- 20
- 14 607
Lucie Petrelis
Switzerland
Приєднався 7 тра 2013
Join my journey of living with Multiple Sclerosis, and ADHD, while being part of the LGBT+ community!
I wholeheartedly share my experiences with the goal for you to never feel alone and find sustainable solutions to feel better.
I want to inspire you to perceive your reality differently and bring you new ideas and tools to enjoy your every day and to live your life in a way that makes sense to you.
I identify as a human, a patient, and a life coach.
My approach to life is outside the box.
I believe that we can achieve everything we want by doing it OUR WAY and following our authentic voice.
As a certified coach, I would love to support anyone who needs my help.
Disclaimer: I am not a medical professional. All my views and recommendations are based on my own experiences and on the experiences of my clients and guests. Any topic relevant to medication and treatment must always be aligned with the doctor who is responsible for your care.
I am open to collaborations!
I wholeheartedly share my experiences with the goal for you to never feel alone and find sustainable solutions to feel better.
I want to inspire you to perceive your reality differently and bring you new ideas and tools to enjoy your every day and to live your life in a way that makes sense to you.
I identify as a human, a patient, and a life coach.
My approach to life is outside the box.
I believe that we can achieve everything we want by doing it OUR WAY and following our authentic voice.
As a certified coach, I would love to support anyone who needs my help.
Disclaimer: I am not a medical professional. All my views and recommendations are based on my own experiences and on the experiences of my clients and guests. Any topic relevant to medication and treatment must always be aligned with the doctor who is responsible for your care.
I am open to collaborations!
Inattentive ADHD BEST TIPS & STRATEGIES (Episode clip)
WATCH FULL EPISODE: ua-cam.com/video/c6gsRZvy6rs/v-deo.html
For more ADHD content SUBSCRIBE to my channel and don't miss any new episode of Endless Opportunities podcast, life with MS and ADHD!
Do you or someone you care about need support making the best out of their ADHD life?
luciepetrelis.com
contact@luciepetrelis.com
For more ADHD content SUBSCRIBE to my channel and don't miss any new episode of Endless Opportunities podcast, life with MS and ADHD!
Do you or someone you care about need support making the best out of their ADHD life?
luciepetrelis.com
contact@luciepetrelis.com
Переглядів: 65
Відео
Inattentive ADHD REAL LIFE SCENARIOS (Episode clip)
Переглядів 222 місяці тому
WATCH FULL EPISODE: ua-cam.com/video/c6gsRZvy6rs/v-deo.html For more ADHD content SUBSCRIBE to my channel and don't miss any new episode of Endless Opportunities podcast, life with MS and ADHD! Do you or someone you care about need support making the best out of their ADHD life? luciepetrelis.com contact@luciepetrelis.com
Inattentive ADHD COMMON CHARACTERISTICS (Episode clip)
Переглядів 122 місяці тому
WATCH FULL EPISODE: ua-cam.com/video/c6gsRZvy6rs/v-deo.html For more ADHD content SUBSCRIBE to my channel and don't miss any new episode of Endless Opportunities podcast, life with MS and ADHD! @luciepetrelis Do you or someone you care about need support making the best out of their ADHD life? luciepetrelis.com contact@luciepetrelis.com
Understanding inattentive ADHD (Episode clip)
Переглядів 1662 місяці тому
WATCH FULL EPISODE: ua-cam.com/video/c6gsRZvy6rs/v-deo.html For more ADHD content SUBSCRIBE to my channel and don't miss any new episode of Endless Opportunities podcast, life with MS and ADHD! Do you or someone you care about need support making the best out of their ADHD life? luciepetrelis.com contact@luciepetrelis.com
Understanding Inattentive ADHD in adults and women
Переглядів 1883 місяці тому
In this brave new episode packed with truths and different perspectives, you will learn everything about inattentive ADHD, with practical insights and strategies that can make a real difference in someone’s daily life. 00:00 Introduction to the Podcast 01:59 Understanding Inattentive ADHD 05:49 Challenges Faced by Adults with ADHD 06:47 Inattentive ADHD in Women 09:10 Reasons for Misdiagnosis 1...
