefully get my life back.
-- By jeffracer | Reply | (5) replies | Private Message me
September 3th
2008
2:21 PM
I have muscle pain, weakness, and chronic lower back pain. Started statin drug, Simvastatin, on 11/21/07. I take no other drugs. Within two weeks, I could not sit without severe lower back pain. Reported problem to family medical doctor on 1/11/08. M.D. sent me to physical therapy for 8 sessions. No relief from physical therapy so I requested an X-ray on 3/20/08. X-ray shows very mild degeneration at one lower vertebrae. M.D. sent me to an orthopaedics doctor who recommended continued physical therapy. Went to a Chiropractor instead. After six chiropractic sessions with little relief, I made an appointment with an Osteopathic doctor. My M.D. sent me to a rheumatologist who prescribed high dose naproxen for two weeks. The rheumatologist ordered and X-ray of my lower back area. The lower back X-ray produced no negatives. The rheumatologist's next step will be to order and MRI of my lower back area. The D.O. suspects statin induced myopathy and because of hyper reflexes he ordered an MRI of my brain and cervical spine. I am now recommended to a neurologist who specializes in the diagnosis of multiple sclerosis. Am I getting the run around? Only one doctor said I might have statin induced myopathy. The rest will not even mention the statin drug theory. I just pray for ache and pain relief. I have some improvement after four months off of the statin which I believe is quite a strong point that it was the statin drug and not some unknown condition. I don't think arthritis or MS conditions improve. All I know is that I had no health issues before taking the simvastatin. Good luck to everyone who has or is taking a statin drug. BEWARE!!!
-- By pdsdenver | Reply | (4) replies | Private Message me
August 16th
2008
1:49 AM
Initially, numbness and tingling in extremities which subsided, but memory loss and loss for words is very uncomfortable, and my neurologist suggested caffeine every AM to compensate, which helps some, but not enough. Difficulty reaching orgasm has become very frustrating as a side effect, but is better than the horrible headaches every day. What a choice!!1
-- By amlooney | Reply | (1) replies | Private Message me
June 11th
2008
2:50 AM
I have been taking Topamax for about 6 months now. I have been on several different everyday medications for migraine prevention and Topamax has been the best one. I was first prescribed Relpax to help relieve the headaches. I eventually got to a point where I was getting migraines every day/every other day (insurance only covers 12 pills per 20 days). I was later switched to Imitrex - which is MUCH more effective (1 100mg tablet) but my insurance only covers 9 pills per 30 days (unbelievable).
Just wanted to give you guys some background on my situation. I have been through 2 MRIs and a CAT scan, visited a neurologist, done 2 sleep studies, spent 2 months on a breathing machine for possible sleep apnea causing migraines. My family doctor, my neurologist, everyone I saw was unable to determine the cause of my migraines.
THE GOOD NEWS is I was referred to an UPPER CERVICAL SPECIALIST by my old chiropractor. This may not sound believable but my headaches have decreased to about 2-3 per month since I've been treated by my new chiropractor. My old chiropractor was the type who did a complete adjustment on my spine/hips and cracked my neck both ways every time I visited. The upper cervical specialist focuses on C1-C2 vertebrae and uses calculated heat readings to determine where there is inflammation and there is no twisting/turning involved. Look up upper cervical chiropractic on google and see if these treatments will help with any of your headaches. It has helped my situation dramatically and I will continue seeing this specialist and probably come off of the topamax in the next few weeks.
-- By legacygt48 | Reply | (1) replies | Private Message me
May 26th
2008
8:46 PM
I had minor cramping when I first got the Mirena put in. But, it was much milder than when I get period cramps. I didn't have any trouble with it (unless you count extremely light periods as a bad thing) until I did air travel (cross country airplane flights). Now, keep in mind, I travel a fair amount by car & have had zero Mirena issues from sitting in a cramped position for hours in car travel. Flying on the airplane caused really weird lower back cramping that put my out of a lot of activities. It was quite definitely core muscles cramping severely, to the point of pulling my lower back vertebrae & tailbone slightly out of alignment. After 3 weeks of pain, I finally went to a chiropractor & got realigned. This has happened with 2 flights thus far out of 4 (it doesn't seem to happen on short 1 hour or less flights). I have NO idea why this happens. I normally have no issues when flying. The mirena is the only thing that's changed. I can only assume it's the combination of the position when in a plane seat for so long & the mirena. Maybe it's poking one of my fibroids in that position?
