I am sorry for your issues. The contrast is not as safe as people think. That is why they have all the paper work. I buy a gallon of water when I have contrast. I drink it all as soon as possible after contrast. Surgery would be risky and that is what they used to do.I have had 8 MRIs with contrast and at least 8 CT scans with contrast with no problems.
Alex
Went into hospital to have gall bladder, ovary and cyst removed. Surgery was successful and went home two days later, day after being home the vomiting started and continued for a whole day. My husband too me back to th era where the re admitted me to see if something had been nicked during surgery. I couldn't keep anything down...motion and even smells made me sick. They were stumped so they had me drink the drink like always before the test of which I told them I wouldn't be able to keep it down, and I didn't to have the MRI. Long story short, from being dehydrated from vomiting so much then getting the contrast dye, it killed my kidneys making me gain 20lbs
, lungs filled with fluid, had to have renal dialysis Four times, fluid drawn off my lungs and so many more problems. Was in the hospital almost a month.
HI -
This is a very old thread, and some of the information we're seeing comes from unsubstantiated sources or is anecdotal . We'd hate to spread fear and misinformation. If anyone wants to talk about this issue and has updated, valid scientific data (pro or con), please start a new thread.
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NO MORE POSTS, PLEASE.
I too have been poisoned by Gadolinium contrast that is said to be safe. I am having brain fog, fatigue, muscle sharp pains, arms legs, and now tingling. together with unexplained bruising. Please stay away from this contrast unless your life depends on it. had the MRI done 2 months ago... have a long way to go to detox it from system. I hope i win and it doesn't get worst.
dear Suki
can you kindly let me know the site for support? You mentioned that you live in UK. What your experience? Would you be prepared to let your case and mine go public?
To everybody on this forum, if you live in uk, please sign the petition against the use of gadolinium in hospitals.
People with normal kidney function are having serious symptoms after gadolinium and this is not being recognised by the medical communities in our countries. You need to find your way to a support group for GASF-NSF where others will understand what you are suffering.
I had mra Dec 3 and had the mra because of weight loss, tachycardia, dehydration, feels like cannot drink fluids without feeling like cannot breathe, and my heart would race after eating. After the mra I read all about the nsf and kidney damage on different sites. They gave me come to find out .04 mmol of the gadolinium . I am very freaked out for one I have protein in my urine which could be from dehydration. And I now itch all over 2 weeks after the mra. I feel depressed all the time, I also have a pigmentation mark on my white of eye . Concerned went to eye doctor and she seen a yellow raised spot on the white of my eye. She did not know what nsf is but said she would of guessed it to be some sun damage . Where did the pigmentation come from isn't that an nsf symptom ? I am 42 down to 101 pounds because of not eating much . My g f r two weeks after mra was greater than 60 . I am just freaked out and doctors look at me like I am nuts I am vitamin d deficient, vitamin b deficient, iron level very low at 37 . An anemic so I am wondering if the itching can be from that or do I have nsf ? I feel nervous a little like I cannot sit still I don't know if that is from always worrying if I have nsf or does that dye mess with the nervous system. Why did they give me such a high dosage .04 mmol or 40 cc isn't that extremely high dose ? Thanks to anyone that can give me feed back. This all started actually with the lost of weight back in august when I had ct scan dye then 2 days later became very nauseated so gave me another ct scan more nauseous then dealt with it lost weight then that's when had more trouble and mra Dec 3 now the itchy and short of breathe is driving me nuts ! I know short of breathe could be low iron and anemia I hope and not my organs hardening from nsf. I feel a mess !
Hi there
I had a MRI scan in April this year. The nurse let 2-3 ml of dotarem going into my tissues at a principal teaching hospital in london south east.
I had no immediate reaction, but 2 days later a little dizzy, then my upper arm had a bruise at the site of the injection and a burning pain, which strted in the scapula and rotary cuff. My kidney were normal prior and and after the injection. I went straight to the toilet after the injection, but oculd not go again an hour later, although it became normal as soon as I had a couple of glass of water. 0 days later I started to feel again dizzy, nauseated and crawling pain all over my body. I had a blood test almost a month after the injection, which showed no damage to liver, kidney or thyroid. blood count all normal. I started to feel quite alarmed and went to A&E of the main south east london hospital. the doctor said I may have a trapped nerve. A week later as I felt rather bad and also suddenly depressed, I saw my doctor who reassured me the symptoms would go away. However I developed sudden bruising, even my eyes are itching, my head and face. Before the MRI I had a sort of itchign around my breast which went aroudn my neck and back as well, due to hot weather. Doctor said it was a sort of fungal infection, but 6 days later when I went for the scan, it was gone. I have been in touch with the radiologist who tried to reassure me, but as I said they werenegligent to let some liquid into my vein, they do not wish to communicate with me anymore. I have also contacted the drug manufacturer who is analysing my simptoms but no one is doign any test. I am feeling very down, becuase everybody thinks I am worrying so much that at the end I will feel the symptoms of this NFS diseases as a sycomatic reaction. I am taking vitamin B complex which has helped a bit. My diet is excellent and I have no health other problem.
a week later
Thanks everyone, this is behind me now, I am no longer worried about it, thanks for the information!!
You need to put this into perspective. I saw my neurologist last night in the UK. I told him about the concerns and problems with Gadolinium in the USA he was most surprised and has NEVER HEARD of it or a problem with Gadolinium, and all the years of using it etc has never heard of anyone getting ill or even having NSF.
I think sorry to say this, USA has become a suing culture and only one person needs to have got NSF after having an MRI with contrast and bingo everyone is getting it.