MS fatigue best strategies and mindset to transform your life
Переглядів 4184 місяці тому
😟 MS fatigue is one of the most debilitating symptoms of multiple sclerosis that is strongly impacting the quality of life of people living with MS. In today's video podcast episode, I share my most valuable insights and best strategies for handling MS fatigue and what to do about it. You will understand how this symptom shows up, how to minimize fatigue, how to prevent fatigue, and what should...
Life with MS and ADHD, How everything changed in 3 days
Переглядів 3935 місяців тому
🌟 Welcome to the very first episode of Endless Opportunities - Life with MS and ADHD video podcast! 🥳 This first story will blow your mind!!! 😆 I have been living with Multiple Sclerosis since the age of 22 and was diagnosed with ADHD at 42. For years I managed to cope with my symptoms and remain positive despite many physical, mental, and emotional challenges. I had growth in my self-developme...
3rd Annual SYMPTOM FREE - MS SUMMIT 2024 (Link below for your free registration)
Переглядів 1385 місяців тому
We are thrilled to invite you to the 3rd Annual Symptom Free MS Summit, a transformative online event featuring over 25 renowned experts in coaching, naturopathy, nutrition, herbalism, and more. Join us to learn: - How to reduce inflammation naturally - Mindset strategies for living powerfully with MS - Tips to regain mobility and improve quality of life - And much more! 🎁 Exclusive Offer: Atte...
My ADHD diagnosis over 40 transformed my life
Переглядів 1065 місяців тому
If you are an adult wondering if you have ADHD 🤔, step into my world as I share the moment everything changed over a simple lunch conversation about ADHD as an adult. From confusion to clarity, I share the journey of discovering my adult ADHD diagnosis and the profound impact it had on my life. Through raw honesty, I talk about the struggles and strengths that come with ADHD, shedding light on ...
Coaching for Multiple Sclerosis - This is what I do
Переглядів 1527 місяців тому
Small presentation of what to expect from my support as a coach for MS. I am a certified coach, and I have been living with Multiple Sclerosis since 2002. I have managed to overcome and handle many challenges and daily symptoms in a different way. My physical energy, mind clarity, and emotional stability keep growing. Today, I feel better than ever, and I am ready to support you or your loved o...
ALMOND-BANANA COOKIES (Vegan, gluten-free, lactose-free, no added sugar, high protein, easy-to-make)
Переглядів 5558 місяців тому
These cookies are an instant boost for MS fatigue and ADHD brain fog! I kept this recipe secret long enough, and now it’s time to share it. I have MS and ADHD, and one of my main challenges is fatigue and brain fog. And these cookies make me feel amazing while enjoying my coffee or tea for breakfast or during a break! If you, too, need something to boost your energy and keep you going, these co...
From despair to strength: My 22 years quest with MS medications
Переглядів 1,1 тис.10 місяців тому
MY PERSONAL EXPERIENCE and SIDE EFFECTS with treatments for Multiple Sclerosis: Cortisone, Mitoxantrone, Interferons Rebif and Avonex, Gilenya, and currently, Ocrevus. Please be fully aware that EACH MS PATIENT could respond differently to each treatment, and everyone’s experience is unique. In this video, you will hear stories about my MS treatments and witness through my experiential learning...
The concept of " COMING OUT" concerns us ALL and in ways that you never EVER thought about. 😳
Переглядів 13411 місяців тому
The concept of " COMING OUT" concerns us ALL and in ways that you never EVER thought about. 😳
Preparation before a medical treatment The case of Ocrevus for MS
Переглядів 143Рік тому
Preparation before a medical treatment The case of Ocrevus for MS
Ocrevus infusion full process and side effects - My personal experience
Переглядів 934Рік тому
Ocrevus infusion full process and side effects - My personal experience
Thank you for sharing- its a frightening journey but I live by 'Adapt and conquer' - little victories 🦋
@@mariankiely3995 Thank you for being here Marian! Your philosophy of living is actually very powerful ❤️
Was allergic to rebiff and copaxone
Thanks for the video!