Mirena has had zero effect on my PMS. PMS is just as bad as without any BC. My acne is just as bad as it is w/o BC. I guess I need Retin A & Midol. LOL
Things to keep in mind when reading the above: I've never had a child. I've been pregnant once & miscarried. I'm in my early 30s. I'm a light smoker. I have uterine fibroids. I rarely drink. I have lupus. Some of these things may or may not have an effect on what happened to me. So, keep that all in mind.
Also, as with all of these experiences, keep in mind it's personal experiences & we're all unique individuals. I'm keeping my Mirena because this is the only big issue I've had & I don't travel a lot.
January 29th
2005
7:38 AM
I've had severe-debilitating allergies for thirty-four years. About 15 years ago I started taking kenelog shots 2-3 times per year. (Once I had the discolored indentation in my hip as described by the postings here. It took a long time (year+) but it did finally go away. )
My concern now is that I've been diagnosed with degenerative spine disease, it's similar to arthritis-- basically my vertebrae are deteriorating. When I received my CAT scan at a military hospital they asked me if I had been jumping out of planes... I have no family history for this problem, nor have I ever been in any kind of accident that could lead to this. A long time ago I remember someone telling me that she had to have a hip replacement at an early age and she thought it was linked to kenelog use. Any other long time users have bone deterioration problems?
-- By bynco | Reply | Private Message me
July 16th
2004
12:07 PM
I have diagnosed osteoarthritis, two joint replacements, looking at a third, and my knee hurt at time. Bad fall over a year ago led eventually to spine surgery with fushion of several vertebrae. Before fall I had some back pain and have had the shoulder pain for years(and now requires partical reaplacement). I was very active and relatively athletic doing agility with my dog. After fall and sugery for pinched nerves, I have never felt normal. Too much pain all over, fingers still numb, don't feel safe running with my dog. I suffered muscle degeneration due to the pinched nerves. Finally after numerous expensive test etc, rheumatologist suggested kenalog shot if I didn't feel better soon. Also tentative diagnosis of gout but my stomache could not handle pills for gout. So I got a shot of kenelog. - Super! I felt "normal" for the first time in over a year, didn't feel weak in knees, felt I could walk faster and further. Positive side effect was clearing my sinuus' and clearing up cough from phlem from sinus area. Got shot about 5 weeks ago and it has gradualy faded. I do not feel as painedl, but my activity level has decreased. I want another shot.
-- By dreampax | Reply | Private Message me
Kenalog (3) Lipitor (2) Topamax (2) Simvastatin (1) Mirena (1) Neurobion (1) Inflamase Forte (1)
June 4th
2009
2:33 PM
I have had a total of 5 kenalog injections in my back for no disk left between two vertebrae, doc says fused naturally and no movement. I still have pain. I am scheduled to have yet another shot in the neck area, 5 bulging disks causing pain around the shoulder blade. I have less sciatic pain, but I have HEADACHES for the 3 months since the first shot, they don't go away. No OTC pain relief works for these headaches. The doc says the kenalog does NOT cause headaches, I know these guys lie or don't care about the FDA list of side effects. I am hesitant about getting another shot. He wanted me to have this one done under sedation, I declined, since I had the others without. He said more sensitive area and don't want you to flinch. I also get, I assume kenalog injections in both feet for morton's neuroma. Left foot shot worked. Right foot 3 shots and still hurts and numb, they can't seem to get it right. I am tired of getting the shots, and today I went to that pain management doctor and forgot to ask him how long can I expect the shots to help the pain, years? months? or weeks. I barely do anything anymore, afraid to bend, or even move. I had to go to ER first time for my back on 2/14/09 and sent to different docs and finally pain management. For those of you whose docs don't order an MRI for you, I wouldn't have the shot. I had and MRI of the back and neck and this doctor gives the shots while I lay on a fluoroscope table, I can see on the screen in front of me where the doctor is injecting. Hit and miss without an MRI is just not medically correct. Good luck to all and gonna think about whether to get another shot next Thurs.
-- By manchesternjgirl | Reply | Private Message me