I was 10 Years old in 1973. A classmate died of meningitis over Thanksgiving weekend. Nobody else got it. But I'm super freaked to day about how he disappeared so quickly and freaked out all us kids. Thanks for your presentation.
I had viral spinal meningitis when I was 7 none of my family paid attention to me for weeks it took my soccer coach to see how bad I was. I would run for the ball and fall,run for the ball and fall. no one can imagine the pain from how bad the headache was. that night I put my head trough 6 panes of glass to try and take the pain away. at the hospital they didn't have any time to numb me for the spinal tap . shortly after I was moved to a room that anyone coming in had to be in full bio suites it tried to kill me twice I spent 6 months in there and another year in doors after that. the lasting effects now at 36 are long yet still no one listens when your 36 so if people think viral cant be just a bad I can tell you that it can be. don't waste time to get to the hospital.
Josh Cook ooo,sorry that happened. But i believe you to the fullest. It is a tough bad memory,but is good to understand the joy and peace of not having pain. I was 54 thru chemo of 27, 4hr and 5 minute session of all 3 chemo poisons. Felt my brain burning on fire where my spine top ended. A lit fire under my brain. Nobody believed me,not even the nurse. It was torture. God brings us home in His time,when He is ready. The pain could have killed us,but we were spared. I always wonder if i aquired any of these during chemo because the oncologist would never make a single remark about it. Live long and peace and joy to you and yours.
That scares me Josh. I find it tragic how people are so quick to disbelieve pain they can’t see. It sounds crazy to put your head through glass to try to ease pain to those who haven’t experienced it, I get it, and can only thank all that is good that you finally got to the hospital.
I had viral meningitis which was horrible... returning to college I WAS NOT the same person. I could not retain any new information. I was great at public speak, not after being ill. After being ill I was far from the smart confident person I was. Til this day I get really bad migraine headache that are so bad that I can’t SEE and vomit the pain is so excruciating. Life after meningitis is anything but normal.
Thank you for saying this. NONE of my doctors ever told me I would not be the same after the viral infection was under control. But I find it hard to think, talk and remember. I struggle with handling my own finances, paperwork and medication management. I used to be fairly intelligent. Now, I am just not the same.
I had this last year. It came on so fast that I didn’t get the chance to recognise how ill I was. Brain cognition was lost and my hearing and sight so affected that I couldn’t text or phone to ask for help even if I had the thought to. I literally couldn’t move. I remember being aware my leg was in an unnatural position, but I was unable to move, my muscles had given up and my body was a dead weight. It was absolutely dreadful and took me a good while to recover speech, movement and brain function. Interestingly, during that recovery period it drastically slowed down my ADHD brain and I got a glimpse at the world around me in, I suppose, real time. It allowed me to make some important decisions before the mania set back in. I’m glad I got to experience that at least. I was lucky that my mother turned up after a 4 hour train journey because she hadn’t heard from me. She called an ambulance, twice. The first time meningitis was discounted because I wasn’t actually vomiting. The second time, I was wheel-chaired into to the ER, but received nothing but IV pain meds and hydration and then the doctor sent me home alone in a taxi ..despite the pain and the fact that I couldn’t walk, I could barely talk - very slow and confused, I couldn’t move without major disorientation, the light, the sound and and ..they packaged me off stating it was probably the flu. I wasn’t able to explain otherwise and well, there we are. My doctor wouldn’t then believe me because I’d received no diagnosis from the hospital. It was day 5 of my being ill that I got to the hospital, so the doctor there, I’m in no doubt, figured it wasn’t bacterial, so even if it was VM there was nothing there to be done, but rest and pain meds at home. I’m not sure my brain is quite as sharp as it was before it felt like it wanted to explode, with severe burning at the base of my skull/neck, but I am here, alive and kicking and for that I am truly grateful.
4:26 Thank you for saying this!!! My viral meningitis went undiagnosed and untreated for 6 weeks in spite of going to ER twice. My brain hasn't been the same since. Also I get super exhausted super fast. In three months it will be a year since infection. No medical professional ever told me there might be long term effects. But I am learning there are only because I am seeking information and answers and connecting with other post Meningitis patients who are experiencing the same things I am.