Please see my video about MS anti oxidants and detoxification. I had many of the symptoms but they are all gone. Cheers
I totally understand. I feel a pang of sadness when I go for my 6-month dose, as it's a harsh reminder that I'm living with MS.
Hi Yenifer, yesterday I did my 6th Ocrevus infusion and this time my best friend was with me. We were chatting, eating (healthy food I had prepared in advance and brought in tuppers), and being together. The whole experience was so different!! I didn’t feel the time passing, I had no sadness and it was great ❤️ Maybe for you too having a real friend along could make a big difference. I send you all my best wishes wherever you are!
Have you tryed carnivore ?
@@imadragnZ I do eat meat. I eat a variety of all food.
I am in Canada and was just diagnosed in July. I had terrible experiences with the medical community. Over the course of 6 weeks, I went from normal neurology to basically unable to walk more than 20 feet at a time. My blood sugar levels and blood pressure were wildly fluctuating and they thought I may have strokes. I could barely control by bladder or my back end. My family doctor (great) sent me to emergency with a letter to see neurology immediately because I was having rapidly ascending paralysis symptoms and loss of sensation, and severe muscle weakness. The doctor in the hospital ignored the letter and sent me home when the paralysis and weakness was at my knees. He literally said "I don't think you'll stop breathing so you're good to go home". A whole neurology department was available to see me that day. I had a neurology test 2 weeks later and by then it was at my armpits with rapidly tightening of my chest making it hard to breathe. I was immediately admitted and then 5 days later had a 70 minute MRI of my brain and entire spinal cord. They found massive damage and lesions that they said were new and decades old and they couldn't believe I could walk at all. As a chronic pain patient and former high level athlete they were amazed I had never been diagnosed in my teens or 20s, because my body had been fighting it all that time until it just couldn't. It's been almost 2 months and I still haven't seen the MS clinic, so hopefully I get some treatment soon before too much more damage is done. Stay strong!!
I think I have MS.. Or my doctor suspects I have it. I’ve been in a lot of pain and exhausted but all blood tests are coming back ok. The doctor said that she wants me to see a neurologist next but she has not mentioned MS. Now, after watching people’s videos on their symptoms, my ones are matching almost 100%… the biggest scare was when I woke up one day and half of my face and chest was numb. I went to the cardiologist but all was ok. So a neurologist will be next…
Hi Kristine, a neurologist is a path that hopefully will get you to some answers you need. If this first neurologist doesn’t give you specific directions such as an MRI at least, and you are still hanging there without any specific steps, find another neurologist. You need someone you will feel trust and will truly hear you. I know that so many MS symptoms can be very scary such as the numbness you described. Don’t let it discourage you as it could become much much less strong in the next days or weeks. It can come, it can go. (You will stay!) Focus a lot on your nutrition and do your best to eat really good things that are as much as possible without processed foods and definitely without at all ultra processed foods that are increasing inflammation. Also mind the heat and the high temperatures as can make things much worste. Sleep as much as you need it to regenerate your body. And do simple things in your day that bring you joy which do not harm you! You need joy!! I send you much love and all my best wishes ❤️
MS is a parasitic sickness A parasitic cleanse is needed Doctors dis not learn about this GREAT AWAKENING!
Constant pain on left side of body neck shoulder,arm my left shoulder swollen an hurt an lower part of arm feel like someone punched me arm fingers go numb can't sleep on left side have to lay on back
WALKING UPHILL OK. NOTDOWNHILL!
GREAT❤.ITS NOT EASY! WALKING UPHILL IS OK😅😢 BUT FORGET DOWNHILL! VIV XX
THANKS.🎉. YOU R BRILL! VIV XX.
TĤANKS.!❤😂.
NEED 2 FIND A CURE! V1V X
Parasitic cleanse. Parasites in thé brain and organs Do your research
❤❤❤
🎉🎉🎉🎉🎉🎉🎉🎉🎉🎉🎉
@@amelianolan9708 🥰
Very nice podcast 🙂
@@aleshudek5323 Thank you so much! 🥰 Let me know if you have a specific topic in mind that you wish to see on a next episode.
