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MRI results with two small white matter lesions - MS?!
Hello, I am a 29/M. In October I started having red/teary eye with sinus pain. PCP thought sinusitis. Later - tingling in left arm and leg, foggy state, headache on each side of head. After many CTs and MRIs and many other doctors - everything OK. Did B1, B6, B12, sinus CT, head CT, brain MRI in December, ENG in February - all negative. Finally did another MRI in March with some alarming news. Now I am freaking out because I've been referred to the MS center at UCSF. Here is the summary:
Findings:
The ventricals are normal in size and symmetric in the midline
without evidence of mass effect or shift. Cortical sulci and subarachanoid spaces are symmtric and normal. There are two tiny white matter lesions adjacent to the trigone of the right lateral ventricle, seen only on the coronal FLAIR sequence. There is no contrast enhancement of these small lesions and no other contrast enhancing lesions are identified. No other abnormal foci of increased or decreased signal intensity are seen anywhere intracranially. Normal gray/white matter differentiation.
Impression:
1. Two tiny white matter lesions adjacent to the trigone of the right lateral ventricle without evidence of surrounding edema or mass effect and not demonstrating contrast enhancement. The largest of these measures about 4 mm in size and the second measures 2 mm. These lesions are nonspecific and could represent some chronis gliosis or scarring. Early demyelinating disease cannot be entirely excluded.
2. Otherwise normal appearing magnetic resonance imaging study of the brain.
Any ideas? Thank you!
Findings:
The ventricals are normal in size and symmetric in the midline
without evidence of mass effect or shift. Cortical sulci and subarachanoid spaces are symmtric and normal. There are two tiny white matter lesions adjacent to the trigone of the right lateral ventricle, seen only on the coronal FLAIR sequence. There is no contrast enhancement of these small lesions and no other contrast enhancing lesions are identified. No other abnormal foci of increased or decreased signal intensity are seen anywhere intracranially. Normal gray/white matter differentiation.
Impression:
1. Two tiny white matter lesions adjacent to the trigone of the right lateral ventricle without evidence of surrounding edema or mass effect and not demonstrating contrast enhancement. The largest of these measures about 4 mm in size and the second measures 2 mm. These lesions are nonspecific and could represent some chronis gliosis or scarring. Early demyelinating disease cannot be entirely excluded.
2. Otherwise normal appearing magnetic resonance imaging study of the brain.
Any ideas? Thank you!
Terrified. Been diagnosed with "possible MS" for 8 years. Since they threw the word "possible" in there and then said "but try Avonex", at that time I elected not to use Avonex for something I only possibly might have. It seemed too strong of a solution for a problem they weren't sure about.
Well, they're sure now. More and bigger lesions. Worsened symptoms Now, instead of Avonex, it's Refib. I got the Refib suitcase info pack from my doctor. That is daunting in and of itself.
I'm just scared. Scared and very, very exhausted. I'm also mad as hell, too. I am so afraid this will keep me from the things I love the most. I'm physically fit and enjoy horses and exercising. As of late, I can barely ride for 30 minutes without getting tired - I know my horse must be grateful because he gets groomed for doing little work.
Just scared. I'm new to this. I have no flippin idea what to expect and until my insurance pre-cert comes back, I don't even know if I can afford this Refib. There is absolutely no cost information that I can find online about this drug. What gives????
I don't guess I have questions. I just feel very much in shock and when I'm not in shock I'm either grieving or pissed off. I also have lupus and antiphospholipid syndrome so don't have "just" ms, as if that wouldn't be enough by itself, huh??? See? I'm pissed. How do you quit being pissed off?
Well, they're sure now. More and bigger lesions. Worsened symptoms Now, instead of Avonex, it's Refib. I got the Refib suitcase info pack from my doctor. That is daunting in and of itself.
I'm just scared. Scared and very, very exhausted. I'm also mad as hell, too. I am so afraid this will keep me from the things I love the most. I'm physically fit and enjoy horses and exercising. As of late, I can barely ride for 30 minutes without getting tired - I know my horse must be grateful because he gets groomed for doing little work.