NSF is a stand alone illness NOT CAUSED by Gadolinium in general. The only reason why someone having Gadolinium COULD possibly rarely get NSF is because they would have renal failure or severe kidney problems, so the kidney cant flush out the Gad quickly enough and the longer it stays within the body the more chances of someone MAYBE having a problem. There is no proof that Gadolinium causes NSF.
If you GOOGLE systemic fibrosis or NSF YOU will find tons of websites all about it and the majority of the web sites are LAWYERS trawling for customers.
Did you get any medication for your cellulitis?
Like I said in the UK it isnt even a problem. Please try to relax over this you will make yourself ill. Like others have said perhaps the burning and aching in the legs is part of the reason why you saw the GP in the first place?
Anyone get killer headaches in the 24 hour period after MRI? I am not worried about it I just wonder if it is just me.
Alex
I went to the Dr. about my leg pain since one area was red this morning. He doesn't know what it is, called it cellulitis, said he doesn't know what caused it but is pretty sure it is not NSF, was surprised I even knew what that was.
I am wondering though if he doesn't know what it is or what is causing it how can he know it is not NSF exspecially by his own ommission he has never saw it.
Thank you and yes, I have some health anxiety, am I that transparent?
Hi, I'll try to relieve your mind. I was puzzled that the warning on Gadoliniuk included liver disease, because in all of my reading about NSF I had never seen anything about it.
I finally found the link. People with severe chirhosis of the liver or with sever liver failure (this means very sick people with their liver disease) sometimes develop a secondary type of renal failure. This is called Hepatorenal (liverkidney) syndrome. These people with hepatorenal syndrome are deathly ill. The kidneys really have nothing really wrong with them, but the shutdown of the liver also shuts down blood flow to the kidneys and they begin to fail.
So, if your elevated bilirubin is not due to severe liver disease, you are not at risk for NSF. NSF has never been seen in someone with kidneys that are working well. In fact, the decrease in kidney function must be pretty significant to put you at risk.
I don't see that you have ANY risk at all for NSF, but remember I am not your doctor. This is not the place to make the final determination of that. NSF is very, VERY rare! All of the cases have been in renal failure of either a moderate or a severe degree and most have already been on renal dialysis.
I think you need to get some help for your anxiety. Do you tend to develop these fears about health issues? If so, it can rob you of all of your piece of mind.
Take care and relax.
Quix
Great info to add here.
If you remember I'd posted about how my contrast mri had made me tired afterwards; it happens after every contrast mri I've gotten, but never with normal mris. Just an afterthough, no response needed. :P
Dear scared,
I'm sorry but I can't be of anymore help with this question - perhaps someone else out there can add to this. I've not done that much research even though I have had contrast three or four times this year with testing. I'm not concerned about the side effects because my kidneys are fine. It seems to be people who are already experiencing severe kidney problems who experienced these side effects.
How did you learn about NSF and why are you so concerned that you have it? Perhaps those answers will help someone else here with some clues about your legs.
rest easy,
Lu
Sorry, guess I have to post again to click add to watch list, It got removed some how.
My legs are burning, that is what is bothering me most! I am terrified, I have had my kidneys checked since the MRI and they are still OK, can I get it with working kidneys?
I looked at the Magnevist page, the manufacturer is Bayer, and it says that NSF can be diagnosed by deep skin biopsy and histopathology. That sounds rather painful - I would wait it out unless you really feel you have to know if it is or isn't NSF.
From the Bayer website - "Symptoms of NSF may include thickening of the skin, swelling of the lower extremities, redness, pruritus, and burning sensations." From what you have said, there appears to be no reason to believe it is.
I hope this helps,
Lulu
I was having twitching in my face that could not be explained, so I had a brain MRI, didn't find anything. I do know they used 13CCs of Magnevist (sp?)
Hi Scared,
I would say no, you are not at risk for NSF, but I am not a medical authority.
There are these persistent concerns about NSF and contrast that are so unfounded, but seem to have a life of their own and won't go away. If you have doubts about this, please talk to your doctor for reassurance.
You don't say why you had the MRI, but I would assume there was already a problem there to be looked at. Can you tell us a little more? Those reasons for the MRI may well be linked with the problems of your legs. I don't have a guess about the spot on your eye.
Also, 120/80 is an acceptable blood pressure range. It is not high, although you are bordering on the prehypertensive side. Hypertensive blood pressure (high) numbers would be 140/90 or higher.
I hope this helps with the anxiety - please tell us more about yourself and let us know how we can help.
my best,
Lulu
If you have a high bilirubin, but no other liver problems
and your kidneys are working fine are you at risk of NSF?
I am terrified I have contracted NSF after MRI with
contrast, my legs have been bothering me and I have a raised spot
on the white of my eye. I also have high blood pressure,
about 120/80. Thank you for any information you can give
me
Frankly, I would rather have the Gad as a contrast than the radioactive isotopes, or the IV iodine, both of which I have had several times for tests. I have reduced kidney function 65% from surgical procedures, and am not worried in the least. At this point in my life, if I am urinating, my lidneys are working, and that's a good thing LOL
This has been a great discussion, and I have enjoyed every bit of it! Thank you for all of the information. I love this place! I may not write often, but I am lurking!!
Cydney
To Quix & Heather,
Thank you for this very informative discussion. I must admit I was a little worried about the die when having my MRI.
Now I have been given good info and know the facts.
That's what makes this forum so important to all of us. Lively discussions that get down to the truth of the matter, and increase our knowledge.
doni