@luciepetrelis Hi, I'm not sure what I want to see. I think you doing great job and visually looks good. I really annoying to watching and listening. I wish your channel more subscribers x 🙂
Did You gain Weight getting this Treatment.
Wow what a journey ❤️ I have been very stubborn after my diagnosis in 2008, to not accept the injections, as a regular treatment and went on with my life. Till, 2020 when my condition suddenly became worse, and I started on Tecfidera the following year. I also took Mavenclad and the side effects were worse then I ever imagined, and from last year I started Ocrevus. You doing really really well. Unfortunately my fatigued is crippling me, and also my head doesn’t feel good. But I’m positive. You amazing and never forget that ❤
@@aluna_m888 Thank you so much!! I am sure your journey must have had also many intense rollercoasters. I hope you will feel better soon!! Btw, I recently made a video on MS fatigue. In case it helps! Stay strong and stick around to share our journeys ❤️
Last time I was in the hospital more or less 9 hrs … such a long process but it’s twice a year so I have to accept it, and take it easy on the day.
@@aluna_m888 Exactly. Take it easy and find ways to support yourself on that day. ❤️ And do little things to give yourself joy, even during the process!
Thank you for sharing. I recommend checking Dr. Terry Wahls story and protocol. After 4 years in a wheelchair, she managed to get better and is now walking and riding a bike. She has received over 2 million dollars in funding for her MS research. Check it out here and online too. She has also written books about it. There are also doctors saying that some medicines to lower cholesterol are causing MS... Myelin is 70% fat and most of it is made of cholesterol. I reccomend Dr. Hannah Yoseph book on MS too. 😊
Thanks, my major difficulty is walking without fear of falling. Let me know if you have any solution for that. Thy again for wonderful video.
Interesting. I was allergic to rebiff and copaxone
@@ctjmaughs How did the allergy show up?
78, don't really have fatigue but have plenty of other symptoms. Dx 35+ yrs ppms.
Hi from Israel thanks for the wonderful description of fatigue God bless you
Thank you so much! 😊
I am thankful I came across your educational video! It's been 12 years, and still yet no answers. I have had MRIs in the past but have only shown degenerative disk & joint in lumbar & cervical since age 32. It was June/ July every year warm season begin and the same numbing, tingling, shocking, and pain on either left or right side. I have not been able to see well since 2011. Everything is blurry within arms length. I suffer from optical neuritis in my left eye., and I'm here because I'm trying to find answers. Last week, I explained all my symptoms to a nurse at the hospital doing my stress echo, and she suggested I see a neurologist because my symptoms and new ones present MS. My new symptom is the squeezing around my ribs. She was diagnosed 5 yrs ago, and she had the same as me and was diagnosed 5 doctors later. Be well Im glad I found your channel 😊
@@NurseMora Thank you so much for being here and sharing your story!! ❤️ Please don’t stop searching for answers and also try to test different things to see how your body is responding. For example, regarding food, without focusing strictly on what is healthy “in general”, try to see if some ingredients make things worse or better for you. For me what plays a MAJOR role negatively is ultra processed and many processed foods, all sugars (besides natural ones such as fruits and honey), alcohol, products with lactose, I would say gluten but then also non-gluten solutions impact me negatively, and more. Also not enough sleep makes things worse. Some stretching exercises make like electricity passing through my body the next day. My menstrual cycle impacts A LOT my symptoms. Also if I am upset or stressed everything goes bad. When it’s too hot, I under function in all levels. But when I know what is helping and what not, this information becomes amazing tools! So, be a detective of your body and see what impacts you positively and what negatively. Knowledge is very powerful!! (I will definitely make a video on this!! 😆)
thank you lucie!
@@spencer6459 My pleasure! Thank you for watching 😊
Thanking for a time-line
Hi Lucie. Greeting to you from New York..now 7/1/84. Well I am in late 70's, have ms too. For 35 years..ppms. Let's correspond. Good?