“No, it can’t be from the meningitis, the basic tests say you’re okay so you’re probably making it up to try get strong painkillers, but if you aren’t then have you tried talking to someone? It’s probably all in your head and I’m sure talking therapy would help, there’s really nothing *that* wrong with you.” This is what I’ve had various doctors tell me and I’ve been on morphine for constant headaches for a decade now because the meningitis headache as a child only eased up, it never went away. Some days it’s tolerable, other days all I can think about is how I want to end everything because I can’t take the suffering any more. And my doctor who agreed with the morphine treatment for the past few years has now changed her tune and decided I need to stop the morphine and start seeing a counsellor since everyone knows talking about pain MAGICALLY makes it go away! 🙄 Trying to get people to believe me is the hardest part because they’ve NEVER been in that much pain for such a long time before and they simply can’t imagine what it’s like, and I’m sure it must be the same for you too. Most days I just want to give up for good. I can only take so much more before it all becomes too much. I never asked for any this, and nobody even cares.
@nightblade628 I care and I totally understand. I'm so sorry you are experiencing this level of pain and doctor denial. I have been disabled from Fibromyalgia for 34 years, so I get it. When I got Covid, then Long Covid, then Viral Meningitis, then Encephalopathy then Covid AGAIN -- ALL within the last three years, that really has led to horrendous pain. But also brain fog, aphasia, abnormal weight gain, light sensitivity, stimulus overload, blah, blah, blah, on and on. Keep on pursuing answers. You know already what they are likely to say. I understand that too. It sucks!! You be your own best advocate. I know it's super hard but write it all out little by little as you can tolerate. Best wishes to you. Never give up.
Great video. Thank you for the information. I am glad to hear you do the lumbar puncture test because you realize how bad it can get/ rule out bacterial meningitis. Most doctors will probably write it off as a migraine or the flu.
I had viral meningitis with severe encephalitis after having COVID19. At the hospital they did a CT scan, blood tests + lumbar puncture, I was hospitalized for 10 days to receive treatment. But you forgot to mention, the lumbar puncture usually causes more headaches until the body recovers the fluid that was taken out during the LP.
I think I have viral meningitis. I have severe headache and stiff neck for 3 days now. I am just realizing it may be meningitis. I had Covid 3 weeks ago. Thanks for sharing your experience.
In my case, I got meningitis a year after Covid and Long Covid. How far apart were your two diagnoses? Opposite from your experience, my headache was relieved by the reduction of CSF vis lumbar puncture. Less pressure on my brain. I got teary with relief! Meningitis pain is no joke.
This video was so helpful. Thank you for sharing and explaining viral meningitis. I think I may have this because I have a stiff neck and worst headache ever. I will see the doctor tomorrow.
The human body should not be taken for granted or disrespected. Many don't listen or notice their symptoms pay attention to how you feel write down at what time it repeats. pain scale 1-10 .
I had viral meningitis 3 times in my life. 1st time I went to the ER.. they did a spinal tap. Told me I had the viral M. They sent me home with pain killers I recovered. The other 2 times I took pain meds until it cleared. Viral Meningitis can turn into Encephalitis which can be deadly..
In this series of educational videos I think it would be beneficial to show a spinal tap being performed. My reasoning behind this is that I feel some people may not be seeking treatment for their symptoms is fear of having this specific procedure performed. Please take this into consideration.
I was scared to have the lumbar puncture but was in so much pain and had been for so long (6 weeks undiagnosed in spite of 2 ER visits) that I was willing for anything. It was actually a blesséd relief to have some of that pressure removed from my brain via the lumbar puncture. They were very careful of my aftercare after the lumbar puncture - made sure I didn't move a muscle for two hours afterwards - so I had no bad side effects from it. They were great. Super grateful for those hospital staff that worked with me. ❤
When I got meningitis my mind went from being very easy to remember short term memory things for test and I coukd retain and learn so easy but after I noticed I couldn't think howbi used to and wasn't as smart and when I trained for 3 months to work for at&t as a technical support agent and when we tok the exam you had to pass to become an agent it took me almost the whole time alloted as there was so much to remember and I was the one still testing and I never had problems passing test like that and that's how I used to pass classes was be a good tester but to me forever to recall everything I learned the previous 3 months and took forever remembering everything I learned and the pressure of the time slot also made me lose my ability to recall what I learned and I needed time to remember everything I learned and was just imagining wrong things before I took the time to recall tge facts. I knew I had brain damage than as my short term memory wasb Shot as was my ability to rapidly learn what I was taught.
