Experiences with Neurosurgery | HealthUnlocked

702 public posts

Neurosurgery

Pain the feet and legs 1 year after spinal surgery, it also affects my blabber.Help.Pain the feet and legs 1 year after spinal surgery, it also affects my blabber.Help.

nanapat112in Pain Concern

6 months ago

Treatment at the national hospital for neurology and neurosurgery

The treatment at the national hospital of neurology and neurosurgery has been very successful on several levels. I'm not better, but I'm much better than I was and I now have a greater understanding of what's going wrong.The treatment at the national hospital of neurology and neurosurgery has been very successful on several levels. I'm not better, but I'm much better than I was and I now have a greater understanding of what's going wrong.

BuntyPin Functional Neurological Disorder - FND Hope

4 months ago

Treatment for bladder, bowel and sexual function

Conditions treated We treat the following conditions: Neurogenic and idiopathic detrusor overactivity Non-urological urinary retention Fowler's Syndrome Referral contact address: Uroneurology Dept The National Hospital for Neurology and Neurosurgery Queen Square London WC1 3BG Telephone: 020 3448Conditions treated We treat the following conditions: Neurogenic and idiopathic detrusor overactivity Non-urological urinary retention Fowler's Syndrome Referral contact address: Uroneurology Dept The National Hospital for Neurology and Neurosurgery Queen Square London WC1 3BG Telephone: 020 3448

wobblybeein Ataxia UK

2 months ago

National Hospital for Neurology and Neurosurgery, London - Anyone been?

Looks like I have been referred to the ‘National Hospital for Neurology and Neurosurgery’ in London (wasn't sure if I'd be referred here as was waiting), and I just wondered if anyone has been to this place, either for MDT meetings, or for treatment?Looks like I have been referred to the ‘National Hospital for Neurology and Neurosurgery’ in London (wasn't sure if I'd be referred here as was waiting), and I just wondered if anyone has been to this place, either for MDT meetings, or for treatment?

MikeMein Brain Aneurysm Support

7 months ago

The Patient Voice

Hi all This is a link to my vlog about my recent visit to the National Hospital for Neurology and Neurosurgery. https://youtu.be/kx9aRLQlmck Cheers, IanHi all This is a link to my vlog about my recent visit to the National Hospital for Neurology and Neurosurgery. https://youtu.be/kx9aRLQlmck Cheers, Ian

Ianfrizellin Parkinson's Movement

a year ago

Neurotrophic Factors Update: "Improvement of 100%"

." - Steven Gill, MB, MS, FRC "Researchers used robot-assisted neurosurgery to implant a specially designed delivery system, termed Convection Enhanced Delivery (CED), which allowed high flow rate infusion to be administered to patients every 4 weeks.." - Steven Gill, MB, MS, FRC "Researchers used robot-assisted neurosurgery to implant a specially designed delivery system, termed Convection Enhanced Delivery (CED), which allowed high flow rate infusion to be administered to patients every 4 weeks.

PDConsciencein Parkinson's Movement

9 months ago

Pseudoprogression.

PMID: 31830211 DOI: 10.1001/jamaoncol.2019.4636 [2] https://www.ncbi.nlm.nih.gov/pubmed/29618107 Neurosurgery. 2019 Mar 1;84(3):647-654. doi: 10.1093/neuros/nyy075.PMID: 31830211 DOI: 10.1001/jamaoncol.2019.4636 [2] https://www.ncbi.nlm.nih.gov/pubmed/29618107 Neurosurgery. 2019 Mar 1;84(3):647-654. doi: 10.1093/neuros/nyy075.

pjoshea13in Advanced Prostate Cancer

a month ago

Connecting

My hubby had neurosurgery 20 years ago and all this time we have lived with his epilepsy, low empathy and mood and anxiety. He shouts a lot at me, has no life, energy, motivation or interest in changing his situation.My hubby had neurosurgery 20 years ago and all this time we have lived with his epilepsy, low empathy and mood and anxiety. He shouts a lot at me, has no life, energy, motivation or interest in changing his situation.

Violet-flamein Headway

a year ago

Polycythemia + Brain Tumor - Update

The treatment team at Johns Hopkins Hospital included the Director of Neurosurgery, the Director of the MPN Clinic, The Director of the Neurofibromatosis Clinic , and my regular care doctors.The treatment team at Johns Hopkins Hospital included the Director of Neurosurgery, the Director of the MPN Clinic, The Director of the Neurofibromatosis Clinic , and my regular care doctors.

hunter5582in MPN Voice

7 months ago

Airing Pain 115: Neuropathic Pain (part 1 of 2): Targeted Pain Managment Programmes

More Information: Neuropathic Pain – Explanations and support at The National Hospital for Neurology and Neurosurgery Pain Management Centre in London. https://www.uclh.nhs.uk/OurServices/ServiceA-Z/Neuro/PMC/Pages/Home.aspxMore Information: Neuropathic Pain – Explanations and support at The National Hospital for Neurology and Neurosurgery Pain Management Centre in London. https://www.uclh.nhs.uk/OurServices/ServiceA-Z/Neuro/PMC/Pages/Home.aspx

PainConcernProjectsAdministratorin Pain Concern

6 months ago

PSP and Hydrocephalus

Hi, I'm new here and appreciate My husband has both PSP and Hydrocephalus. The hydro was diagnosed first, and he got a shunt in the fall of 2018, clearing up the symptoms almost right away (headaches, fuzzy thinking, incontinence, balance). Nine months later, I began noticing changes...first his gazeHi, I'm new here and appreciate My husband has both PSP and Hydrocephalus. The hydro was diagnosed first, and he got a shunt in the fall of 2018, clearing up the symptoms almost right away (headaches, fuzzy thinking, incontinence, balance). Nine months later, I began noticing changes...first his gaze

Hukiluin PSP Association

6 days ago

Another hurdle over

It's 15 weeks since my ruptured aneurysm and 3 hr operation to coil it. Today I travelled 1 and 1/2 hrs for my first appointment with the neurosurgeon. Last night a new feeling manifested itself. I Became very anxious about the appointment even though it was just a meeting. It's the first time I haveIt's 15 weeks since my ruptured aneurysm and 3 hr operation to coil it. Today I travelled 1 and 1/2 hrs for my first appointment with the neurosurgeon. Last night a new feeling manifested itself. I Became very anxious about the appointment even though it was just a meeting. It's the first time I have

Rudchesterin Headway

11 days ago

My tinnitus and one sided deafness (caused by massive brain tumour) story.