@@scores718 Hi Esther, feel free to write to me an email: contact@luciepetrelis.com
Hi Lucie. Ty will write to you thru website!!-esther
Many thanks for this
You are very welcome! 😊
Do you use or increase melatonin. I heard it helps REmyelination of myelin . Feel better,,,
Never tried but I will look into it! Thank you so much!
Thanks for sharing your story
You are very welcome. Thank you for being here!
I am looking forward to listening to more! 🎉
Thank you! Next episode coming soon!! 🤗
Madam iam from india i want online consultation please give reply madam
Hi Nithin. Please contact me @ExploringMS
Madam please help me i want online consultation please replay
Well done 😅
Thank you!
Hello. I’m trying to find someone who can help me find what I have. I thinking that I have MS because I have a lot or I can say all the symptoms of MS but because I have another rare disease that can help to have a Neoro disease they are losing time with the other disease. Can you tell me the name of the doctor of France?
Hi Filipa, I am so sorry you are dealing with many health issues at the same time and still searching for some answers. It's not an easy phase but please stay strong. Unfortunately I don't remember the name of the doctor as it was 22 years ago but the hospital was in Aix-en-Provence, France. If I find his name, I will write back to you - in case he is still in practice. In the mean time, please, take the best possible care of yourself, eat well, sleep well, stay away from too much heat. Stay out of sugar, processed foods, alcohol, because they cause inflammation to the body and this is our biggest enemy. Also, focus on the quality and quantity of your sleep. No matter the health condition(s) you have, reducing inflammation and giving your body what it needs could make a HUGE difference. I truly wish you all the best!
I have been symptom free since 2018 and that’s such a relief!
That's amazing.
That’s truly wonderful!! I am very happy for you 🥰
@@luciepetrelis thanks 🙏
Lucie you just described me! Me diagnosis are the other way around, adhd and now an autoimmune disease, most likely MS, all my autoantibodies came back abnormal now waiting for more results. Wow! Thank you
Dear Sam, thank you so much for your message!! I hope you found some warmth in knowing that you are not alone in all this. Do not hesitate to write to me if you have any specific topic in mind about life with neurodiversity and an autoimmune condition. I just started a video podcast called Endless Opportunities - Life with MS and ADHD (you will find it, here, in my UA-cam channel and on Spotify). I am looking for the most important topics so I can create awesome episodes and help people just like us! For your ideas: contatct@luciepetrelis.com I send you all my love and support, Lucie
@@luciepetrelis thank you so much, it’s definitely a strange place to navigate. I’ve had a day where physically I just can’t so I’ve given myself small tasks to do before I start my paid job(fortunately I work from home now). I appreciate your advice and perspective thank you for sharing x have a wonderful day
Well i can say everyone should respect and love each other. Even Jehovah god found in psalms 83:18 the almighy may not condon such lifestyle but he loves every one❤❤
The antihistamine is probably responsible for the sleepiness, not the ocrelizumab.
@@shaneminogue982 You are right. And I think also the process is bringing some exhaustion physically but also emotionally.
You have a very nice wisdom and energy. I have a new neurovascular autoimmune dissase and i am trying to get used to my self. I have neuropathy disautomia and burning feet and hands in particular but it is not the worst compared to other patients
Thank you so much for your message and wonderful words!! I used to have burning feet and now just sometimes. What has made a huge difference for me was the radical change of diet. In case you want to try: No sugar, processed, alcohol, most cheeses. I would say also no gluten but any gluten-free version is still a problem for me. So I just stopped eating any bread, wraps, pastry, pasta and stuff like that. Just in case, I have started a video podcast also in my UA-cam channel, here, and on Spotify. It's called Endless Opportunities - Life with MS and ADHD. I focus on life with neurodiversity and auto immune conditions. I wish you all the best and I hope you will stick around!
People stigmatized w/a Multiple Sclerosis Diagnosis need access to Vascular Treatment research. STUDIES show Science Confirmed Recognized Medical Condition CCSVI preludes UNPROVEN autoimmune THEORY so called Multiple Sclerosis. Eliminating cause of SymptoMS WILL End MS!
