Headaches after CCSVI
Headaches after CCSVI
I had the balooning in Frankfurt on 25th June and at first I helt a lot better and had lots of improvements. I have had really bad headaches the past 5 days and I am worried that this means that there are new lesions because it feels really odd. Can anybody help or has anybody had the same?
Thanks
Verity
Thanks
Verity
- costumenastional
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Are you on any anticoagulants? Some of them (Plavix for instance) can make you feel like that.
There is also a chance for your headaches to be caused from altered blood flow inside your skull.
I wouldnt worry too much except if you were experiencing headaches before the operation. Only then you should be thinking of restenosis so early.
Anyway, contact your doctor please.
There is also a chance for your headaches to be caused from altered blood flow inside your skull.
I wouldnt worry too much except if you were experiencing headaches before the operation. Only then you should be thinking of restenosis so early.
Anyway, contact your doctor please.
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I dont think because i dont really know. But even if i knew, i cant prescribe drugs to you ;)
What i think is that you should have a little talk with the surgeon who operated on you asap on this matter. Most doctors prescribe drugs just to be on the safe side. You dont need a clot or something. But your doctors is the one to decide.
I am on Plavix for 3 months and aspirin and daflon for six.
Personally, i d take whatever is happening to you as a sign that the treatment really changed something that had to be changed, you know what i mean? I really dont think that it ll be like that for ever. Try to rest and give it some time. Things are now different inside your brain.
Hope it ll help your MS to subside.
Many of us have experienced weird stuff post op, believe me. Stay calm and let us know when this resolves. Because it most probably will.
WHATEVER YOU DO, KEEP YOUR DOCTOR INFORMED AT ALL TIMES.
What i think is that you should have a little talk with the surgeon who operated on you asap on this matter. Most doctors prescribe drugs just to be on the safe side. You dont need a clot or something. But your doctors is the one to decide.
I am on Plavix for 3 months and aspirin and daflon for six.
Personally, i d take whatever is happening to you as a sign that the treatment really changed something that had to be changed, you know what i mean? I really dont think that it ll be like that for ever. Try to rest and give it some time. Things are now different inside your brain.
Hope it ll help your MS to subside.
Many of us have experienced weird stuff post op, believe me. Stay calm and let us know when this resolves. Because it most probably will.
WHATEVER YOU DO, KEEP YOUR DOCTOR INFORMED AT ALL TIMES.
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Hi Vee1012,
I developed terrible daily migraines after my transverse myelitis (lesion c3-c5).
Immediately after the angioplasty these migraines went away. However, I had a weird throbing in the head that lasted for a couple of days. I had experienced that weird throbing days after my last MRI, and my neurologist could not explain why.
Well, my vascular surgeon told me that the weird throbing was a related to the contrast used in the venography (and also used in MRIs). He also told me that the throbing was going to stop days later.
I just drank plenty of liquids. I did not take aspirins as the throbing did not cause pain or major discomfort. You should inform your vascular doctor and ask what to do.
I developed terrible daily migraines after my transverse myelitis (lesion c3-c5).
Immediately after the angioplasty these migraines went away. However, I had a weird throbing in the head that lasted for a couple of days. I had experienced that weird throbing days after my last MRI, and my neurologist could not explain why.
Well, my vascular surgeon told me that the weird throbing was a related to the contrast used in the venography (and also used in MRIs). He also told me that the throbing was going to stop days later.
I just drank plenty of liquids. I did not take aspirins as the throbing did not cause pain or major discomfort. You should inform your vascular doctor and ask what to do.
headaches
Headaches have gotten better since procedure. I got 2 stents on left jug and am on Plavix for 3mos I am glad I got stents so don't have to worry about restenosis
Good Luck
Good Luck
Mino/Copaxone, IVIG
LDN, Prokarin
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LDN, Prokarin
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Dr. Sclafani said:Interrupted wrote:Erm... care to elaborate??concerned wrote:Stents can cause iatrogenic stenosis and might be dangerous.
2. stents have the risks of in-stent stenosis leading to loss of the vein completely...certainly do not want to put one there for a physiological distensible narrowing
Somewhere else he used the word iatrogenic, as I have many times in talking about the risks of this procedure.
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Expect Headaches
I would expect headaches after balloon venoplasty. As you have altered the blood flow through the CNS the brain will react. Our brains do not have many sensory nerves, they are unlike our skin. Pain is the basic sensation of something happening in the brain, it is a defense mechanism to damage.
A headache will not tell you if you are experiencing a positive or negative impact from de-stenosing your veins. My advice is to drink lots of fluids and keep off alcohol and caffeine. Paracetamol may be used if the pain troubles you. Do not use Aspirin or NSAIDs (eg Ibuprofen) as they may interfere with your blood thinning drugs. If the pain is severe or intense in one area, please contact your Surgeon/Radiologist who performed the venoplasty or your family doctor.
Kind regards,
MarkW
A headache will not tell you if you are experiencing a positive or negative impact from de-stenosing your veins. My advice is to drink lots of fluids and keep off alcohol and caffeine. Paracetamol may be used if the pain troubles you. Do not use Aspirin or NSAIDs (eg Ibuprofen) as they may interfere with your blood thinning drugs. If the pain is severe or intense in one area, please contact your Surgeon/Radiologist who performed the venoplasty or your family doctor.
Kind regards,
MarkW
Mark Walker - Oxfordshire, England. Retired Industrial Pharmacist. 24 years of study about MS.
CCSVI Comments:
http://www.telegraph.co.uk/news/health/8359854/MS-experts-in-Britain-have-to-open-their-minds.html
CCSVI Comments:
http://www.telegraph.co.uk/news/health/8359854/MS-experts-in-Britain-have-to-open-their-minds.html