Hello my name is Ivan and my story starts in summer 2018 when I was on holiday abroad and I noticed my hearing in my right ear was significantly worse than normal. I assumed this was due to a water being stuck in my ear canal (as it happened 3 or 4 times before) and didn't pay much attention to it asHello my name is Ivan and my story starts in summer 2018 when I was on holiday abroad and I noticed my hearing in my right ear was significantly worse than normal. I assumed this was due to a water being stuck in my ear canal (as it happened 3 or 4 times before) and didn't pay much attention to it as

Ivan123in British Tinnitus Association

18 days ago

Checking in with the"old-timers"!

Hi Heady, Eastern Cedar, and all my dear friends on this site. I was checking in saw Heady's post on getting together. I have to admit I was envious of all of you being able to do so. I have been busy here in the states. I am happy! Truly. Never thought I would feel right again but one day my lifeHi Heady, Eastern Cedar, and all my dear friends on this site. I was checking in saw Heady's post on getting together. I have to admit I was envious of all of you being able to do so. I have been busy here in the states. I am happy! Truly. Never thought I would feel right again but one day my life

goldcapin PSP Association

20 days ago

Update - PV + NF1-Brain Tumor + Even more excitement!

Hoping the new year finds you all well and looking forward to happiness and success in the coming year. Decided it was time to post an update on the ongoing saga of managing PV along with various and sundry other issues. History - The current saga starts back in January 2018 when I had a god-awfulHoping the new year finds you all well and looking forward to happiness and success in the coming year. Decided it was time to post an update on the ongoing saga of managing PV along with various and sundry other issues. History - The current saga starts back in January 2018 when I had a god-awful

hunter5582in MPN Voice

21 days ago

Well I never

Discs gone in neck from C2 3 4 5 6 and 7 with bilateral stenosis at c3 4 ŕight side foramen and bilateral stenosis at C4 5 left side foramen....symptoms have been going on for years! Have been over the years diagnosed with Raynards ME urge/stress incontinence carpal tunnel syndrome (operation to releaseDiscs gone in neck from C2 3 4 5 6 and 7 with bilateral stenosis at c3 4 ŕight side foramen and bilateral stenosis at C4 5 left side foramen....symptoms have been going on for years! Have been over the years diagnosed with Raynards ME urge/stress incontinence carpal tunnel syndrome (operation to release

Angelicscripts6in Cervical Myelopathy

23 days ago

Update from my last post of neurosurgeon appointment

Saw the surgeon this afternoon and he informed me that after looking at ct scan and xrays that were done this past October that he’s telling me as of right now he’s not going to operate on my shunt. He thinks everything is okay like it is. He said most likely it’s calcification that I’m feeling that’Saw the surgeon this afternoon and he informed me that after looking at ct scan and xrays that were done this past October that he’s telling me as of right now he’s not going to operate on my shunt. He thinks everything is okay like it is. He said most likely it’s calcification that I’m feeling that’

JDQuinn75in Epilepsy Action

24 days ago

Neurosurgeon appointment

Happy New Year to all. Tomorrow afternoon I have an appointment with a neurosurgeon to figure out what to do with the pain I’ve had numerous times . Each time it’s started where my shunt starts and tracks all the way down the side of my neck. Two years ago I found out that it’s discontinuous down theHappy New Year to all. Tomorrow afternoon I have an appointment with a neurosurgeon to figure out what to do with the pain I’ve had numerous times . Each time it’s started where my shunt starts and tracks all the way down the side of my neck. Two years ago I found out that it’s discontinuous down the

JDQuinn75in Epilepsy Action

25 days ago

Met in c5 c6 :-(

Now on Olaparib off Xtandi ...psa rose to 4.8. But, met in C5 C6 area is really painful. Pain in my neck, left shoulder, arm and fingers are tingly. Very limited motion now in my left arm. CT scan showed narrowing ... thanks to my wonderful PCa onologist, I got into a neurosurgeon right away. HeNow on Olaparib off Xtandi ...psa rose to 4.8. But, met in C5 C6 area is really painful. Pain in my neck, left shoulder, arm and fingers are tingly. Very limited motion now in my left arm. CT scan showed narrowing ... thanks to my wonderful PCa onologist, I got into a neurosurgeon right away. He

Alvin735in Advanced Prostate Cancer

a month ago

Bullseye maculopathy

Hi I’ve just joined. I’m 52 and I’ve had a rough year with having brain surgery, just found out on Friday that I have this bullseye maculopathy so I don’t really know much about it. Just wondering can people please tell me what treatment they do. I’m in Australia. ThanksHi I’ve just joined. I’m 52 and I’ve had a rough year with having brain surgery, just found out on Friday that I have this bullseye maculopathy so I don’t really know much about it. Just wondering can people please tell me what treatment they do. I’m in Australia. Thanks

Catharinemcin Macular Society

a month ago

1
2
...
36
Next page