People stigmatized w/a Multiple Sclerosis Diagnosis need access to Vascular Treatment research. STUDIES show Science Confirmed Recognized Medical Condition CCSVI preludes UNPROVEN autoimmune THEORY so called Multiple Sclerosis. Eliminating cause of SymptoMS WILL End MS!
Supplying Oxygen and Nutrients to every Cell along with clearing toxic brain waste, what is the role of CCSVI Venous Hypertension and proper/improved Cerebrospinal flow, impacting neurological symptoms regulating mood and cognitive Senescene Psych issues? #CCSVI #BloodFlowMatters Supplying Oxygen and Nutrients to every Cell along with clearing toxic brain waste, what is the role of CCSVI Venous Hypertension and proper/improved Cerebrospinal flow, impacting neurological symptoms regulating mood and cognitive Senescene Psych issues? #CCSVI #BloodFlowMatters What is the role of proper/improved Blood flow supplying Oxygen and Nutrients to every Cell in a Body circulation has made yourself what you are functioning today! Nothing else matters fighting climate change! #CCSVI #visiblemedicalconditioncausativeMS What is the role of proper/improved Blood flow supplying Oxygen and Nutrients to every Cell in a Body circulation has made yourself what you are functioning today! Nothing else matters fighting climate change! #CCSVI #visiblemedicalconditioncausativeMS What's the connection between Coronavirus and ARDS? FB Group: MultipleStenosisSociety t.co/S5GPkckCfr 'Fluid leaks from small blood vessels and collects in tiny air sacs in your lungs so they can’t fill with enough air' #CCSVI #microbleedings Facilitate Research Cerebrospinal Venous Blood Flow Baseline Primary Care Option Treating Neurovascular Disease like Covid-19! Longevity Quality life depend! #What's the connection between Coronavirus and ARDS? FB Group: MultipleStenosisSociety t.co/S5GPkckCfr 'Fluid leaks from small blood vessels and collects in tiny air sacs in your lungs so they can’t fill with enough air' #CCSVI #microbleedings So happens CCSVI is a MINIMALLY INVASIVE TREATABLE Congenital Science Confirmed Recognized Medical Condition studies show causative factor so called Multiple Sclerosis and role/part 43 other so called Neurological Afflictions Including Migraines! SymptoMS often ease/disappear including fatigue, vision, bowel and headache in the CCSVI angioplasty group #Symptoms often ease/disappear! Facilitate Collaboration Neurovascular Disease Research! #CCSVI FB Group: MultipleStenosisSociety t.co/YYPIA4tRuM Courage for hope Sharing Research Cerebrospinal Blood Flow Treatment/s Baseline Primary Care Option Treating Neurovascular & SO CALLED AUTOIMMUNE DISEASE! Eliminating cause Multiple Sclerosis will End MS! Facebook group: t.co/GIyHzwBeTp If you had noticed #fatigue! An exciting new RCT shows improvements of Clinical Functional Measures in multiple sclerosis following PTA. Despite the little sample fatigue, urinary urgency, headache, cognition are significantly better in the PTA arm. FB Group: MultipleStenosisSociety m.facebook.com/groups/493935520792751/permalink/1547908968728729/ Science confirmedcausative factors for Neurovascular Diseases Multiple Sclerosis and Covid 19 involve Chronic Cerebrospinal Venous Insufficiency (CCSVI) yet to be fully understood genetics and environmental issues such as infections or food/vitamin nourishment! Science confirmed causative factors for Neurovascular Diseases Multiple Sclerosis and Covid 19 involve Chronic Cerebrospinal Venous Insufficiency (CCSVI) yet to be fully understood genetics and environmental issues such as infections or food/vitamin nourishment! What's the connection between Coronavirus and ARDS? FB Group: MultipleStenosisSociety m.facebook.com/groups/493935520792751?view=permalink&id=1372288126290815 'Fluid leaks from small blood vessels and collects in tiny air sacs in your lungs so they