Just scared. I'm new to this. I have no flippin idea what to expect and until my insurance pre-cert comes back, I don't even know if I can afford this Refib. There is absolutely no cost information that I can find online about this drug. What gives????
I don't guess I have questions. I just feel very much in shock and when I'm not in shock I'm either grieving or pissed off. I also have lupus and antiphospholipid syndrome so don't have "just" ms, as if that wouldn't be enough by itself, huh??? See? I'm pissed. How do you quit being pissed off?
I have been told that it is ok and acceptible to have up to so many hyperintensities for your age. They are common in migraines & I have several of these and do not consider them among my top worries. I have experienced many different migraine sx over the years of my life, and they also include a teary red eye. My mother had a migraine which caused one eye to swell and shut --it seemed like a migraine to her, and then, like most things, it went away.
Migraines are really impacting on one's life, that is a big problem with them, and like other problems, it matters how frequently, how bad and what the associated symptoms are--different for each person, just as MS or Lyme, where not every case is debilitating, and medications can really help. It might be helpful to remember that people don't usually die from these problems, but there are plenty of awful things out there that take out a beautiful life without much warning, from illness to car accident.
One more thing on the migraine: I wonder if maybe the reason for the hyper intensities is micro-strokes from a patent foramen ovale (PFO). This is a "hole in the heart" that we all have at birth, and it closes in most people, but about 1 in 4 of us it doesn't close, and its been in the news that 65% of migraineurs have the hole, and postulated that tiny emboli are formed and cause some blockages up in the brain. Plus, migraineurs are more likely to have strokes. Interesting...what does it mean for what to do? I can think it means do your best at modifying behavior to cut down all stroke risk factors possible--good weight, avoid hypertension, good diet, good exercise, & avoid migraine triggers--here's a thought: maybe its changes in the heart rhythms that certain triggers cause and then the migraine follows. I have also wondered about daily aspirin as a help, and fish oil plus calcium for good blood vessels.
Migraines are really impacting on one's life, that is a big problem with them, and like other problems, it matters how frequently, how bad and what the associated symptoms are--different for each person, just as MS or Lyme, where not every case is debilitating, and medications can really help. It might be helpful to remember that people don't usually die from these problems, but there are plenty of awful things out there that take out a beautiful life without much warning, from illness to car accident.
One more thing on the migraine: I wonder if maybe the reason for the hyper intensities is micro-strokes from a patent foramen ovale (PFO). This is a "hole in the heart" that we all have at birth, and it closes in most people, but about 1 in 4 of us it doesn't close, and its been in the news that 65% of migraineurs have the hole, and postulated that tiny emboli are formed and cause some blockages up in the brain. Plus, migraineurs are more likely to have strokes. Interesting...what does it mean for what to do? I can think it means do your best at modifying behavior to cut down all stroke risk factors possible--good weight, avoid hypertension, good diet, good exercise, & avoid migraine triggers--here's a thought: maybe its changes in the heart rhythms that certain triggers cause and then the migraine follows. I have also wondered about daily aspirin as a help, and fish oil plus calcium for good blood vessels.
I have been told that it is ok and acceptible to have up to so many hyperintensities for your age. They are common in migraines & I have several of these and do not consider them among my top worries. I have experienced many different migraine sx over the years of my life, and they also include a teary red eye. My mother had a migraine which caused one eye to swell and shut --it seemed like a migraine to her, and then, like most things, it went away.
Migraines are really impacting on one's life, that is a big problem with them, and like other problems, it matters how frequently, how bad and what the associated symptoms are--different for each person, just as MS or Lyme, where not every case is debilitating, and medications can really help. It might be helpful to remember that people don't usually die from these problems, but there are plenty of awful things out there that take out a beautiful life without much warning, from illness to car accident.
