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While you got paid unemployment and forgivable loans for your business….

I've had mutiples scerisos

You will get lots of utis

Not everyone who has ms has someone to fall back on. Once your sick it seems people slowly disappear

Yes it is exhausting having to explain all the details again and again

Off topic - and thank you for your videos- you are Heather MacDonald’s dopleganger! #juicyscoop :)

I've had it for 16 years my I told all my friends and family that I had it

I hope you are ok. I will tell you after implants for 20 yrs, I had them removed as my symptoms were getting worse. Some got better but that is one thing I think of, did these implants make me sick. I’m not MS diagnosed yet, have 1 yr follow up end of this month with neurologist. Vision issues very scary. I work as an office manager and nursed pt for 5 yrs, ran myself ragged so I can relate to your feelings of ‘I did this’. Single mom too…..scary thinking about being alone or having to rely on people for help. I left second job with hopes of relaxing more, menopause certainly sucks and doesn’t help but hang in there. I’ve never appreciated the ability to move and see more than now. I try very hard to meditate and enjoy the little thing. I really do hope you are doing well on your meds. To everyone below, I wish you all the best.

I’m new to your channel and have watched all of your videos. It helps me to hear about your experience with Ocrevus. I was diagnosed in February 2023. After 3 different neurologists I’m finally starting a DMT. Hope you are well. Can’t wait for your next video. God bless. ((Hugs))

Just watched your first video, skipped to this video. Glad to see you are doing well. I’m experiencing weird things: Numbness, Tingling Pins and needle, Itching and Electric shocks and major fatigue which led me down the MS rabbit hole. I have an apt in 2 weeks with the neurologist. I’m so scared lol. I’m a healthy 45 year old male, in the gym daily, always healthy, and suddenly my world has been flipped upside down. Doesn’t make it any better that I’m single now for the first time and now, the stress and fear of “not finding anyone that would want to to be with me if I have ms ” is replaying in my mind and legit taking me out emotionally. Like you said in your first video, feeling alone and scared is where I’m at. I’m hoping you can make more videos so we can keep up on your journey.

Hi.How are you? I would like to ask you if ten years before you had depression and stress

Hi Ashley, I have RRMS as well. I was diagnosed in January of 2023. I have been on Kesimpta and it has been working well for me. I had double vision for 7 months roughly and had to get surgery to correct it. If and when you get the live chat figured out you should let all of us know.

Get a homeopath

You give light at the end of the tunnel for myself. Was diagnosed two days ago and waiting to see if insurance will cover Ocrevus or if I have to do another drug. Thanks for sharing

Would love to have more connections to know life goes with this. Was just confirmed yesterday that I for sure have multiple sclerosis. Lost my sight in the right eye and never realized my walking uses had a name. I never knew what for drop was until now. Just thought I was super clumsy. So glad you post about your issues.

Just confirmed yesterday that I have ms. I’m not for sure if I want to tell anyone yet.

ultiple sclerosis for almost 10 years, it seems to me that simple exercises slow down its development, I am an example of this obvious. This is why the channel on RUclips started htps ://youtube.com/@ R-skl? si = P8tAJaob-e6uyaeW