can’t fill with enough air' #CCSVI #microbleedings #BloodFlowMatters What's the connection between Coronavirus and ARDS? FB Group: MultipleStenosisSociety m.facebook.com/groups/493935520792751?view=permalink&id=1372288126290815 'Fluid leaks from small blood vessels and collects in tiny air sacs in your lungs so they can’t fill with enough air' #microbleedings #BloodFlowMatters So happens CCSVI is a MINIMALLY INVASIVE TREATABLE Congenital Science Confirmed Recognized Medical Condition studies show causative factor so called Multiple Sclerosis and role/part 43 other so called Neurological Afflictions Including Migraines, Asperger Autism, Dementia/Alzheimer's, Aphasia, Optic Neuritis, Tinnitus, Transverse Myelitis, Parkinson's Disease, Lyme Disease, Meniers Syndrome, Ehlers-Danlos ect., Ect., ECT.! As much the unproven autoimmune theory so called MS is being referred to as a slow Stroke! #BloodFlowMatters Keep in mind! Supplying Oxygen and Nutrients to every Cell in a Body, Blood circulation, including activity/exercise. Building Blocks of life, having made yourself what you are functioning today! Nothing else matters! Science!!! FB Group: MultipleStenosisSociety facebook.com/groups/493935520792751/?ref=sharec Apparantly nothing else matters critical Healthcare research facilitate collaboration defining the path forward establishing the understanding and treatment of Neurovascular disease? organizing unified clarity in Science knowledge and progress! #CCSVI 'Fluid leaks from small blood vessels and collects in tiny air sacs in your lungs so they can’t fill with enough air' #microbleedings #BloodFlowMatters So happens CCSVI is a MINIMALLY INVASIVE TREATABLE Congenital Science Confirmed Recognized Medical Condition studies show causative factor so called Multiple Sclerosis and role/part 43 other so called Neurological Afflictions Including Migraines, Asperger Autism, Dementia/Alzheimer's, Aphasia, Optic Neuritis, Tinnitus, Transverse Myelitis, Parkinson's Disease, Lyme Disease, Meniers Syndrome, Ehlers-Danlos ect., Ect., ECT.! As much the unproven autoimmune theory so called MS is being referred to as a slow Stroke! #BloodFlowMatters Keep in mind! Supplying Oxygen and Nutrients to every Cell in a Body, Blood circulation, including activity/exercise. Building Blocks of life, having made yourself what you are functioning today! Nothing else matters! Science!!! FB Group: MultipleStenosisSociety facebook.com/groups/493935520792751/?ref=sharec Apparantly nothing else matters critical Healthcare research facilitate collaboration defining the path forward establishing the understanding and treatment of disease orgaizing unified clarity in Science knowledge and progress! #CCSVI
Loving your videos, just subscribed 😊 thanks so much for putting out your content!!
@@Roller.bex. Thank you for watching and sticking around for more!! 😊
Thanks for sharing your experience! “Not doubting yourself anymore”, omg, this can be sooo liberating!
It absolutely is!!! Thank you so much! 😊❤️
DR ALAHO OLU on UA-cam Channel you’re indeed a great and trusted traditional and holistic herbalist, he cured me and my wife from Multiple Sclerosis, he also has cure for HPV, HSV, HIV, FIBROID, ALS, CANCER, LUNGS DISEASES………
DR ALAHO OLU on UA-cam Channel you’re indeed a great and trusted traditional and holistic herbalist, he cured me and my wife from Multiple Sclerosis, he also has cure for HPV, HSV, HIV, FIBROID, ALS, CANCER, LUNGS DISEASES………
My first symptom happened when I was about 50. It felt like there was cell phone on vibrate in my foot. That was 15 years ago. Things have gotten progressively worse.
Stay strong, my dear Cynthia ❤️ I send you much love
@@luciepetrelis thanks so much
Same here for me. Got diagnosed around 50 and going down hill daily
@@sivanmahadevan2458 I am so sorry.. this disease is merciless