One more thing on the migraine: I wonder if maybe the reason for the hyper intensities is micro-strokes from a patent foramen ovale (PFO). This is a "hole in the heart" that we all have at birth, and it closes in most people, but about 1 in 4 of us it doesn't close, and its been in the news that 65% of migraineurs have the hole, and postulated that tiny emboli are formed and cause some blockages up in the brain. Plus, migraineurs are more likely to have strokes. Interesting...what does it mean for what to do? I can think it means do your best at modifying behavior to cut down all stroke risk factors possible--good weight, avoid hypertension, good diet, good exercise, & avoid migraine triggers--here's a thought: maybe its changes in the heart rhythms that certain triggers cause and then the migraine follows. I have also wondered about daily aspirin as a help, and fish oil plus calcium for good blood vessels.
Migraines are really impacting on one's life, that is a big problem with them, and like other problems, it matters how frequently, how bad and what the associated symptoms are--different for each person, just as MS or Lyme, where not every case is debilitating, and medications can really help. It might be helpful to remember that people don't usually die from these problems, but there are plenty of awful things out there that take out a beautiful life without much warning, from illness to car accident.
One more thing on the migraine: I wonder if maybe the reason for the hyper intensities is micro-strokes from a patent foramen ovale (PFO). This is a "hole in the heart" that we all have at birth, and it closes in most people, but about 1 in 4 of us it doesn't close, and its been in the news that 65% of migraineurs have the hole, and postulated that tiny emboli are formed and cause some blockages up in the brain. Plus, migraineurs are more likely to have strokes. Interesting...what does it mean for what to do? I can think it means do your best at modifying behavior to cut down all stroke risk factors possible--good weight, avoid hypertension, good diet, good exercise, & avoid migraine triggers--here's a thought: maybe its changes in the heart rhythms that certain triggers cause and then the migraine follows. I have also wondered about daily aspirin as a help, and fish oil plus calcium for good blood vessels.
You might want to read up on migraine headaches in light of your symptoms.
The right sided facial paralysis is called Bell's Palsy. That was the first symptom i had when I got diagnosed with lyme disease. 1 month doxycylcine and my face eventually went back to normal.
I am a 28 year old female. I woke up a week ago to right side facial numbness, including tongue & teeth. I have been to the doctor & had a Cat Scan & MRI. MRI shows 2 white matter lesions, but no other symptoms of MS & top spinal cord looked clear. A week before this started, I woke up in the middle of the night with a horrific headache & was seeing white halos around everything. Day before the numbness, I also had a sever headache, though it went away in a few hours. I have also had an extreme amount of anxiety leading up to this for about a year. Can anyone shed some light on this? I am ready to have a nervous breakdown!
I also have been going thru many test to sort out what may be going on with my pain in back, right leg, neck and headaches that come with double vison and dizzieness. My neuro Doctor has sent me for MRI"S MRA"S and clearly it shows lesions as big as 6mm at the centrum semiovale and corona radiata bilaterlly. no one wants to give me any straight answers! Instead I have been sent to Doctor to Doctor with many test inbetween, including a meilagram which put me in more pain then I was before the test. I have also seen a MS Doctor at Strong Hospital, which they are not ruling out MS but I have none of the normal systoms that come with MS.. HELP please.. where do I go from here..
Thanks all
Thanks all
First of all, keep in mind that I am unable to diagnose you because I am unable to examine you, this forum is for educational purposes.
The small white matter lesions are frequently encountered in the MRIs of patients with headaches (especially migraines). There are other things that can also cause these lesions such as high blood pressure, traumatic brain injury, migraines, and old strokes. Each of the diseases tends to have different distributions of the lesions, but no pattern of white matter lesions is completely specific for any one disorder. The symptoms and story that you describe are most consistent with classic migraine or migraine with aura (these headaches can be associated with focal neurologic features-such as the arm tingling, and also can cause a confused/foggy state). The red teary may not be related, but there are also headaches with autonomic features that can also cause these symptoms. One caution is that a common drug used for headaches (topamax) has been associated with glaucoma (rarely) which presents with a red, painful eye that is unable to see. I would suggest that you start a headache prevenative medication such as elavil, nadolol, verapamil, topamax, etc (taken daily). I am not apposed to further testing and the referal to the MS center. Since there is not positive confirmatory test that can tell you that the spots are due to migraines, testing for MS in a extensive fashion is usually the best thing to due (to rule MS out).
