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Snoo
I have had PMR for many years and am in fact now labelled inflammatory arthritis. The signs and symptoms are the same as is the treatment on and off Pred. I had shingles badly about three years ago and this year will qualify for the shingles vaccine. Has anybody had the vaccine while on Pred and were
I have had PMR for many years and am in fact now labelled inflammatory arthritis. The signs and symptoms are the same as is the treatment on and off Pred. I had shingles badly about three years ago and this year will qualify for the shingles vaccine. Has anybody had the vaccine while on Pred and were
Snoopy7
in
PMRGCAuk
3 years ago
Small Molecules, STARs Treat Cell Models of GBA1-linked Parkinson’s
For Parkinson’s, the cells were engineered into dopaminergic neurons (nerve cells that make the signaling molecule dopamine), as this disease is caused by the
death
and dysfunction of these neurons in the
brain
.
For Parkinson’s, the cells were engineered into dopaminergic neurons (nerve cells that make the signaling molecule dopamine), as this disease is caused by the
death
and dysfunction of these neurons in the
brain
.
Hidden
in
Cure Parkinson's
3 years ago
Viral meningitis
I have had VM, unfortunately the virus was not a usual strain so I did not respond to any IV treatments they usually give to VM patients. I had to fight it myself with a temp of 40.2. How long will the headaches last? Been in hospital 3 weeks only recently discharged and scared for the future .Any advice
I have had VM, unfortunately the virus was not a usual strain so I did not respond to any IV treatments they usually give to VM patients. I had to fight it myself with a temp of 40.2. How long will the headaches last? Been in hospital 3 weeks only recently discharged and scared for the future .Any advice
UptoonGirl1
in
Meningitis Now
3 years ago
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Does shingles cause Hashimoto’s to flare up?
I have had Hashimoto’s now for about 3 years and I’m still finding it hard navigating my way through the symptoms and flare ups. I have suffered from very bad crippling anxiety over the last year and half which hasn’t helped with the lockdown and dealing a 4 year old and 1.5 year old while attempting
I have had Hashimoto’s now for about 3 years and I’m still finding it hard navigating my way through the symptoms and flare ups. I have suffered from very bad crippling anxiety over the last year and half which hasn’t helped with the lockdown and dealing a 4 year old and 1.5 year old while attempting
Purple_dog
in
Thyroid UK
3 years ago
Lyme's Disease long term arthritis
Is there anyone out there who has long term joint issues due to Lyme's Disease. I had it in 2019 but now struggle to walk 1 mile due to my knees apparently having crumbled and I have cysts on the cartlidge too. Is anyone having similar problems please ? Any advice too thanks.
Is there anyone out there who has long term joint issues due to Lyme's Disease. I had it in 2019 but now struggle to walk 1 mile due to my knees apparently having crumbled and I have cysts on the cartlidge too. Is anyone having similar problems please ? Any advice too thanks.
Bessie22
in
Pain Concern
3 years ago
MrHave PMR currently reducing am on 8mg...now have shingles should I increase pred?
PMR and Shingles
PMR and Shingles
Devon21
in
PMRGCAuk
3 years ago
The Brain Tumour Charity support teams now on Instagram!
Alongside the charity's main Instagram account, we have launched a dedicated support account - @thebraintumourcharity_support Follow us to find out more about our services, as well as information and advice to help you cope with a brain tumour diagnosis. https://www.instagram.com/thebraintumourcharity_support
Alongside the charity's main Instagram account, we have launched a dedicated support account - @thebraintumourcharity_support Follow us to find out more about our services, as well as information and advice to help you cope with a brain tumour diagnosis. https://www.instagram.com/thebraintumourcharity_support
Shannon_TBTC
Partner
in
Acoustic Neuroma Support
3 years ago
FUS vs. DBS An interesting debate on twitter
Expert's favour DBS over FUS
Expert's favour DBS over FUS
Farooqji
in
Cure Parkinson's
3 years ago
Lot of questions re DBS lately. Everything you could want to know.
Chapter 1 Introduction to Surgical Therapies for Parkinson’s Disease ............4 Chapter 2 An Overview of Deep Brain Stimulation (DBS) Therapy...............8 Chapter 3 Risks and Complications of DBS ..................................................19 Chapter 4 Is DBS Right for You? ...........
Chapter 1 Introduction to Surgical Therapies for Parkinson’s Disease ............4 Chapter 2 An Overview of Deep Brain Stimulation (DBS) Therapy...............8 Chapter 3 Risks and Complications of DBS ..................................................19 Chapter 4 Is DBS Right for You? ...........
MBAnderson
in
Cure Parkinson's
3 years ago
DBS for Parkinsons
Need a little info on the DBS surgery for Parkinson’s. Doc says our daughter has reached the limit for the Sinemet dosage and is beginning g to show signs of needing more help. The only thing left is DBS. She’s not worried about the actual surgery but the cost since her insurance won’t cover very much
Need a little info on the DBS surgery for Parkinson’s. Doc says our daughter has reached the limit for the Sinemet dosage and is beginning g to show signs of needing more help. The only thing left is DBS. She’s not worried about the actual surgery but the cost since her insurance won’t cover very much
Williemom
in
Positive Wellbeing During Self-Isolation
3 years ago
Dbs lottery?
