How I discovered my Multiple Sclerosis
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- Опубліковано 29 вер 2024
- Yes, I’m advenced
I meant to say through exercise not medicine
#ms #multiplesclerosisfighter #multiplesclerosissociety #multiplesclerosiswarrior #multiplesclerosis #multiplesclerosisawareness #inspiration #notalone #weakness #excercise #workout
Thank you for sharing your story. I pray that God will help you get through this ms. It's not fun having to deal with physical ailments. It's good that you reach out by sharing your stories. You're not alone. It may seem that way, but keep plugging in and sharing. ❤❤❤
It’s not fun 😄 i feel it a more mental battle than a physical one. Once the mind gets weak, the body follows. I want people not to feel alone ❤️ the mind has so much more to do with illnesses, more than many know. The state of mind is important in any battle.
I am so sorry that you are dealing with what you’re dealing with. It’s OK to feel those emotions because having MS as long as I have had it, I have learned that MS is an illness that has many different stages of grief. You grieve what you was able to do you grieve what once was easy for you, but along with that grief comes immense strength. You have that strength in your weakest moments you will continue to fight your hardest battles and with God‘s glory everything and anything is possible.
Amen 😊 it’s harder for me to accept because of other stuff happening. It’s not a normal progression 😭 it’s hard not being able to talk 😑 i wont let this beat me 😊 although there are moments where i want to give into this horrific disease. It’s a mind battle more than anything 🤣
You're one brave lady.. your testimony brought 😢to my eyes..
God will get you through the bad and good times..
Please keep contact..
HUGZZZ
@@jennidix-peekwaters thank you 😊 yes He will and I am so thankful He gifted people to write lyrics because lyrics give me a push ❤️I will always be here ❤️
Thank you for your quick reply.
I live in Port Elizabeth in South Africa.
Off to sleep here now.
I have not been diagnosed, but I have all the symptoms..
Seeing a specialist on 05.12.2023..
We will pray for each other.
HUGZZZ
@@jennidix-peekwaters i try to reply when i see messages but it won’t always be fast. I live in California. I still have a little more time 🤣 don’t be scared, exercise and nutrition is so important 😊❤️ goodnight to you ❤️
❤🙏🏽🙏🏽🙏🏽🙏🏽🙏🏽
9:49
Multiple sclerosis is a fully treatable disease and is by no means an incurable disease.
Because modern medicine does not know the cause of MS, it is thought to be a difficult disease that cannot be cured.
I believe we can overcome MS today. God bless all !!
@@esclerosismultipleyenferme8790 i agree ❤️❤️ MS just needs us to be willing to take on the fight 🧡🧡🧡
Wrong. What are you thinking saying that?
So food is the only answer
?
@@MS.inspirational-ul9du I can’t help you see if you can’t. You were feeling best only with the keto/low carb and the hip exercise machine. So WHY change that? Your worst symptoms started AFTER taking those medicines but you seem to think you should listen to the Dr on that. You HaVE a CHOICE what you put into your BODY!
And I speak regarding this from experience
@@Elevatedpoetry not every gym has the multihip machine 😒 thankfully my husband got me one last yr on payments but by then my legs had already gotten very weak. My keto got extra lazy when COVID hit. The masks were not an easy thing to deal with and to leave my room I had to have it on. I’ve told my drs I don’t want medicine and they won’t take me off because “im worse without it” 🤬
@@Elevatedpoetry my heart is with you ❤️
- Oh sweetie, it's the holidays, we'll talk about it later....
What a jerk!!
Thank you 🤣❤️ more so to never return in the 10 days i stayed🤦🏻♀️
re you married or have family where you are? How can we help? GOD bless you; you are so brave.
@@joycewalbert1413 yes I am. My family is near. The best way you can help me is by staying strong 🧠 i can’t change my past, nor the decisions I made that led me and my MS to where it’s at. So please stay strong and never stop fighting. I hope my videos help and if they do, it make me very happy ❤️❤️❤️God bless you and thank you 😊
@@MS.inspirational-ul9du I will do my very best! I'm giving up most sugar now . Doctors always say I "look ok' . MRI looked bad to me. You stay strong and thank you so much for caring! 😘
I’m hoping you find something that works well with your MS symptoms.
I also have MS for a good few years and am having trouble with pins and needles in my feet, ankles, bottom and I’m sleeping an awful lot at the moment.