I hope this has been helpful.
The small white matter lesions are frequently encountered in the MRIs of patients with headaches (especially migraines). There are other things that can also cause these lesions such as high blood pressure, traumatic brain injury, migraines, and old strokes. Each of the diseases tends to have different distributions of the lesions, but no pattern of white matter lesions is completely specific for any one disorder. The symptoms and story that you describe are most consistent with classic migraine or migraine with aura (these headaches can be associated with focal neurologic features-such as the arm tingling, and also can cause a confused/foggy state). The red teary may not be related, but there are also headaches with autonomic features that can also cause these symptoms. One caution is that a common drug used for headaches (topamax) has been associated with glaucoma (rarely) which presents with a red, painful eye that is unable to see. I would suggest that you start a headache prevenative medication such as elavil, nadolol, verapamil, topamax, etc (taken daily). I am not apposed to further testing and the referal to the MS center. Since there is not positive confirmatory test that can tell you that the spots are due to migraines, testing for MS in a extensive fashion is usually the best thing to due (to rule MS out).
I hope this has been helpful.
28/M/White
BRAIN WITH & W/O CONTRAST
2/15/06
INDICATION:
Evaluate for MS. Parethesias, weakness, and visual changes.
TECHNIQUE:
Multiplanar T1, T2 weighted and FLAIR sequences were obtained prior to intravenous contrast. After intravenous Omniscan, T1 images were obtained.
FINDINGS:
There is no MRI evidence of midline shift or mass effect. Multiple round to ovoid foci of increased T2 weighted signal are noted in the periventricular and deep white matter of both cerebral hemispheres. Some foci within the centrum semi-ovale are oriented perpendicular to the plane of the corpus callosum and cingulate gyrus, suspicious for MS plaques. More ill-defined increased T2 weighted signal is noted in the periventricular white matter. Faint nodular areas of increased T2 weighted signal are noted within the corpus callosum. A small, 3-4 mm ovoid focus of increased T2 weighted signal is seen within the posterior aspect of the left middle cerebellar peduncle.
After IV contrast, at least five of the presumed plaques appear to enhance, the largest seen in the right frontal white matter, measuring 8 mm in maximum AP dimension.
Normal signal void is demonstrated in the major vasculature at the base of the brain. Visualized paranasal sinuses appear clear.
IMPRESSION:
Multiple round to ovoid foci of increased T2 weighted signal in the periventricular and deep white matter of both cerebral hemispheres, as well as within the left middle cerebellar peduncle and corpus callosum. Several lesions appear to enhance after IV contrast. Findings are non-specific, but are suspicious for MS plaques. Other etiologies, such as Vasculitis or Lyme disease, could produce similar findings. Clinical correlation advised.
--
CERVICAL SPINE WITH & W/O GADOLINIUM
4/05/06
HISTORY:
Chronic posterior neck pain and stiffness w/ hand parethesias.
TECHNIQUE:
Multiplanar T1 and T2 weighted sequences were obtained before and after intravenous gadolinium administration.
FINDINGS:
The bone marrow signal appears well maintained. There is reversal of normal cervical lordosis. Disc space heights appear well maintained. Not acute verterbral body compression fracture is demonstrated. The carniocervical junction appears unremarkable.
Saggital STIR sequence shows extensive signal abnormality within the cervical spinal cord, throughout the entire cervical spine. No cord compression is demonstrated. The neural canal regions appear ample in size.
Gladolinium-enhanced imaging shows no abnormal enhancement.
IMPRESSION:
Extensive areas of hyperintense signal abnormality within the cervical spinal cord, most consistent with a demyelinating process. No enhancement was demonstrated. Please see report from MRI of the brain.
BRAIN WITH & W/O CONTRAST
2/15/06
INDICATION:
Evaluate for MS. Parethesias, weakness, and visual changes.
TECHNIQUE:
Multiplanar T1, T2 weighted and FLAIR sequences were obtained prior to intravenous contrast. After intravenous Omniscan, T1 images were obtained.