I have a question I had viral meningitis was in the hospital for a week on pain medications. I started sleepwalking and while I was in the middle of the sleepwalking my legs would give out and I would fall. And I also started which has lingered which has been year-and-a-half some days I cannot wake up and stay up the whole day I have to constantly sleep. I have seen to sleep specialist for and both of them tell me that that's not related however in Reading about viral meningitis and people's experience they have had the same problem. What would be your recommendation as my next step to try to find some help to be able to function properly awake because it's gotten to the point to where I can't even drive out of town because I'm afraid that I will crash. Any help you could give me would really be appreciated
ive been very tired i cant find anyone to help me or diagnnos me. ive hd it two times before. ive come down with it agian. i now have an antibiotic its also reccomended to take fish oil and ive noticed vit e helps alot. but we have no real doctors down here. im in central louisiana.
Can a spinal tap check for a meningitis that occurred weeks ago? I had one that I think was maybe due to antidepressant medications. Because I felt very very ill during the 1st 3 days of treatment then stopped, and I felt gradually better. But felt very tired and exhausted for about a week (I was like "what ever this is; it's as if I had a very very bad flu". And during that time I strangely felt like having warm baths (I was having them multiple times a day; I didn't know why, I just felt like it and went and took a bath after a bath, then go to bed and reeeeeeesssssttttt. It was awful. When I went to the psychiatrists they said it's normal to feel anxiety during the 1st days of using medications. But that wasn't any kinds of anxiety. I had photophobia, and sound phobia, I thought I was becoming autistic due to Prozac (I was searching for "Prozac induced autism", poor me, I felt like the SSRIs were irritating my CNS, as if someone was up there spraying fire at my brain) When the I stopped the medications and the pain resided, I was unable to read and comprehend a thing, my IQ dropped, I turned from a smart person to a dumb person. I lost the ability to understand human emotions, I started to develop actual depression (I had a moderate depressive episode), I felt utterly squished from the inside out. I went to the ER 2 times, and they said that I had nothing, they gave me lorazepam and propranolol for the "anxiety, agitation, and heart palpitations" I didn't take any of them. And just waited it out. Ever since I lost the ability to sense time, didn't feel like my self, had depression, lost ability to use logic. And felt pressure behind my forehead that consided with these symptoms even after the pain went away. I wanted to see a neurologist but they kept saying that I should see a psychiatrist instead.
You are a very sensitive person, your reaction to medication could be because of a very sensitive gut, which is usually caused by food intolerance. May be you are gluten and dairy intolerant ? You should find a good naturopathic doctor and do the food sensitivities and toxicity level.
I’ve had recurrent meningitis for over 30 years. It’s awful & there is no cure. Cannot count how many times I’ve had it. The after effects are horrible. It gets worse with each episode.
I hate this sickness so much I lost my very childhood best friend with this why the doctors didn’t know it was meningitis it was too late he was comatose then die in 5 days why they didn’t know until it’s late they said he was on drugs because he forgot things? I’m just so hurt it was too quick Doc .
I had been attacked by a cute meningitis from 22nd of the December 2019 and treatment to Dr.Rahul Prasad till now but I could not walk freely . Please let me know after how many days I will walk freely? My CT scan Report is normal.
Jennifer Ferguson hi, I've been in hospital and treated for viral meningitis twice and I've suffered migraines all my life. The main difference I can say with me was the fever I had a temperature of 40c to 42c at the recorded highest and I was delirious, I felt generally unwell and just wanted to be left alone I had the splitting headache dizzyness and photosensitivety and I was very very sensitive to any noise. With migraines I've learnt they are very person specific and if it's something you've never felt before or it's unusual for you normal pattern then seek help asap! X
I was 10 Years old in 1973. A classmate died of meningitis over Thanksgiving weekend. Nobody else got it. But I'm super freaked to day about how he disappeared so quickly and freaked out all us kids. Thanks for your presentation.
I had viral spinal meningitis when I was 7 none of my family paid attention to me for weeks it took my soccer coach to see how bad I was. I would run for the ball and fall,run for the ball and fall. no one can imagine the pain from how bad the headache was. that night I put my head trough 6 panes of glass to try and take the pain away. at the hospital they didn't have any time to numb me for the spinal tap . shortly after I was moved to a room that anyone coming in had to be in full bio suites it tried to kill me twice I spent 6 months in there and another year in doors after that. the lasting effects now at 36 are long yet still no one listens when your 36 so if people think viral cant be just a bad I can tell you
that it can be. don't waste time to get to the hospital.
