Eye Care :: Neurocysticercosis On Left Optic Nerve - No Improvement
Feb 27, 2016
I m diagnosed neurocysticercosis on left optic nerve n m having blurring of vision.
Drs have put me on steroids past one year ,but no Improvement is seen.
Feb 27, 2016
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Eye Care :: Optic Nerve Been Blocked - No Treatment
My mother can't see anything clearly for 3 to 4 years. Doctor says that her eyes nerve are been blocked.
View 1 RepliesNeurological Disorders :: Discolouration On Optic Nerve With Septo-Optic Dysplasia
I have Septo-optic dysplasia, and I'm lucky if I ever get to see someone who's even heard of it because it's apparently one of those rare and awkward conditions with varying symptoms. But basically, in my case, the nerves in my eyes didn't develope well or at all.
I have 6/60-6/48 vision in my right eye and 0 in my left eye; as in I don't even see black or anything at all. I don't think light could ever get in there.
My most recent check up at the Optician showed some discoloration on the optic nerve in my left eye (the blind eye). It appeared black, apparently, which my Optician said meant it had been there a long time, as opposed to grey? But no one seems to know if this is normal for an optic nerve that never formed properly.
Apparently the discoloration is not mentioned in any of my letters on record, though. Is that weird? That's the only thing making me worried. Some people say it should be obvious so not included, but others say that means it's new?
Eye Care :: Elevated Optic Nerves
I am a sixty year old female and went for my annual eye exam. I was told by my optometrist my left eye optic nerves were elevated - OS>OD. Also has irregular Mac. OS. She had her nurse call and make an appointment for me to see an Ophthalmologist tomorrow. I had a Brian MRI in December and the report reads. "There is nonspecific mild focal areas of bilateral supratentorial which is commonly secondary to chronic microvascular ischemia. MS seems less likely, but cannot be excluded".
I have intermittent headaches only on the left side and at times feel nauseous. Should I be concerned?
Eye Care :: Optic Nerves In My Eyes Are Swollen
I went and do a check up on my eyes and the optic nerves in my eyes is swollen ...I did a CT scan and the results was clean...so I want to know what causes the swelling.
View 2 RepliesMultiple Sclerosis :: Thin Optic Nerve
Just back from an eye appt and was told that my (L) optic nerve is thinning and my field vision test was normal.
I have not had any loss of vision or blurriness other than the blurriness that comes with my migraines. Is it possible to have optic neuritis w/o it affecting your vision?
I have to wait until 7/19 to see my neuro, so I am still waiting to be diagnosed, however, the news I was given this morning makes me lean more towards MS.
Multiple Sclerosis :: Wandering Eye After Optic Nerve Neuritis
Was cross eyed as a child. One surgery on left and 2 on right 57 year old male. Surgery at 6 10 and 20. Had about 5 bouts of optic nerve neuritis about 15 years ago. Both eyes but more serious in rt eye. No MS. MRI every year for 5 every other since. Now my right eye wanders up and out all the time contacts and glasses do not help much. My vision came back fine other than age stuff. I Want to know why my eye wanders up and out and is there anything I can do for it ? Is it from old surgeries? Is it from optic nerve?
View 1 RepliesEyes :: Damage To Optic Nerve - Light Headed With Floaters
I was having frequent headaches and occasionally feeling lightheaded with floaters. I went to the opticians and they referred me to the ophthalmologist who put eye drops in and said that at the back of my left eye the optic nerve was sheeted. (I don't understand what this term means and cannot see anything on the internet to explain either) He just said that I didn't have any other symptoms for Optic Neuritis and wasn't sure but didn't think it was anything sinister. I am now waiting for a scan of the eye to see what that shows.
However, the last couple of weeks I have been getting pins and needles all over my body, mainly in arms and legs. I've also had general aching pains.
I have read online about symptoms and they point to all kinds of things, Fibromyalgia, Anxiety and possibly MS. As you can imagine this has really scared me as I have read that problems with the optic nerve can also be related.
Has anyone else had these symptoms or are they too few for me to be making assumptions?
