Blessings in an abundance of the faith. I salute you. 😘🙏Grace and peace be unto you and to this place. God bless you. 🤍🌈🤍Thank you. Will you believe and receive Jesus Christ as your LORD and personal saviour??? I do. 😊
It’s very hard to hear this important information with that annoying electronic noise in the background. You ruined your video and limited it’s effectiveness.
Who says Genital herpes virus has no cure and permanent treatment? Let me introduce you all to Dr IGUDIA on RU-vid who cured my partner and I friend Genital Herpes infection with his natural herbal medication.
I'm 37 and had an MRI that showed 5 quite small non specific t2 Hyperintense foci. My neurologist said they're quite normal with aging and wasn't too concerned. Should I get a second opinion?
Same here and my neurologist didn’t even call me back ! I still have an EMG and a nerve conduction test pending but my rheumatologist called me yesterday and advised me to look for another neurologist 😐
@@SarahCSarah Keep me updated, I had all those tests done and all seems well. I guess there's not much we can do about it except maybe get an mri each year and monitor for changed. :) Good luck Lola
Thank you very much for this. I have a brain/cervical spine contrast MRI scan this week (to explore potential MS diagnosis). This is really helpful and clear so I can ask the right questions about the results at my follow up.
Does anyone know about T2 flair foci? Thats what my report says. Not T2 flair lesions but T2 flair hiperintense foci. I just have follow up appt. until another 3 weeks and is too far from today.
@@TheAjsquaredaway neurologist said those are just spots that i could have gotten due to migraines but im getting a second opinion on nov 2nd. from a ms specialist from Ohio
@@TheAjsquaredaway update: got a second opinion from doctor Aaron Boster in Ohio and thankgod he didnt rule it out as MS. I do have some spots but not consistent with MS. I dont know what I have now. Could be fibromyialgia. 🤔
@@edo8797 non prendo più tysabri da diversi mesi, ho dovuto interrompere per improvvisa ed elevata positività al virus JC, sono passato ad Ocrevus. Entrambi i farmaci non mi hanno mai dato problemi e non ho avuto ricadute dal 2017 (anno in cui avevo iniziato tysabri)
I have just left hospital after 2.5 months learning to walk and talk again . I was told nothing was in the scan so it can’t be ms . However I was discharged and saw it says “ left lobe t2 hyper sensitivies ‘ isn’t that the area to do with walking and talking . I have met with m s society who said 40% don’t have lesions show on mri if they are microscopic .yet the symptoms are still there . They also said 10% don’t show wirh spinal tap and mri . I was instead told I have FND . However I know this is often misdiagnosed when it’s ms esp if you have functional symptoms as a result of the m s symptoms. Would you suggest I get further testing / second opinion ? I am very fit , super healthy to a fault , don’t drink or smoke or take any medications .
Big useseless gangbang drug. Studies not worth for its, its useless garbage, outdated und totally fails in every aspect of life. The youth isnt willing to take it the usecase is very limited and the side effects are too much.
Lovely Video clip! Apologies for chiming in, I would love your thoughts. Have you heard the talk about - Liyaraah Sclerosis Redemption (probably on Google)? It is an awesome exclusive product for overcoming the symptoms of multiple sclerosis minus the hard work. Ive heard some decent things about it and my work buddy after a lifetime of fighting got cool success with it.
This is interesting and I know there's still ongoing studies of the "whys". I researched online for Dorsal Pons lesions but couldn't find anything, glad I researched on here and stumbled on your teachings. I've been researching extensively for 3 year's trying to get to root cause of my 24/7 floating like feeling in my head, it's persistent, always there, tingling both feet for 3 year's, more dominate in right foot, chronic fatigue, Tinnitus that began this August 2020. I've had a series of tests conducted by a Neurologist, Cardiologist and Audiologist, had extensive tests blood tests, CBC, ANA and extensive antibody tests, Vitamin B12 and D which that one was low at 26 and began a supplement 2 months ago. Had a full thyroid panel done, TSH/T3 & T4 and my TSH had moved to hyper being 26 and since had dosage of thyroid meds decreased, was diagnosed with Hypothyroidism in 1993 and had half the gland removed but in all the year's never experienced these symptoms. In 1993 had a "full" hysterectomy, was placed on HRT- Estrogen and than in 2017 had to hault the HRT and that's when I noticed these symptoms began. I'm a 54 year old female. I'd seen a Neurologist, about 3 vestibular tests and nerve functioning test were conducted in addition to a MRI in which 2 small white matter lesions were found. *Note- I didn't use contrast as I'm allergic to it. *All vestibular tests were normal*. *First one: Frontal subcortical lesion of left superior frontal gyrus, ( measurement not noted). *Second one: Its termed as a "vascular variant", located in the "Dorsal Pons", it states "may" be a ,"vascular variant", my understanding it could had been at one time I had a small (TIA) there's no certainty to that though. The measurement is 0.2 × 2.3. CM. (Seen on a T2 Flair). Noted*- I didn't have the dye for the MRI as I'm allergic to it. However apparently my symptoms are not associated with the lesions. "No demyeliative plaques identified that would call for MS- Multiple Sclerosis". From the research I've done in trying to understand these findings, what medical language is, where these regions are in the brain, in my understanding is the Dorsal Pons is located in or near the "brain stem", so I'm wondering if a lesion in that particular place or in frontal lobe can cause any sort of vestibular disorders. My understanding also is if brainstem is effected that can cause serious issues so therefore wondering since Dorsal Pons is in the brainstem or a part of it if that could present vestibular disorder. This is all so overwhelming for me trying to learn this but am trying. After all there's still ongoing studies, still learning so wondering if a possibility. I'll be hopefully returning to my Neurologist sometime soon for a followup as I had switched health insurance coverage so couldn't see him, my regular doctor whom is very kind and caring recently forwarded my 2018 Nuerology report to her fellow colleague Neurologist to get their opinion and they didn't see anything alarming, stating the vascular variant could be from something I was born with. Still wondering if possibility of MS. Any suggestions and guidance you may have I would be very grateful. I thank you Doctor and all of you from the bottom of my heart in the medical field for all that you do, greatly appreciated.