Josh Cook ooo,sorry that happened. But i believe you to the fullest. It is a tough bad memory,but is good to understand the joy and peace of not having pain. I was 54 thru chemo of 27, 4hr and 5 minute session of all 3 chemo poisons. Felt my brain burning on fire where my spine top ended. A lit fire under my brain. Nobody believed me,not even the nurse. It was torture. God brings us home in His time,when He is ready. The pain could have killed us,but we were spared. I always wonder if i aquired any of these during chemo because the oncologist would never make a single remark about it. Live long and peace and joy to you and yours.
That scares me Josh. I find it tragic how people are so quick to disbelieve pain they can’t see. It sounds crazy to put your head through glass to try to ease pain to those who haven’t experienced it, I get it, and can only thank all that is good that you finally got to the hospital.
I can feel your pain my son got this last year when he was 7 too...how i wAs helpless when he yelled because of horrible day of life
I had viral meningitis which was horrible... returning to college I WAS NOT the same person. I could not retain any new information. I was great at public speak, not after being ill. After being ill I was far from the smart confident person I was. Til this day I get really bad migraine headache that are so bad that I can’t SEE and vomit the pain is so excruciating. Life after meningitis is anything but normal.
Thank you for saying this. NONE of my doctors ever told me I would not be the same after the viral infection was under control. But I find it hard to think, talk and remember. I struggle with handling my own finances, paperwork and medication management. I used to be fairly intelligent. Now, I am just not the same.
I had this last year. It came on so fast that I didn’t get the chance to recognise how ill I was. Brain cognition was lost and my hearing and sight so affected that I couldn’t text or phone to ask for help even if I had the thought to. I literally couldn’t move. I remember being aware my leg was in an unnatural position, but I was unable to move, my muscles had given up and my body was a dead weight. It was absolutely dreadful and took me a good while to recover speech, movement and brain function. Interestingly, during that recovery period it drastically slowed down my ADHD brain and I got a glimpse at the world around me in, I suppose, real time. It allowed me to make some important decisions before the mania set back in. I’m glad I got to experience that at least.
I was lucky that my mother turned up after a 4 hour train journey because she hadn’t heard from me. She called an ambulance, twice. The first time meningitis was discounted because I wasn’t actually vomiting. The second time, I was wheel-chaired into to the ER, but received nothing but IV pain meds and hydration and then the doctor sent me home alone in a taxi ..despite the pain and the fact that I couldn’t walk, I could barely talk - very slow and confused, I couldn’t move without major disorientation, the light, the sound and and ..they packaged me off stating it was probably the flu. I wasn’t able to explain otherwise and well, there we are. My doctor wouldn’t then believe me because I’d received no diagnosis from the hospital. It was day 5 of my being ill that I got to the hospital, so the doctor there, I’m in no doubt, figured it wasn’t bacterial, so even if it was VM there was nothing there to be done, but rest and pain meds at home. I’m not sure my brain is quite as sharp as it was before it felt like it wanted to explode, with severe burning at the base of my skull/neck, but I am here, alive and kicking and for that I am truly grateful.
Cheryl van Hauen wow good you survived thanks for sharing your story I know now how my best friend feel on that day but I lost him to meningitis
madel galve Oh darling, I’m so sorry for your loss. Blessings to you.
Are you from the US? From my own experience and hearing about others, it seems doctors aren't aware enough or taking it seriously enough.
I have had this it was a nightmare best wishes to anyone who has had it
4:26 Thank you for saying this!!!
My viral meningitis went undiagnosed and untreated for 6 weeks in spite of going to ER twice. My brain hasn't been the same since. Also I get super exhausted super fast. In three months it will be a year since infection. No medical professional ever told me there might be long term effects. But I am learning there are only because I am seeking information and answers and connecting with other post Meningitis patients who are experiencing the same things I am.
“No, it can’t be from the meningitis, the basic tests say you’re okay so you’re probably making it up to try get strong painkillers, but if you aren’t then have you tried talking to someone? It’s probably all in your head and I’m sure talking therapy would help, there’s really nothing *that* wrong with you.”
This is what I’ve had various doctors tell me and I’ve been on morphine for constant headaches for a decade now because the meningitis headache as a child only eased up, it never went away. Some days it’s tolerable, other days all I can think about is how I want to end everything because I can’t take the suffering any more.
And my doctor who agreed with the morphine treatment for the past few years has now changed her tune and decided I need to stop the morphine and start seeing a counsellor since everyone knows talking about pain MAGICALLY makes it go away! 🙄
Trying to get people to believe me is the hardest part because they’ve NEVER been in that much pain for such a long time before and they simply can’t imagine what it’s like, and I’m sure it must be the same for you too. Most days I just want to give up for good. I can only take so much more before it all becomes too much.