FINDINGS:
There is no MRI evidence of midline shift or mass effect. Multiple round to ovoid foci of increased T2 weighted signal are noted in the periventricular and deep white matter of both cerebral hemispheres. Some foci within the centrum semi-ovale are oriented perpendicular to the plane of the corpus callosum and cingulate gyrus, suspicious for MS plaques. More ill-defined increased T2 weighted signal is noted in the periventricular white matter. Faint nodular areas of increased T2 weighted signal are noted within the corpus callosum. A small, 3-4 mm ovoid focus of increased T2 weighted signal is seen within the posterior aspect of the left middle cerebellar peduncle.
After IV contrast, at least five of the presumed plaques appear to enhance, the largest seen in the right frontal white matter, measuring 8 mm in maximum AP dimension.
Normal signal void is demonstrated in the major vasculature at the base of the brain. Visualized paranasal sinuses appear clear.
IMPRESSION:
Multiple round to ovoid foci of increased T2 weighted signal in the periventricular and deep white matter of both cerebral hemispheres, as well as within the left middle cerebellar peduncle and corpus callosum. Several lesions appear to enhance after IV contrast. Findings are non-specific, but are suspicious for MS plaques. Other etiologies, such as Vasculitis or Lyme disease, could produce similar findings. Clinical correlation advised.
--
CERVICAL SPINE WITH & W/O GADOLINIUM
4/05/06
HISTORY:
Chronic posterior neck pain and stiffness w/ hand parethesias.
TECHNIQUE:
Multiplanar T1 and T2 weighted sequences were obtained before and after intravenous gadolinium administration.
FINDINGS:
The bone marrow signal appears well maintained. There is reversal of normal cervical lordosis. Disc space heights appear well maintained. Not acute verterbral body compression fracture is demonstrated. The carniocervical junction appears unremarkable.
Saggital STIR sequence shows extensive signal abnormality within the cervical spinal cord, throughout the entire cervical spine. No cord compression is demonstrated. The neural canal regions appear ample in size.
Gladolinium-enhanced imaging shows no abnormal enhancement.
IMPRESSION:
Extensive areas of hyperintense signal abnormality within the cervical spinal cord, most consistent with a demyelinating process. No enhancement was demonstrated. Please see report from MRI of the brain.
Well, how long ago was this? And, I read this-I cannot account for bad reporting. However, I personally know a man "Paul" who was on Montel's show, who was not speaking, and he is on LDN and is, according to himself, asymptomatic.
I vibrate internally and have paresthesias of the hands-SO-I know what it is like to have my symptoms unnoticed. I also was in a wheelchair.
I am fine now and have been for a long long time.
I vibrate internally and have paresthesias of the hands-SO-I know what it is like to have my symptoms unnoticed. I also was in a wheelchair.
I am fine now and have been for a long long time.
"Check out LDN and Montel Williams..he is basically asymptomatic, and many many more. "
In your dreams. Montel talked about going from power squatting huge amounts of weight during military training to having pain while doing so. Shin and leg pain. Pain which kept growing. Finally it got so bad, he accidentally burned his legs severely because he could not tell the pain from a nearby heater which scared his legs. He went to a lot of doctors for almost two decades, I think he said, with symptoms. He now says even percocet does not kill the pain of his MS and he uses marijuana for pain control.
I would hardly call him asymptomatic, he's suffered a great deal. Just because he is a very driven personality who happens to have a regular TV show by his natural nature of being an alpha type personality it does not mean he is asymptomatic. A lot of us have symptoms and standing next to me you might think not a thing is wrong with me.
JFK had a lot of symptoms, too, and hid them very very well. Different disease, similar strategy.
In your dreams. Montel talked about going from power squatting huge amounts of weight during military training to having pain while doing so. Shin and leg pain. Pain which kept growing. Finally it got so bad, he accidentally burned his legs severely because he could not tell the pain from a nearby heater which scared his legs. He went to a lot of doctors for almost two decades, I think he said, with symptoms. He now says even percocet does not kill the pain of his MS and he uses marijuana for pain control.