What is the role of CCSVI Venous Hypertension and proper/improved Cerebrospinal Blood flow?? #CCSVI #BloodFlowMatters CCSVI is definitely one of the causes of MS. The novelty for some years is that we are certain that, after studying at the La Sapienza University of Rome, there are 3 types of CCSVI: * a 1 type with patients suffering from an obstacle to the endovacular venous discharge, i.e. due to congenital or acquired anomalies that restrict and block the drainage of the investigated veins (jugular, vertebral, azygos) * a 2nd type with patients suffering from an extra-vascular venous obstruction, i.e. due to external compression of the vessel * a 3 type with patients suffering from endo-vacular and extra-vascular venous obstruction So to simplify we can say that there is a CCSVI of the "hydraulic" type (1 type), a CCSVI of the "mechanical" type (2 type) and a "mixed" CCSVI of the two previous types (3 type), the 2 and the 3 type represent about 85% of cases. A patient with type 1 CCSVI will have a greater indication for angioplasty treatment, a patient with type 2 CCSVI will have a specific indication for specific physiotherapy decompressive treatment (RIMA Method), a patient with type 3 CCSVI it will have an indication for both an endo-vascular dilatation treatment and an extra-vascular decompression treatment. The RIMA Method devised by Dr. Domenico Ricci of Bari is able to release compressed veins throughout their course, as shown by a publication of June 2015 after a one-year study (Internal jugular Venous Compressione Syndrome: hemodynamic outcomes after cervical vertebral decompression manipulations-Pubmed). For information: Dr. Domenico Ricci cell.3393828399 MRI IN MS VASCULAR PATHOLOGY www.dropbox.com/s/m0yvgmufgfcys1v/MRI%20IN%20MS%20-%20VASCULAR%20PATHOLOGY%20.pdf?dl=0 This quantification of the disease pathology will help! #CCSVI Venous Hypertension >microbleedings >iron >inflammation >free radicals >neurodegeneration #multiplesclerosis M.S. - Mystery Solved Mysterious Autoimmunity = CCSVI Neurodegeneration M.S. - Mystery Solved Mysterious Autoimmunity = CCSVI Neurodegeneration Keep in mind! Also venous hypertension ➡️ impaired CSF absorption ➡️ reduced G Lymphatic drainage ➡️ interstitial peptides accumulation ➡️ NEURO INFLAMMATION #CCSVI Eliminating cause of the Symptoms of so called Multiple Sclerosis will End MS. Apparently it is unquantifiable the length of time Symptom$ can be treated! If you hadn't noticed Who Knew?? #BloodFlowMatters What is the role of proper/improved Blood flow? #CCSVI Apparently #BloodFlowMatters Stroke common occurrence in Individuals diagnosed with Diabetes, unproven autoimmune THEORY so called MS Supplying Oxygen and Nutrients to Cell in a Body. Blood Circulation through and including activity/exercise. Building Blocks of life, having made yourself what you are functioning today! #CCSVI #Healthcare game changer when the cause The doctor of the future will give no medicine, but will interest his patient in the care of the human frame, in diet and in the cause and prevention of disease. -THOMAS EDISON Best possiblity easing/eliminating cause of SymptoMS! You can relate! If your veins are blocked they should be opened if you have SymptoMS or not! MRI IN MS VASCULAR PATHOLOGY www.dropbox.com/s/m0yvgmufgfcys1v/MRI%20IN%20MS%20-%20VASCULAR%20PATHOLOGY%20.pdf?dl=0 Who Knew?? #BloodFlowMatters What is the role of proper/improved Blood flow? #CCSVI Apparently #BloodFlowMatters Stroke is a common occurrence in Individuals diagnosed with Diabetes Neurovascular Disease Multiple Sclerosis is being referred 'slow Stroke'. What is the role of proper/improved Blood flow in both conditions as much CCSVI has been Scientifically confirmed a causative factor in Symptoms of so called MS! Supplying Oxygen and Nutrients to every Cell in a Body. Blood Circulation through and including activity/exercise. Building Blocks of life, having made yourself what you are functioning today! #CCSVI #Healthcare game changer when the cause of the Symptoms of Medical conditions are eliminated! The doctor of the future will give no medicine, but will interest his patient in the care of the human frame, in diet and in the cause and prevention of disease. -THOMAS EDISON Best possiblity easing/eliminating cause of SymptoMS! You can relate! If your veins are blocked they should be opened if you have SymptoMS or not! A Vascular problem led to the crippling nightmare of Multiple Sclerosis The real Multiple Sclerosis nightmare started at the point of NeuroDx The disaster of diagnosis being made by general physical observation over time,. Especially when Time is something you can’t afford #CCSVI Multiple Sclerosis is strong and you often need help. Make you be worthy of this help, don't stand in a corner complaining, do your part! 💪 #Symptoms often ease/DISAPPEAR Facilitate Collaboration Neurovascular Disease Research! #CCSVI FB Group: MSS facebook.com/groups/4939355…!

Meditate and Diet. That’s all

Thank you for posting! I have a hard time with taking a shower especially if I have to wash my hair. It totally wipes me out. I only do makeup now then I go somewhere which doesn’t happen very much. I used to be so active, totally into bodybuilding, on my feet all day and enjoying it.

I am on ocrevus also but with no bad side effects. Thank god.

How long did it take for numbness to go away I have numbness for 6 weeks now I am scared that it will never go away I have rrms also ❤

I do want ask, the more ocrevus infusions you have? Do you feel better? I'm on ocrevus as well

Thank you for posting your videos and giving others who don't have multiple sclerosis a little understanding of this disease. I was diagnosed December 2022

Appreciate you being so open and sharing your story❤ My mom was Type A (as I am) and it was devastating to her when she began to deal with MS. You aren’t alone. I’ve often wondered if “she brought it on herself” too as you said. And I worry I will too. Love your honestly when you met your eventual hubby- glad you have a wonderful support system. Thanks again for sharing and explaining. Sounds like a blessing you were so close to the Mayo Clinic to get diagnosed in such a short time from that major debilitating episode!! There is no shame in taking meds- they may add quality and quantity of life if they slow the disease down. My mother wasn’t listened too and believed enough to get that option. By the time we realized what it was, she was already becoming disabled by it. Stay positive! Mind over matter❤

Thanks for making these videos! Ive been researching the genetic predisposition/ autoimmune/epstein barr/chronic stress component with MS. I was diagnosed with PTSD in 2018 and now just had optic neuritis (chronic fatigue and pain for 10 years) and in the process of MS diagnosis. Brain MRI not many lesions but 14 oligiclonal bands. Anyway, you mentioned having personality change a little bit with being short with people. I feel the same way! I think its just a mixture of being misunderstood with PTSD and not from the military and having chronic pain plus my optic nerve damage has myelin degeneration so I think we can have less patience from a structural standpoint because of this. Its not our fault! 🕊