I never asked for any this, and nobody even cares.
@nightblade628 I care and I totally understand. I'm so sorry you are experiencing this level of pain and doctor denial. I have been disabled from Fibromyalgia for 34 years, so I get it.
When I got Covid, then Long Covid, then Viral Meningitis, then Encephalopathy then Covid AGAIN -- ALL within the last three years, that really has led to horrendous pain. But also brain fog, aphasia, abnormal weight gain, light sensitivity, stimulus overload, blah, blah, blah, on and on. Keep on pursuing answers. You know already what they are likely to say. I understand that too. It sucks!! You be your own best advocate. I know it's super hard but write it all out little by little as you can tolerate. Best wishes to you. Never give up.
Great video. Thank you for the information. I am glad to hear you do the lumbar puncture test because you realize how bad it can get/ rule out bacterial meningitis. Most doctors will probably write it off as a migraine or the flu.
I had viral meningitis with severe encephalitis after having COVID19. At the hospital they did a CT scan, blood tests + lumbar puncture, I was hospitalized for 10 days to receive treatment. But you forgot to mention, the lumbar puncture usually causes more headaches until the body recovers the fluid that was taken out during the LP.
@MrsJey87 have you recovered? What where the symptoms because I think that’s what I have. Also got Covid
I think I have viral meningitis. I have severe headache and stiff neck for 3 days now. I am just realizing it may be meningitis. I had Covid 3 weeks ago. Thanks for sharing your experience.
Yes, a lumbar puncture may require a blood patch afterwards, because of a spinal fluid leak.
In my case, I got meningitis a year after Covid and Long Covid. How far apart were your two diagnoses?
Opposite from your experience, my headache was relieved by the reduction of CSF vis lumbar puncture. Less pressure on my brain. I got teary with relief! Meningitis pain is no joke.
This video was so helpful. Thank you for sharing and explaining viral meningitis. I think I may have this because I have a stiff neck and worst headache ever. I will see the doctor tomorrow.
How did things turn out for you? Did you have it? How was your recovery if so?
The human body should not be taken for granted or disrespected. Many don't listen or notice their symptoms pay attention to how you feel write down at what time it repeats. pain scale 1-10 .
I had viral meningitis 3 times in my life. 1st time I went to the ER.. they did a spinal tap. Told me I had the viral M. They sent me home with pain killers I recovered. The other 2 times I took pain meds until it cleared. Viral Meningitis can turn into Encephalitis which can be deadly..
When I was diagnosed, I was given antiviral meds. I wonder why you weren't?
What if you don't have fever???
In this series of educational videos I think it would be beneficial to show a spinal tap being performed. My reasoning behind this is that I feel some people may not be seeking treatment for their symptoms is fear of having this specific procedure performed. Please take this into consideration.
I was scared to have the lumbar puncture but was in so much pain and had been for so long (6 weeks undiagnosed in spite of 2 ER visits) that I was willing for anything. It was actually a blesséd relief to have some of that pressure removed from my brain via the lumbar puncture. They were very careful of my aftercare after the lumbar puncture - made sure I didn't move a muscle for two hours afterwards - so I had no bad side effects from it. They were great. Super grateful for those hospital staff that worked with me. ❤
My friends daughter has been diagnosed and hospitalized 4 times for viral meningitis and encephalitis
how long could a patient go with having this and not being diagnosed?
Did the person get sudden shakes who got meningitis
When I got meningitis my mind went from being very easy to remember short term memory things for test and I coukd retain and learn so easy but after I noticed I couldn't think howbi used to and wasn't as smart and when I trained for 3 months to work for at&t as a technical support agent and when we tok the exam you had to pass to become an agent it took me almost the whole time alloted as there was so much to remember and I was the one still testing and I never had problems passing test like that and that's how I used to pass classes was be a good tester but to me forever to recall everything I learned the previous 3 months and took forever remembering everything I learned and the pressure of the time slot also made me lose my ability to recall what I learned and I needed time to remember everything I learned and was just imagining wrong things before I took the time to recall tge facts. I knew I had brain damage than as my short term memory wasb
Shot as was my ability to rapidly learn what I was taught.