I would hardly call him asymptomatic, he's suffered a great deal. Just because he is a very driven personality who happens to have a regular TV show by his natural nature of being an alpha type personality it does not mean he is asymptomatic. A lot of us have symptoms and standing next to me you might think not a thing is wrong with me.
JFK had a lot of symptoms, too, and hid them very very well. Different disease, similar strategy.
Ok...
Now, go back, and read what I wrote.
First and foremost-I am sorry that you have MS. I went thru the terror of it myself. We have differing views.
Point in fact: most people do not know that they have Lyme when it is acute and therefore it progresses to "Late Stage." Thus-MS (which as you know is a variable term in concrete medicine).
Point in fact: More and more studies are showing that MS is enviro and that supressing the immune system is stupid in its case. Check out LDN and Montel Williams..he is basically asymptomatic, and many many more.
Point in fact: A Lyme diagnosis is almost never concrete. So, I could have true MS, if, there is such a thing.
Please, do not, be hurt by my opinion. It is not to discredit people, and, I am not telling TESSARIO to ignore the lesions. I am telling him not to have a nervous breakdown.
MSers, as you say, as well as Lymies, as we say, do have a tendency to marry the dx. This is not mentally healthy-at all.
We must all fight together. We must have our own opinions. We must make educated guesses.
Please, don't we this way. You and I both are waiting on a powderkeg for cures.
Peace.
John.
Now, go back, and read what I wrote.
First and foremost-I am sorry that you have MS. I went thru the terror of it myself. We have differing views.
Point in fact: most people do not know that they have Lyme when it is acute and therefore it progresses to "Late Stage." Thus-MS (which as you know is a variable term in concrete medicine).
Point in fact: More and more studies are showing that MS is enviro and that supressing the immune system is stupid in its case. Check out LDN and Montel Williams..he is basically asymptomatic, and many many more.
Point in fact: A Lyme diagnosis is almost never concrete. So, I could have true MS, if, there is such a thing.
Please, do not, be hurt by my opinion. It is not to discredit people, and, I am not telling TESSARIO to ignore the lesions. I am telling him not to have a nervous breakdown.
MSers, as you say, as well as Lymies, as we say, do have a tendency to marry the dx. This is not mentally healthy-at all.
We must all fight together. We must have our own opinions. We must make educated guesses.
Please, don't we this way. You and I both are waiting on a powderkeg for cures.
Peace.
John.
While I do agree the lesions can be caused by any number of disorders, I will strongly disagree with the statement made by JCmcc that 'Lyme is MS'. If diagnosed in the early stages, Lyme CAN be cured with antibiotics. MS cannot. No matter if it's found in an early stage or late stage. And I find the casual connection of the two disorders extremely disheartening. MS is, at best, manageable.
I will also agree that Lyme is becoming more commonplace even though it is STILL difficult to diagnose and I agree that it should never be overlooked as a possibility when looking for a name to be attached to a condition. I will even agree that if left untreated, Lyme can advance and become devastating to your body. But if precautions are taken before and after possible exposure, Lyme may be avoided all together.
I wish I could say the same thing about MS. If there was something that I could have avoided to prevent my MS, I would have. But we (MSers) do whatever we can to lead as normal a life as possible. It is NOT a death sentence.
All that being said Tsarrio, the lesions should not be swept aside. And there is a reason for the symptoms you are having. Despite the frustration I am sure you will suffer before that reason is found, don't give up looking for the answers you need. Regardless of the diagnosis, once it is made, it is a relief. Only then can the treatments you need to cure/manage/cope begin. Good Luck finding the answers you are looking for!!
I will also agree that Lyme is becoming more commonplace even though it is STILL difficult to diagnose and I agree that it should never be overlooked as a possibility when looking for a name to be attached to a condition. I will even agree that if left untreated, Lyme can advance and become devastating to your body. But if precautions are taken before and after possible exposure, Lyme may be avoided all together.