I just finished my Florida real estate course when my symptoms started! Had to move to TN to live with my retired parents! Ha! But the market here is booming so I might get my Tn license! You go girl! I’m so proud of you 🙏🏻 You’re such an inspiration to all

Thank you so much for this video. I’m undiagnosed but I have an uncle and a great uncle that have MS and I’m concerned due to tingling/numbness in my feet. Can’t thank you enough for sharing about being afraid of what your now husband would think. I can’t even get myself to date because I’m 29 and feel like I’m broken. I cried listening to that, happy tears. You gave me hope I can’t thank you enough. I used to live in Melbourne and Fort Myers I miss Florida so much. I hope you’re well❤️

Well said

I was diagnosed July 23rd 2023 so I'm new to all this MS stuff. Come to find out through my MRI that apparently I've had MS for the last 7 years. My neurologist recommended Ocrevus right away so I started that in October and I go for my second infusion in April. My life has completely changed since being diagnosed. It's tough but I'm still walking even if I can't cook anymore... Hopefully that changes

Hi Ashley, congratulations on your new career. Looking forward to hear more about your journey

I don't know how i came upon your channel, but im glad. I know this video is 3 years old, but im wondering how you are now. I hope you are well! Thank you for sharing

Hi Ashley Im on Ocrevus as well. I got diagnosed in aug 2021 and i have rrms. I had a major relapse in oct 22 . I work out daily and my balance and everything is ok. The one thi k that depresses me is that my speech was affected. I think thats what depresses me the most. I can tell right now that im in need of my 6 month infusion and my balance i feel a little awkward internally if that makes sense. Im still able to drive etc other than the talking i feel great. In the beginning my speech improved but lately its gotten worse. I hope that my infusion which is due in another week will improve the spasicity in my voice . I know i hear that it does in your walking in which it does

Have you heard of paleomedicina and Dr zsophia Clemens they specialise in cancer and autoimmune diseases they have a clinic in Hungary but they have an online service as well they treat people with a metabolic approach diet only they have treated 7000 patients with a high level of success good luck

Don't feel silly. Ever! So great that you were able to change careers. Congrats on the home and the dogs 🐾 🐾

I’m glad you are back and are doing ok

I was just diagnosed with Ms. on October 8th, 2023. a couple of days before this, I was at work and felt drunk while walking down the hall the night I went to the emergency room I drove home a 20 min drive at the most took me 60 mins pulled Into the driveway parked my car opened my door to climb out and fell got up with my husband's help and fell again down the stairs he looked at me and said I needed to go in and I agreed thinking I had a stroke

I have gone through lot of the things you mention here. Luckily I was already married with 3 kids when I was diagnosed or I don't know if I would have had all of them. The unknown is scary, but ignorance truly is bliss! My dad tells me the reason I'm so tired all the time is because I don't do any hard work to tire myself out and get a good night's sleep. My aunt tells me I could do this job, that job, she has lots of job ideas for me. If it wasn't for MS, I'd be a high school English teacher, something I worked my butt off getting twenty years after graduating HS, but my first symptoms showed up while student teaching, and I wasn't diagnosed for 1.5 years later. Another relative told me I needed to use my brain more because the brain is a muscle. When I told her, no... She insisted it was. Unfortunately my brain muscle has too many lesions to work properly because I don't do enough hard work, I guess! Sorry to vent. Thanks for sharing your experiences. Ive been taking Rebif injections 3x weekly and have had no new symptoms or changes on MRI for 8 years, but still have vertigo, balance issues, cognitive issues, extreme fatigue, etc, etc. 😇

Hey Ashley I have RRMS too for about 2 years now been on the O for about a year in a half! So far so good but this disease is definitely a pain in the ass mentally and physically! Always looking to connect with more people who go though this! It can feel extremely frustrating and isolating at times but you’re not alone, maybe we can make some kind of MS group chat or something? Anyway just found your channel and wanted you to know I appreciate your videos and updates always here for support, we’re all in this together!

I started ocravus too, getting the second round of the first dose soon. I was curious to know if you have a specific diet! Thank you 🙏

Visiting Palm Springs, from Seattle. Need to absorb some sun ☀️

Merry Christmas !!

Hi I'm also on ocrovis

Thank you for your videos. Best from Franziska from Germany

Hi Ashley, I watched a couple of your videos, I just scroll through utube looking for people talking about ms symptoms, trying to find answers. My doctor says I have fibromyalgia but I'm not sure. So I search. Glad you are back

How are you doing?

I did ocrevus fir a year 2020 to 2021 now i am off side effects to many

So question did you get sick prior to your dx since it was covid year. I was dx same year

Granted I only had like two doses but I loved ocrevus. I take public transportation and have a baby in daycare and didn’t get more sick I don’t think. Sadly I had to stop because I became neutrophic, which is super rare. I also didn’t sick ever before I got diagnosed. I even told my husband I was a pinnacle of health lol probably should have been my first sign since my immune system was too good.

Go Vegan