Stay strong we are all here for you my lovely X
I have been so sleepy lately as well but mine is due to major blood loss so I’m drinking a vegetable and fruit drink that has been helping with energy levels.
As im typing this reply I’m struggling to keep my eyes open 🤣 but I don’t give up easily. So, I took my pre workout and I’ll be going to the gym soon.
I don’t like to dwell on what I’m feeling, so I distract my mind. Learn new things, create different neuropathways. You can sing,dance, watch a funny movie, play games (i love candy crush 🤣)
Do whatever it is you like but distract your mind from those pins and needles. I know it’s hard just like I know simple is far from easy but it’s doable. Don’t let MS win ❤️ my heart is with you❤️❤️❤️
@@MS.inspirational-ul9du can i ask if pins and needles is a major symptom of ms please
Thx for sharing your journey. I checked out the book from library re: Wahl's diet when I was diagnosed 1-1/2 years ago. I am not strict, but do feel ok cutting out dairy and most sugars just like you:) We just keep on keepin on:) Blessings & love from Colo
Most sugars 🤣 that’s cute 😊 you understand 🤣❤️ i don’t do any diets now. I just try to not eat so dirty as in processed foods, refined or processed sugars. I don’t do much milk or eggs. Wahl’s diet is strict and my salute to those who do it❤️ my heart is with you ❤️ blessings and much love to you ❤️❤️
Why? Watch the first few minutes of your video again! The answer is there!
I pray that God gives you big healing hug and that he gives you a friend who can help you on your journey.
Thank you ❤️
They prescribed me the same or similar medication, that is an infusion every 6 months. What I am taking is called Ocrevus, but it might be the same thing just a different name brand. Yeah, I was concerned about the side effects of this medication. I have a lot of the same symptoms you have. Can't stand very long, walk with a cane, have bowel and bladder urgency and frequency, slurred speech that comes mainly with fatigue. with me, diet made no difference. I went keto for a year for different reasons. I did Keto to avoid prediabetes. Lost 30 pounds, but it had no effect on my MS.
I absolutely hate medicine. I am not a believer like many that dmts are necessary to feel better because out of the three medications ive tried ive just felt worse. Do you workout? Back in 2020 i was a gym rat and saw results, obviously not right away and i lived by no pain no gain. I went from a walker to cane to not needing anything but walking like penguin 🤣
to me exercise is #1 for me to see results in mobility. Nutrition is important but for me nothing works better than working out. Do you exercise? Start slow and work your way up. Consistency is key 🔑
What a beautiful soul you are... thank you so much for being so vulnerable and sharing your journey. God Bless you!!!
Aww 🥰 thank you ❤️ i try to be so people know they are not alone. God bless you as well 💕
No estás sola Bella 🙏❤️
You got this 💪 I’m here boo let’s GO GO GO
THANK YOU BELLA for sharing ❤
Thank you. You’re welcome 😊
Very glad to hear your story. You’re such a sweetie!
Thank you ❤️
Just ate a muffin. :(
@@MCATRealEstatePhotography don’t worry. I ate a frozen cheesecake 😄🙈 but flushed it water 🤣 so it must count…right?🤣🤦🏻♀️
@@MS.inspirational-ul9du That's correct. Maybe the water offsets the cheesecake. :)
You are not alone in this. You are a precious lady, it is so so hard bit you are doing amazingly and should be proud of yourself. Dont beat yourself up. Its hard to exercise and cook and clean when you are in constant fear and pain. You can do this! ❤
Thank you 😊❤️ i keep in mind that hard is not impossible 🧠
One of the hardest things is eating healthy when you can no longer cook for yourself. I'm alone and really the only things I eat anymore are highly processed foods like frozen meals and canned foods. I just can't afford to spend the money on expensive healthy prepared meals that are available. I wish you all the best as you find your way through this.
I completely agree! Do you like salads? That’s the easiest. Have you looked into the MS Society? They could help with their exercise scholarships if you’re approved. I was blessed to have chosen someone who is also a nutritionist. I know she’ll be able to help you 😊 Rita Allington (661) 803-0555
Hi..my wife is a vegeterian...what is the diet for ms that you have taken..any suggestons that can help...my wife was diagnosed MS in Jan 2023...