Dbs lottery
Dbs lottery
Abepark2013
in
Cure Parkinson's
3 years ago
DBS lottery
Whilst I’ve read dozens of posters extolling the virtues of DBS here on the site and have witnessed many stories on YouTube similarly telling of good things, the PWP that I know personally who’ve had it haven’t been so encouraging. 😕 Guy 1 was hoping to reduce his meds but has ended up taking the
Whilst I’ve read dozens of posters extolling the virtues of DBS here on the site and have witnessed many stories on YouTube similarly telling of good things, the PWP that I know personally who’ve had it haven’t been so encouraging. 😕 Guy 1 was hoping to reduce his meds but has ended up taking the
jeeves19
in
Cure Parkinson's
3 years ago
Theranostics Promising article, I'd like to hear feedback from the Forum. Does anybody else have experience with this treatment,
He is developing molecules at the Loma Linda clinic that he hopes in the future can be sent in to find and treat breast cancer and glioblastomas, currently a
death
-sentence
brain
cancer. "This is exciting. It's very exciting." he said. "We can win this war." COURTESY OF LOMA LINDA UNIVERSITY
He is developing molecules at the Loma Linda clinic that he hopes in the future can be sent in to find and treat breast cancer and glioblastomas, currently a
death
-sentence
brain
cancer. "This is exciting. It's very exciting." he said. "We can win this war." COURTESY OF LOMA LINDA UNIVERSITY
Zzzgott
in
Advanced Prostate Cancer
3 years ago
Stress triggering meningitis
What are your thoughts on stress being a trigger for a viral infection and triggering viral meningitis and M.E? Do you think stress plays a contributing factor?
What are your thoughts on stress being a trigger for a viral infection and triggering viral meningitis and M.E? Do you think stress plays a contributing factor?
Sunny308
in
Meningitis Now
3 years ago
Hydrocephalus post Cranioplasty
Hi, my daughter had a brain injury last year. She had a craniectomy and had a cranioplasty in October. For the last month or so, she has woken with a severe headache several times. Twice in the last week. Plus in the last month she’s started with balance problems. She looses her balance when walking
Hi, my daughter had a brain injury last year. She had a craniectomy and had a cranioplasty in October. For the last month or so, she has woken with a severe headache several times. Twice in the last week. Plus in the last month she’s started with balance problems. She looses her balance when walking
Kezza72
in
Headway
3 years ago
My story of trying to find a get the right treatment
My name is lanelle Hardwick and I live with a pineal cyst and a bilobed cyst on my brain. It is so frustrating trying to get across to the health department of this expertise, I am currently in the public system of neurological wait list as catergory 2 and I am constantly suffering symptoms of headaches
My name is lanelle Hardwick and I live with a pineal cyst and a bilobed cyst on my brain. It is so frustrating trying to get across to the health department of this expertise, I am currently in the public system of neurological wait list as catergory 2 and I am constantly suffering symptoms of headaches
lannelle
in
Headway
3 years ago
Chronic Shingles & Hashi/Hypo
Anyone else get Shingles everytime their TSH rises due to Hashi’s & it’s time for an increase in Levo.mg’s? This has been my pattern for a year now. First round was face/neck second was armpits. Both times bilateral. Shingles vaccine has not been an option for me because I can’t go long enough in between
Anyone else get Shingles everytime their TSH rises due to Hashi’s & it’s time for an increase in Levo.mg’s? This has been my pattern for a year now. First round was face/neck second was armpits. Both times bilateral. Shingles vaccine has not been an option for me because I can’t go long enough in between
badgenes
in
Thyroid UK
3 years ago
DBS, good or bad thing?
I've decided to take the plunge on dbs, the meds don't work much anymore and side effects are kicking my butt. it's been 7 yrs since diagnoses, unbelievable suffering everyday. Your thought's, pros and cons, warnings, tips , suggestions, secrets ect. .thank you greatly
I've decided to take the plunge on dbs, the meds don't work much anymore and side effects are kicking my butt. it's been 7 yrs since diagnoses, unbelievable suffering everyday. Your thought's, pros and cons, warnings, tips , suggestions, secrets ect. .thank you greatly
Hidden
in
Anxiety and Depression Support
3 years ago
Links to some articles comparing FUS to DBS for Essential Tremors
For the time being, there's more research and development in the ET field than the PD field as it relates to tremor dominant Parkinson's. Here's a few links that compares the two. https://www.neurologyreviews-digital.com/neurologyreviews/nr_march_2019_/MobilePagedArticle.action?articleId=1470923
For the time being, there's more research and development in the ET field than the PD field as it relates to tremor dominant Parkinson's. Here's a few links that compares the two. https://www.neurologyreviews-digital.com/neurologyreviews/nr_march_2019_/MobilePagedArticle.action?articleId=1470923
pdpatient
in
Cure Parkinson's
3 years ago
DBS - yes or no?
How to decide on a DBS placement I'm gonna take the plunge. I just cant do the meds anymore, they don't work like they used to and I'm beyond miserable. Any thoughts or suggestions?
How to decide on a DBS placement I'm gonna take the plunge. I just cant do the meds anymore, they don't work like they used to and I'm beyond miserable. Any thoughts or suggestions?
Hidden
in
Anxiety and Depression Support
3 years ago
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