I wish I could say the same thing about MS. If there was something that I could have avoided to prevent my MS, I would have. But we (MSers) do whatever we can to lead as normal a life as possible. It is NOT a death sentence.
All that being said Tsarrio, the lesions should not be swept aside. And there is a reason for the symptoms you are having. Despite the frustration I am sure you will suffer before that reason is found, don't give up looking for the answers you need. Regardless of the diagnosis, once it is made, it is a relief. Only then can the treatments you need to cure/manage/cope begin. Good Luck finding the answers you are looking for!!
I'm betting it turns out you have migraines, which can cause those types of lesions. For the radiologist to say he/she can't exclude MS is not the same as saying you have MS (they just try to cover their tracks). Years ago I went through a huge amount of anxiety when a few small lesions showed up on my MRI after I had a variety of odd symptoms, including my right leg tingling (and the radiologist kind of gave an ambiguous reading); I went to two famous neurologists for clarification, and they both said the spots were likely from migraines. And years later, I still definitely do not have MS (but I do have complex migraines). So keep your appointment, but in the meantime, don't be too worried. By the way, the arm tingling could be due to some kind of peripheral neuropathy or nerve compression; the best thing to take for neuropathy is 600 mg. of alpha lipoic acid daily (in divided doses). You can buy it at vitamin stores like GNC. You can google alpha lipoic acid for more information. God bless.
You didn't ask me, but here is what I know.
If the lesions have anything to do with the headaches, then, the headache is the cause of the lesion or the lesion is caused by a condition where a symptom is headache. Hard to tell.
I have read many studies that say that so-called MS lesions are found in ats of many dead patients who never had symptoms or a disease of the CNS. Lesions are always torally non-specific. For example; what I have learned in MS is that though they are suspicious for MS plaques, space and time, is a really big deal. They watch how they progress, what they do-and not uncommonly MS diagnoses are removed. This has happened more than a few times per MS specialist.
Hope I helped.
If the lesions have anything to do with the headaches, then, the headache is the cause of the lesion or the lesion is caused by a condition where a symptom is headache. Hard to tell.
I have read many studies that say that so-called MS lesions are found in ats of many dead patients who never had symptoms or a disease of the CNS. Lesions are always torally non-specific. For example; what I have learned in MS is that though they are suspicious for MS plaques, space and time, is a really big deal. They watch how they progress, what they do-and not uncommonly MS diagnoses are removed. This has happened more than a few times per MS specialist.
Hope I helped.
Migraine headaches can also cause lesions to appear on the MRI. Your neurologist should know this.
I am not a doctor and so, for what it is worth:
One thing that I have learned with diagnoses and illness is that pathology/pathogenesis is most important. Know your past, know the present and keep track of it. Such pathology and doctor/patient communication leads to a thorough diagnosis.
I think that jumping to MS is a bit out of bounds here. These lesions are non-specific and could be caused by a number of variables. These variables can also cause the same symptoms that you describe.
There is, of course, the infamous and unpopular Lyme disease. There is Vasculitis, Syphilis -all of which are commonly undetected. It would be worthwhile to look into other options.
I am 28/M. I had many lesions on both sides of the brain and in the c-spine. All round and ovoid and some which enhanced. Doc said, "YOU HAVE MS!" Well--after a nervous breakdown, and a ton of my own research-I found that I in fact had LYME DISEASE. But, in my opinion, much to be argued I am sure-Lyme is MS. So, I am now, after losing my ability to walk and over 83 symptoms ASYMPTOMATIC.
You may want to do a couple of things: 1. Google "LDN" or "Low Dose Naltrexone."
2. Go to www.lymenet.org and do some research.
3. Do not marry a diagnosis and do not let it own or consume you.
4. Remember that you are in charge and that doctors are here to help you-they do not seal the case.
5. Stand up for yourself and learn everything you can until a true diagnoses is confirmed and substantiated.
One thing that I have learned with diagnoses and illness is that pathology/pathogenesis is most important. Know your past, know the present and keep track of it. Such pathology and doctor/patient communication leads to a thorough diagnosis.