I was doing lazy keto trying to transition into paleos diet . The creator of the paleos diet has MS. You can’t go wrong with veggies, because of mixing some paleo into lazy keto i fell in love with veggies ❤️ does she watch her sugar intake? I use monk fruit with erythritol. Does she watch her carb intake? What about eating gluten?
My heart is with you two ❤️
I have severe nerve damage in my whole left side of body somewhat lik ms but not ms from 2 years. I got tests mri and everything is normal. Noone can help me am in agony without help n amswers i want to give up. Am just 40😢
My heart is with you ❤️ last yr I wanted to give up too and just put myself into vegetable state😢 but we can’t do that! While there is a way to fight keep fighting! A little goes a long way. Do you exercise? Do you cut foods out like processed foods? Are you surrounded by stressors? One thing that has helped me is sleeping and waking up with gratitude ❤️ sometimes it takes time to get a diagnosis 🥺 don’t give up ❤️ don’t let the enemy inside of you win! In my case MS. Before being diagnosed it was so frustrating seeing changes in me and drs not being able to help but as weird as it sounds sometimes it’s better 🤣 i got almost all MS symptoms once i started medicine. If I would’ve known just how important exercise is MS wouldn’t have attacked me like it did when i was lost and confused about what was happening to me.
@@MS.inspirational-ul9du no I can't walk normally forget exercising. Actually my condition my doctors are responsible. They put me on poisonous drugs couple of Years back that I didn't know. I trusted them I took now my left side body is heavily damaged.no diagnoses no treatment. Just on bed most of the time from 2 years. I ve no hope no solution no life no money. Lost my life lost My career. I just want peace from this mental trauma n life 😢 😭
I AM EXPERIENCING MANY SYMPTOMS. I feel blessed by your video
I go to the mayo Friday to discuss my concerns and hoping for an MRi. I have a daughter who has DS and all looking for a group home for her. This is in God's hands. God bless you.
How are you managing through your symptoms? I myself feel at my worst 🤣🤦🏻♀️ don’t ever give up❤️ my heart is with you both. This too shall pass ❤️❤️❤️ as i like to say “nothing lasts forever”
More strength and power to you ❤
Thank you ❤️
Brave sister
@@manijee3050 thank you ❤️❤️
I was diagnosed with MS at 21 but I was misdiagnosed at age 20
I was 24. How is MS treating you?
Dont you take plasma therapy.,...
No
Do you have hypomobility? Just lost my mum to severe ms i have fybromyalgia hefs just awaitung another mri results my mri just half hr
I was told “if you don’t know then it’s a no” 🤣 honestly, I think I need to work out like I used to as well as cutting foods out of my diet. Exercise repair myelin. My heart is with you ❤️❤️
There are ways to better your autoimmune (exercise, nutrition, the mind…). Stress is a huge one
@@MS.inspirational-ul9du so true I have asperger's I now no and that's caused some anxiety all my life
@@Truerealism747 the way i see things and I have to remind myself 🤣 if I can’t control it why stress. It is so not worth putting your body through that. It’s about looking forward and always gaining knowledge, to know and to keep your brain working ❤️
🙏🏻❤️🙏🏻
Dont give up please. Trust God amd pray everyday. Go back into keto diet and try intermittent fasting. Follow dr. Berg and other doctors that talk about hollistic medicine. People can be cured and have been cured of MS
Wow! You are one smart person! I’m impressed by someone who believes in holistic medicine and the importance of fasting. Nutrition and exercise are so important, MS or no MS. I love how you don’t go the medicine route ❤️
Hi, have you heard of dr brooke goldner and the nourishing green smoothie. She had lupus
Hello. No I haven’t. I will look that up thank you ❤️
@@MS.inspirational-ul9du I plan to try the green smoothie which is an anti inflammatory drink. I was diagnosed with MS on Oct 13 2022. We can all help each other live a long and good life, because it is possible!
@@bayskismith3720 do you drink turmeric? My heart is with you ❤️ exercise and lazy keto really help. Exercise repairs damaged myelin and lazy keto/ paleo really help im just at a point where im so confused with how my MS has been. Confused yet i know 🤣 don’t stress! It’s not worth your health ❤️
Be a fish and let things slide. Yes i agree and I appreciate you telling me about the smoothie ❤️
@@MS.inspirational-ul9du I have not tried turmeric. I do exercise at times. Exercise is medicine for MS (I heard from several sources).