The Neurology Academy is an innovative education provider for clinicians, specialist nurses and professions allied to medicine. The training program focus is on both disease management and service transformation. Each priority condition is led by an Academic Faculty of practicing clinicians who operate within a separate disease focussed Academy. Course attendees improve their own understanding in management of the condition as well as working towards improvements in their own local services through audit, data, education and networking.
Current Academy priorities are Multiple Sclerosis, Parkinson’s Disease, Dementia, Epilepsy and Headache Disorders.
Many would say this is too good to be true, I must say this real quick that it is very good and very true how Dr Madida Sam on RU-vid cured my Parkinson Disease with their PD treatment protocol🌱🌱🌱/
We really need to find a new alternative from these ancient test TYM and the ACE-R test. Professionals are using them as a final test, not an assessment. The problem being, you can have Alzheimers, be really smart and pass. Not have Alzheimers, not be the brightest and fail. Then you have Alzheimers 😮.
I've read Tributyrin is superior to Butyrate. Can you say why this is? I took butyrate with bacillus but experienced some abdominal discomfort. I wasn't going in from scratch I've been working on these issues for many years with nutrition support. Are these butyrate or Tributyrin better used with or without food?
I am not only happy am alive but also glad that "DrMadida" was able treat and cure me with his herbal medication of my parosmia, Meniere disease and Parkinson disease(PD) with their herbal treatment. My smile is so bright because I am happy ‘’
“I am not only happy am alive but also glad that "DrMadida" was able treat and cure me with his herbal medication of my parosmia, Meniere disease and Parkinson disease(PD) with their herbal treatment. My smile is so bright because I am happy .”
Parkinson disease 🦠 🦠is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine from Dr Madida that truly works that helped treat, cure and reversed all his symptoms…My Dad is well a gain.
My prayers are with you all and I know how you all feels, my Dad suffered same illness for 13 years until madida herbal center came to his aid and cured him with their natural PD herbal medicine, Click and search #DrMadida, and let your Parkinson Disease be taken care of and be cured just same way my Dad’s own was taken care of and cured👌👌.
Great things Dr Madida on RU-vid has being doing for mankind, I undergo his Parkinson disease treatment plan for weeks and my Parkinson Disease was completely reversed///
Parkinson disease is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine that truly works that helped treat, cure and reversed all his symptoms••My Dad is completely okay and healthy now…
By the bone pain from Granix shots leading up to collection day was brutal! I knew it must have been time because the pain was Terrible and luckily it was 😊
I love what you do for MS I just wish the NHS would actually do something about your comments, since COVID we are just left to die ! The NHS is seriously dysfunctional it’s like have a performance engine that isn’t connected to the steering or transmission 🙁
Many don’t believe that Parkinson Disease, PTSD or DID can be reverse treated and cured, all they believe is that there is no cure but I am glad letting you all know that it is all wrong because my friends Mom that has being sick with Parkinson Disease for years just got her Parkinson Disease and her husband's PTSD reversed and cured with a herbal supplements from DR MADIDA on RU-vid.
Hi, I have had 9 lots of tysabri and my 2nd dose of optic neuritus. I am in a lot of pain and have cognitive issues. My eyesight is deteriorating alot. From -0.5 to 3.5+ My Nov MRI showed new lesions in brain and spine but my Dr says I should wait until July for next scan, that MS doesn't cause pain and that the seizures that I am experiencing are in my head. I don't feel anxious and don't bite the inside of my mouth or wet myself for attention. I don't remember the episode s but my husband says it is after flashing lights either on tv or Sun shining through leave less trees as we were driving past. .
Thanks for covering this important topic. As someone who has MS, I have found diet and lifestyle so important and so empowering - rather than letting MS control me, I can be proactive and make choices that benefit my general health and positively impact the course of my disease. I’m glad that you made it clear that there is no one diet works for all - I believe that you need to find one that you can stick to, that fits in with your lifestyle and which gives positive results for you. For example, I know that OMS works for many, but in the end it wasn’t the right fit for me and I have switched to Wahls Protocol which seems to work much better.
Having this disease myself you do not look too bad when starting your treatment. One question it begs is was it worth all that ( I did see a central line fitted ) and how are you now...
Hi. Please, let us pray together. Dear God who art in heaven hallow be thy name thy kingdom come thy will be done on earth as it is in heaven, give us this day our daily bread and forgive us our trespasses as we forgive those who trespass against us and lead us not into temptation but deliver us from evil for thine is the kingdom and the power and the glory forever in Jesus Christ's name we pray amen.
Follow ups are generally done every 6 months with your treating neurologist via MRI. Straight after the treatments it's recommended getting bloods done by a hematologist, in your own country once your fly home from treatment. My wife is 4 yrs stable.
Do you happen to have any data or suggestions on which jab a RRMS patient should have if they are on plegridy injections? I'm in Victoria, Australia and the chief health officer has mandated everyone must be jabbed or we are not allowed to go to work onsite anymore. It's been so hard for me to finally get to a place where I am finally working and happy and probably on the healthier side of life that I've felt in years. I haven't really been sick for years and have been wondering if the plegridy has somehow helped make me super immune to colds and flu all this time.. but now the jabs are mandatory and I'm dead against disrupting or modifying anything that could be immune system "activating" like what I read these spike protein generating jabs are. I'm so stressed out i dont know what to do or which poison to choose if my only options are vaxivera (AZ), Comirnaty (pfizer) or spikevax (moderna) 😔. I don't want any of these anywhere near me to be honest. But our regulators (ATAGI here I think?) have stitched up our guidelines and made it impossible for pretty much anyone to get an exemption unless you are allergic to an ingredient in all 3 jabs. I'm forced now to either get the sack and stay home or be forced to get a jab I really don't want and have no idea how it will react with my medicine short or long term or how my immune system will react to more toxins in my body and start manufacturing spike proteins. It sounds quite dangerous to me really and I'm terrified. Please do you have any advice or will you be doing a video about the jabs and different medicines by any chance?
I have been asked to go on siponimod I have lower back pain and tight calf muscles which dosent help when walking would siponimod help with this I’m from South Yorkshire