I have a question I had viral meningitis was in the hospital for a week on pain medications. I started sleepwalking and while I was in the middle of the sleepwalking my legs would give out and I would fall. And I also started which has lingered which has been year-and-a-half some days I cannot wake up and stay up the whole day I have to constantly sleep. I have seen to sleep specialist for and both of them tell me that that's not related however in Reading about viral meningitis and people's experience they have had the same problem. What would be your recommendation as my next step to try to find some help to be able to function properly awake because it's gotten to the point to where I can't even drive out of town because I'm afraid that I will crash. Any help you could give me would really be appreciated
My father in law faceing this problem… and our doctor gave us antibiotics.. but he didn’t eating properly.
ive been very tired i cant find anyone to help me or diagnnos me. ive hd it two times before. ive come down with it agian. i now have an antibiotic its also reccomended to take fish oil and ive noticed vit e helps alot. but we have no real doctors down here. im in central louisiana.
After meningo incefelities body vibraion,tiriedness will occur?
Can a spinal tap check for a meningitis that occurred weeks ago?
I had one that I think was maybe due to antidepressant medications. Because I felt very very ill during the 1st 3 days of treatment then stopped, and I felt gradually better. But felt very tired and exhausted for about a week (I was like "what ever this is; it's as if I had a very very bad flu". And during that time I strangely felt like having warm baths (I was having them multiple times a day; I didn't know why, I just felt like it and went and took a bath after a bath, then go to bed and reeeeeeesssssttttt. It was awful.
When I went to the psychiatrists they said it's normal to feel anxiety during the 1st days of using medications. But that wasn't any kinds of anxiety. I had photophobia, and sound phobia, I thought I was becoming autistic due to Prozac (I was searching for "Prozac induced autism", poor me, I felt like the SSRIs were irritating my CNS, as if someone was up there spraying fire at my brain)
When the I stopped the medications and the pain resided, I was unable to read and comprehend a thing, my IQ dropped, I turned from a smart person to a dumb person. I lost the ability to understand human emotions, I started to develop actual depression (I had a moderate depressive episode), I felt utterly squished from the inside out.
I went to the ER 2 times, and they said that I had nothing, they gave me lorazepam and propranolol for the "anxiety, agitation, and heart palpitations" I didn't take any of them. And just waited it out.
Ever since I lost the ability to sense time, didn't feel like my self, had depression, lost ability to use logic. And felt pressure behind my forehead that consided with these symptoms even after the pain went away. I wanted to see a neurologist but they kept saying that I should see a psychiatrist instead.
You are a very sensitive person, your reaction to medication could be because of a very sensitive gut, which is usually caused by food intolerance. May be you are gluten and dairy intolerant ? You should find a good naturopathic doctor and do the food sensitivities and toxicity level.
How long does it take to recover with memory loss from meningitis
I’ve had recurrent meningitis for over 30 years. It’s awful & there is no cure. Cannot count how many times I’ve had it. The after effects are horrible. It gets worse with each episode.
Is viral or bacterial meningitis contagious, and if so how is it transmitted?
great question...I will reply through my facebook page DrERTV.
PatientEducation.Video thanks Doctor
This is a very serious condition indeed Doctor
TAVOR VICEROY VALDOR please give information after recovey how to take care viral meningities
i had viral herpes meningitis in april. im recovering now... do i feel ever 'normal' again? like not tired anymore and strange in my head?
what was the symptoms?>
Currently in the hospital for viral meningitis
Shit i think i have viral meningitis.
Head banging. Shivers. Burny eyes. Dizzy.nauseous.
I hate this sickness so much I lost my very childhood best friend with this why the doctors didn’t know it was meningitis it was too late he was comatose then die in 5 days why they didn’t know until it’s late they said he was on drugs because he forgot things? I’m just so hurt it was too quick Doc .
A lot of them don’t care and will actually hurt the patient more
@@lowkeyrings9221 Yeah seriously being healthy is such a lucky thing docotor dont understansd their own luck
I had been attacked by a cute meningitis from 22nd of the December 2019 and treatment to Dr.Rahul Prasad till now but I could not walk freely .
Please let me know after how many days I will walk freely?
My CT scan Report is normal.
Permanent nerve damage
How do you tell the difference between meningitis and a migraine?
I will reply on my DrERTV FaceBook page! check it out
PatientEducation.Video reply
How do you tell the difference between meningitis and a migraine?
Jennifer Ferguson hi, I've been in hospital and treated for viral meningitis twice and I've suffered migraines all my life. The main difference I can say with me was the fever I had a temperature of 40c to 42c at the recorded highest and I was delirious, I felt generally unwell and just wanted to be left alone I had the splitting headache dizzyness and photosensitivety and I was very very sensitive to any noise. With migraines I've learnt they are very person specific and if it's something you've never felt before or it's unusual for you normal pattern then seek help asap! X