I think that jumping to MS is a bit out of bounds here. These lesions are non-specific and could be caused by a number of variables. These variables can also cause the same symptoms that you describe.
There is, of course, the infamous and unpopular Lyme disease. There is Vasculitis, Syphilis -all of which are commonly undetected. It would be worthwhile to look into other options.
I am 28/M. I had many lesions on both sides of the brain and in the c-spine. All round and ovoid and some which enhanced. Doc said, "YOU HAVE MS!" Well--after a nervous breakdown, and a ton of my own research-I found that I in fact had LYME DISEASE. But, in my opinion, much to be argued I am sure-Lyme is MS. So, I am now, after losing my ability to walk and over 83 symptoms ASYMPTOMATIC.
You may want to do a couple of things: 1. Google "LDN" or "Low Dose Naltrexone."
2. Go to www.lymenet.org and do some research.
3. Do not marry a diagnosis and do not let it own or consume you.
4. Remember that you are in charge and that doctors are here to help you-they do not seal the case.
5. Stand up for yourself and learn everything you can until a true diagnoses is confirmed and substantiated.
PS,
I want to make it clear that I walk now. I am as I was before with only 1 slightly annoying symptom (internal vibrating). I was numb, I was tired, I wasn't walking, I was dizzy, I was burry, malaise was my life. I had myclonus and clonus general---to name a few!
A positive outlook and being very strong and fighting for myself too helped in my healing.
You can e-mail me anytime if you want to talk about this stuff. I can tell you about my pathology system (63 pages) and how Yale upheld my self made diagnosis. It may help you out.
My peace.
I want to make it clear that I walk now. I am as I was before with only 1 slightly annoying symptom (internal vibrating). I was numb, I was tired, I wasn't walking, I was dizzy, I was burry, malaise was my life. I had myclonus and clonus general---to name a few!
A positive outlook and being very strong and fighting for myself too helped in my healing.
You can e-mail me anytime if you want to talk about this stuff. I can tell you about my pathology system (63 pages) and how Yale upheld my self made diagnosis. It may help you out.
My peace.
I forgot to mention, I have also done L-spine and C-spine MRIs w/out contrast - both are negative. My current neuro thinks I have complex migraines, but now that he saw the MRI result with 2 lesions, he is referring me to the MS clinic.
I have similar symptoms, left sided tingling and numbness, have been through all sorts of testing, and still don'y know what is causing it.
In Oct. MRI showed 1 lesion.......Had follow-up MRI in Jan., it showed a total of 5 hyperintense lesions, (that was almost 3 months ago, for all I know there could be more by now)
I also have severe headaches, but what I would like to know is.......Does the headache cause the lesions or do the lesions cause the headache????????
All my other tests were basically normal, initially Neuro was thinking MS, now he says he doesn't know what it is, I have been tested for basically everything, and nothing has really shown up. Possibly Microangiopathy?
Bottom line: Try not to get all worked up over the MRI results......when I first heard that I had lesions, I almost wigged!
But after reading online, especially here, I've learned that it's not that uncommon.....apparently there are lots of us with lesions on the brain..
I'm not saying it's normal, just that there seems to be a lot of people in the same boat.......similar non-specific symptoms, with no definite diagnosis.
Hang in there!
In Oct. MRI showed 1 lesion.......Had follow-up MRI in Jan., it showed a total of 5 hyperintense lesions, (that was almost 3 months ago, for all I know there could be more by now)
I also have severe headaches, but what I would like to know is.......Does the headache cause the lesions or do the lesions cause the headache????????
All my other tests were basically normal, initially Neuro was thinking MS, now he says he doesn't know what it is, I have been tested for basically everything, and nothing has really shown up. Possibly Microangiopathy?
Bottom line: Try not to get all worked up over the MRI results......when I first heard that I had lesions, I almost wigged!
But after reading online, especially here, I've learned that it's not that uncommon.....apparently there are lots of us with lesions on the brain..
I'm not saying it's normal, just that there seems to be a lot of people in the same boat.......similar non-specific symptoms, with no definite diagnosis.
Hang in there!
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