@Truth Teller, Same story as you even diagnosed with Thyroid Storms, Graves. Same same same. It’s scary. I’ve been since 1990, told it was all in my head. They didn’t know how tight they were. I think we have to start changing the narrative with the Medical System. Xo
@@lisamarie6411 Thank you much for sharing, truly appreciate that. I'm so sorry you've experienced similar, it sure is complex. When things of this nature happen, it gets frustrating when some in the field of medicine are "too quick" to dismiss it as mental health related. I understand that can be the cases at times, but before every avenue is exhausted, they shouldn't readily dismiss and place it under the mental health umbrella. Thyroid alone can cause a patient to manifest mental health, as you know in the case of moving to hyperthyroidism how the anxiety can be horrific. More doctors need to start listening to patients, they're human beings too therefore don't have all the answers all the time, in addition, medical field is always evolving. Doctors can learn from patients just the same as patients learn from doctors. I have great appreciation and respect for doctors, just would like more to come on board to building a better relationship with their patients and really listening, and be open to suggestions. I agree with you, time to begin changing the narrative in the medical system. ❤
After my Multiple Sclerosis diagnosis 2 years ago, i stopped all the Multiple sclerosis medicines prescribed due to severe side effects, and decided to go on natural herbal approach. My primary care provider introduced me to Dr Oduwa and i immediately started on their Multiple Sclerosis herbal formula treatment, this herbal treatment has made a tremendous difference for me. My symptoms including shaking, muscle weakness, fatigue, mood swings, numbness, double vision and urinary retention all disappeared after the 4 months treatment! contact Dr Oduwa the herbal healer at { info@droduwaherbalhome. com } you can visit his website at droduwaherbalhome.com/ or you can whatsApp him at +23481363534191
My daughter is just 18 years of age and was discovered with this condition at the age of 15 when she developed problems with her eyesight. We were devastated as a family as most members of the family work in the NHS as clinicians/practitioners and educators. She was psychologically broken down. Although she is coping and managing herself now and doing well in her A levels and starting her university in September. The fear is that she will be far away for us to keep an eye on all her ailments that need to be dealt with spot on.Thank God for everything for finally directing us to Dr. Stella who gave us her natural herbs and told us how to use and after three months, my daughter is ok and free totally forever, Contact Dr E-Mail -doctorstellaidemudia@gmail.com and doctorstellaidemudia@yahoo.com WhatsApp - +2348157471852.
My daughter is just 18 years of age and was discovered with this condition at the age of 15 when she developed problems with her eyesight. We were devastated as a family as most members of the family work in the NHS as clinicians/practitioners and educators. She was psychologically broken down. Although she is coping and managing herself now and doing well in her A levels and starting her university in September. The fear is that she will be far away for us to keep an eye on all her ailments that need to be dealt with spot on.Thank God for everything for finally directing us to Dr. Stella who gave us her natural herbs and told us how to use and after three months, my daughter is ok and free totally forever, Contact Dr E-Mail -doctorstellaidemudia@gmail.com and doctorstellaidemudia@yahoo.com WhatsApp - +2348157471852.
@@cherry2619 sorry for the late response. i used to have symptoms,my right hand went numb all of a sudden,that was the reason that i went and had a scan. but after i was actually diagnosed they offered treatment that was effective thankfully. now im all good thanks to the medication im taking. no symptoms whatsoever. best of luck to you and despite the results,don’t forget to keep your head up
@@ketamukhraneli9268 im so happy to hear you're doing better, it gives me hope too. the only symptoms i ever had was some occasional burning in my thighs, but they never lasted more than 24 hours continuously and my doctors keep saying the symptom has to persist for 24 hours before it is considered a possible MS symptom
@@cherry2619 i hope its nothing serious. i had the numbness for like a week straight,to the point that i couldn’t even sleep at night. everythings treatable so don’t be scared.
@Practical 100% i'm no specialist or anything, but if you notice that the leg tightness leaves every time you eat or drink something, then i wouldn't think it's a symptom of MS at all, because the MS symptom should be there regardless of whether you're eating or not. I do know that many physicians say that a symptom of MS should last at least 24 hours, so if yours doesn't then that might also be an indication that it's not MS. In either case, see a doctor because I'm not a specialist but I don't think you should be afraid.
Hey, i feel numbness, tingling and random pains all over my body, butt,face,legs,back,belly,arms,hands, feet..but my all exams including the mri are clear and inconclusive. What do I have then? Idk it just keeps getting worst and no one knows how to help me plz i would appreciate any advice.
Have you have your vitamin levels checked with a blood test? B12, iron and D3 deficiencies produce very similar symptoms. Also maybe ask for a referral to a rheumatologist and get them to check for your ANA levels (which will show if you have any kind of inflammatory conditions like lupus, etc.).
My MS symptoms were actually caused by Mercury toxicity. In 1999, after having two silver fillings drilled out, I immediately suffered from killer headaches, skin tingling, vision problems, foot-leg-body numbness, fatigue and other neurological and mobility problems. Today, I am fully cured and remain 100% symptom free. Praise God! - Debra [www.hopeandhealingbook.com]
The music and voice really makes it less or it's not so bad everything will be alright follow Doctor's orders go over your MRI with him and it will give you a better understanding what is going on with this MS.... I did.