Cerebral Sinus Thrombosis - Tension Headaches And Optic Nerve Damage
I'm 32. It was only detected after suffering 2 weeks of intense headaches which eventually affected my optic nerves in my eyes. I wear glasses and after 2 weeks of intense headaches my eyesight actually became much better which baffled me. I was sent away from GP with the diagnosis of a tension headache (which I don't hold any blame for) but luckily I pursued further and booked an immediate appt with an Optician who found that my visual field was affected in my left eye. I was advised to go to the Emergency Eye Casualty who continued with further tests on my eyes. They discovered the damage to my optic nerves but at this point were unable to find the source and I was seen immediately by a Neurologist who at first thought it was benign cranial hypertension. He arranged a CT scan and said that he did not expect to find anything but was very surprised to see the clot on the CT. I was admitted immediately and underwent a lumber puncture. I spent 5 days in hospital and was discharged on Warfarin medication for 3 months. I have since undergone a repeat CT scan. I believe I was very lucky as any longer I could have had a stroke. I was advised to stop the oral contraceptive pill immediately as they said this may have been the cause but also that I have recently underwent a breast reduction 3 months before.
View 44 RepliesVestibular Neuritis - Vestibular Nerve On My Left Side With 80% Weakness
2 years ago I had gotten a bad ear infection after a trip to Disney from pool is what doctors believe. It was misdiagnosed at first so it severely damaged my vestibular nerve on my left side with 80% weakness. Of course this was all found out after the slew of mri's, mra's, various vestibular testing, color/hot water in ears etc. 6 months of testing and 2 rounds of vestibular therapy have not helped me at all. I am on my 4th
specialist in NYC who finally put me on acetazolamide for the sick side effects of nausea and brain fog. 6 months into these pills and now my body is starting to become accustomed to them and are not working so well. My symptoms are
1) Overall unsteadiness and dizziness (fall to the left)
I work in NYC so my commute walking is the worst, shopping too.
2) Brain Fog - how else to explain this just a horrible feeling in my head
constantly that very rarely feels better.
3) Nausea (without the pills I could just be laying in my bed and fell like
I am going to throw up)
4) Disgust and Depression over this whole mess I am only 51.
I am told by many doctors 95% of people recover, right side compensates for the left side over time. This has not happened at all. I also have never heard of anyone having it constantly for this long. Can someone at least tell me they are the same?
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just wondering if anyone here has a reverse T3 problem and if so, how long did it take before you saw an improvement in symptoms after taking medication?
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I'm 30 yrs old and i have a left-eye amblyopia. I undergone squint surgery last year's August. My eye barely improve and i really feel very down because i was expecting my eye will be at last okay but it didn't. The surgeon said it will require my right eye (which is okay) if i want further improvement in my left eye. I want to know what's will be the downside once my right eye get operated. Please help! My surgeon doesn't talk too much aside from telling me what else i need to do. I really wanted my left eye to be aligned correctly as greatly as possible. I suffered too much.
View 2 RepliesUlcerative Colitis :: Remicade - Any Improvement?
Just wondering how long it took people to get any kind of improvement in their colitis symptoms with renicade. I had my first loading dose today and the dr said it would take some time to see any kind of result.
Also did you experience any itching or headaches after? About two hours after i started expiencing itchy eyes and started to get a headache, now 8 hrs after the infusion finished my hands, arms and face are itchy. My eyes are still itchy and my headache is still there.
I had an allergic reaction to 6mp but it was far more intense itching than this.
Rheumatoid Arthritis :: Any Improvement With Antidepressants?
I've reluctantly started Zoloft (SSRI antidepressant), being encouraged to do so by my GP due to the depression of diagnosis and the possibility I also have fibromyalgia.
(Pain isn't just limited to joints and fatigue is crippling) ie: I've slept 18 hours of the last 24 and still so very tired.
I'm having awful start up side effects which I understand will pass and understand there will be no benefit until 4-8 weeks, if at all.
I've tried Lexapro a while back with no real success.
Has anyone had any improvement at any level with ADs? I really hate mucking around with my brain chemistry.
