My MS story

Thank you for sharing. I have MS and was diagnosed 3 years ago. It's very lonely because it's an invisible illness- people assume you're fine. I feel bad almost all of the time, but look normal. No one wants to be the person to complain, but it is such an awful illness. Tired, dizzy, nauseous, weird heart beat, major back pain, difficult to breathe- every day is hard. I hope there is a cure during my life. And I want to know: why did this happen to us? I used to be a runner. I could run so fast and felt so free. It's all I want again. I would give anything for that feeling. Anyway, thanks again for sharing, it makes me feel less alone.

Hello! Thank you for this video! I'm going through something very similar to the beginning process of your MS story as well. My symptoms aren't the typical optical neuritis, I see most people with that symptom get diagnosed a lot faster than us with "invisible" symptoms such as pain. I've yet to get diagnosed but I have a gut feeling its MS and they're just chalking up my symptoms to anxiety but I will keep pushing until I get proper tests. I'm super glad to see that your channel is still active! I came here for your MS story but will be staying for your beauty content. Please continue to post vids and keep us updated on how you're doing. Much love. 💕

God Bless Dear ! May you you live a very happy life ahead !

Aashild, I’m so sorry and you were dealing with this for so long with no proper diagnosis. Thank you for sharing your story with us! I know there are many out there that can relate with you; feeling alone and scared. I’m so glad that you found the proper diagnosis! I just want to give you such a big hug right now😘

You are so brave to share your experience. I have a cousin who was diagnosed with Fibromyalgia in her 20’s and she was finally diagnosed with MS in her late 30’s. She just had another infusion last week. She gets them every 6 months. When I had my health scare last year, a lot of the symptoms I was having sounded like the same as MS. It was actually the first conditioned I googled trying to diagnose myself. I feel very lucky that my condition was treatable. MS is horrible. Again, thank you so much for sharing. 💕💕💕

This is quite powerful . Thanks.

sending prayers your way🙏 just saw your video brought me to tears

Thank you for sharing. One of the best videos on the subject.

Oh my! Are we MS twins. Your story is basically my story from the start to end..wow! Thank you for sharing 🦋

Thank you so much for sharing your story. I’m so very sorry the doctors didn’t listen to you which made you feel like you were weak. You are clearly incredibly strong and brave - your honesty is very powerful. Klemmer x Jane - I was diagnosed April this year.

It’s ok babe, you’re not alone ! ❤️😔😢

First of all, I can only imagine the strength and energy you had to post this video. As a person with MS, I find thinking hard drains me more than any physical activity and to post this in your non-native tongue is incredibly impressive!! I really appreciate you sharing your story! How many years between your first doctor visit about your symptoms and your diagnosis? I knew a lot of what you were going to say before you said it because that is how I felt... like relief to get a diagnosis. I was too relieved to be depressed about it. I also find it interesting that someone as "healthy" as you, couldnt get diagnosed sooner because OBVIOUSLY something is going on if you dont suffer from many other illnesses. I was fortunate that my regular doctor didnt guess when I came in and both of my hands were numb and not doing what i told them. As a person who is significantly overweight, I was ready for her to say that was the cause. But she sent me to a neurologist with a specialty in MS. I was diagnosed right away. But I have had a hard time getting doctors to listen to me abt my back pain. It took getting such severe leg pain (abt 8 years later) that I was treated for that and that treatment helped my back. This is a very hard illness to have being that each symptom COULD be MS or something irrelevant. I wish you lots of luck and support as you travel thru with it.

You are so pretty. I wish you all the best. We are in this together. We have ms it doesn't have us. Stay strong 🧡

Thank you for sharing as you seem like a lovely lady.

Thank you so much for this video. ✨❤️

Thank you so much for making this video and sharing your personal story. I have been having symptoms on and off for years and am just now thinking I might have MS. I have been having medical issues since I'm little and not sure if they are all linked. I had seizures as a kid, puberty at age seven-but didn't get my period until I was twelve when I had it for two weeks straight(almost needed a blood transfusion), stopped getting my period at sixteen years old( diagnosed with polycystic ovarian syndrome, gastric ulcer, and depression), in 2002 had seizure in college( first one since I was 8 years old-diagnosed with sleep apnea), in 2009 have severe sinus infection and asthmatic bronchitis, then pneumonia with severe vertigo for months, few years ago lost feeling in the outside of my left thigh with pain, pin and needles feeling, fatigue, memory problems, lately having been having pins and needles randomly on and off in my hands and feet with numbness, headaches, more dizzy on and off, not remembering people I have met before, palpitations, an episode of my legs feeling wobbly and weak( having to sit down). After Christmas I plan on talking to my doctor but I'm nervous about it. Thanks again! 💕

🖤 thank you for this story

Intense stuff ... you sound strong and ready for this, though! I'm posting a "my MS story" video this week, too, so found yours inspirational and full of ideas. Hang in and take things as they come ... you've got this!

Oh wow! I can totally relate to you! I was diagnosed with fibromyalgia in 2004. Always tired and always sick but I did not have much pain , which I thought was weird because I had a friend who had fibromyalgia too. In 2011, I started with balance problems and falling a lot. Then heat sensitivity . For the past few years now, I’m in constant pain. My hip is killing me and sharp shooting pains in my feet ,neck, head…I had 2 MRI’s done 1 for the brain and 1 for the spine but have to wait till September to get my results. Like you I have been feeling like I am crazy or it’s just in my head. People probably think I make things up?! I hope I get some kind of diagnosis if it isn’t MS. I need to know so I can move on and do what I have to. Thanks so much, you are very inspirational!!

I'm going through same sickness and Dr jerking me around ...GOD BLESS YOU FOR PEACE HEALING JOY TAKE CARE ❤