No Change / Improvement In Hearing After Stapedectomy
I was virtually deaf in one ear and very little hearing in the other ear, have worn hearing aids for 25 years. Recently (all happened so quickly, within 6 weeks) got diagnosed with Otosclerosis in both ears. 6 weeks after seeing doctor, i had the op. I had a stapedectomy/stapedotomy on 04/01/2016. Noticed a faint improvement in hearing when lying on the ward after the op, could faintly hear trolleys being moved about. But nothing drastic...... I've had dizziness, (not room spinning dizziness) which now only remains if i read, do jigsaws, scan shop shelves from side to side etc, weird! I've been through the heart pulsating, creaking, the rain dripping onto a metal plate sound etc.
I've had no real explanation of what to expect, i didn't really ask the surgeon any questions as i wasn't sure what would happen after and was unaware i'd have so many unanswered questions come up.
I assumed, and read some on the internet, and was told by a friend who'd had it done, that once the packing was removed, i'd be able to hear. Had packing removed 6 days ago, i'd built myself up SO much, that i stood and sobbed when i still couldn't hear! Surgeon looked a bit puzzled, but he said he wasn't worried at this point and to see him again in 6 weeks and that it'd be fluid behind my ear. He said i need to have some popping before i'll hear.
So, here i am now, with no change in my hearing for the last 6 days. I'm sure when i swallow, i sound as if fluid is in there? I also get like a thunder noise mainly in the morning when i wake up and my throat moves. But what's worrying me most after reading up on the internet again, is when i put headphones on, i can hear the music, (have to have it on loud to hear it), but the loud thumps/beats in the music make my ear crackle like a loose wire on a radio. I read last night that this is because the op hasn't worked and the prosthesis needs tightening/shortening/revising. But then on the other hand i've read that this may be normal?
If i go to do a burp movement when i have music in the headphones, i get a millisecond of a loud noise, but then it goes again as my throat can't seem to hold the noise open if you get what i mean. I have soooo many questions but don't want to bore you with them, maybe later. So, should i be hearing by now, is the crackling loose wire sound normal, and if you have any other advice that might stop me worrying please. I'm just sitting waiting day by day thinking today might be the day that i hear.
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The doctor prescribed me Trimethoprim 300 Mg for 7 days. I am having it since last 3 days now but nothing has improved.
The dipstick test showed blood in my urine...though I have been having some other health issues as well...but this medicine was prescribed when the urine sample had blood.
I am worried that I might be having the wrong medicine, as nothing is improving.
I need to understand, how long should I wait for the improvement signs. I am worried. I feel dizzy after this medicine, and my health is getting worse.
Amiodarone 200 Mg For Atrial Fibrillation - Marginal Improvement
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View 7 RepliesAnkle :: Torn Ligaments And Tendons Surgery - No Improvement
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After what feels like a lifetime of side effects and then nothing, I think things are looking up. Had a great day today, and I haven't said that in a while, particularly on a Monday. I have counted hours, days and weeks. Like everyone else I have questioned my dose and the medication on many occasions and felt like giving up a million times. To everyone who encouraged me to keep going and give it time, thank you, because it does get better in its own good time. I have no doubt that there will be ups and downs to come, but hey, I think I'm going to make it! Yes it really has taken 20 mg this long to start to work on my head , so keep at it during the early weeks. I hope everyone is letting a little more light in every day.
View 50 RepliesVascular Disorders :: Numb Left Leg And Strange Scars On Left Side Of Stomach
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View 1 RepliesOptic Neuritis - Eye Sight Getting Worse
I have worn glasses all my life and always been dependant on them. I was having trouble with my vision so decided to have my eyes checked out again, although i only had a sight test nine months ago. It resulted in me requiring stronger glasses and a large increase in both eyes, especially my left eye. I have a difference of 1.75 between my left and right eye.
I was referred onto the eye specialist again for further checks and i was told i have Optic Neuritis, and was told that my eyesight will probably get worse and been advised to return to the opticians in a few months to have them checked out again.
I was prescribed last year additional reading lenses i wear multifocal contact lenses most of the time but wear my glasses at night. I was advised by the opticians that my prescription is pretty strong especially needing additional reading help.