Yes to so many things you said in this video! Always listen to your intuition, ask questions, stay positive and continue to aspire to be and do all that you want! I have had NMO for almost 15 years. It takes a toll for sure. It absolutely sucks sometimes but my longest periods between relapses have been when I'm consciously eating healthy, minimizing stress and staying happy by doing things I enjoy. I haven't made any videos about NMO yet because I haven't been able to bring myself to talk about it but I hope to do so soon. Thank YOU for sharing your story. I didn't comment on the earlier one but I watched that too. I hope you are feeling wonderful!
Oh Meg - you are so impressive in this vid / SO Mature and SO well spoken.. I am so very proud of you and happy at the wonderful progress you are making in your interesting life!! Lots of love to you!!!! ❤️❤️❤️
thank you Megan! i had also a rare autoimmune disease called MOG.and yes we have the same condition especially our eyes.but thank you for sharing your story.and we will continue to praise and thank God for He has saved us.and He really loves us.God bless and yes we need to be positive always :)
Question, I have ms which is also an autoimmune disease that affects the brain spinal cord and optic nerves, is nmo the same? If not do u know what differentiates them?
Good question! MS and NMO are sometimes called sister diseases, because they are very similar at times. However, MS and NMO are treated completely different. MS medications and treatments won't usually stop or help relapses for NMO & may even cause further damage. Unfortunately, many MS patients are misdiagnosed and suffer the consequences as a result. Hope this helped answer your question!
Yes to so many things you said in this video! Always listen to your intuition, ask questions, stay positive and continue to aspire to be and do all that you want! I have had NMO for almost 15 years. It takes a toll for sure. It absolutely sucks sometimes but my longest periods between relapses have been when I'm consciously eating healthy, minimizing stress and staying happy by doing things I enjoy. I haven't made any videos about NMO yet because I haven't been able to bring myself to talk about it but I hope to do so soon. Thank YOU for sharing your story. I didn't comment on the earlier one but I watched that too. I hope you are feeling wonderful!
Hi. Do u still have nmosd?
@@allahallah6427 yes, I do
Did uh take treatment for NMO,and how it diagnosed
Thanks for your videos give me strength to continue and know that I am not alone with this disease
Oh Meg - you are so impressive in this vid / SO Mature and SO well spoken.. I am so very proud of you and happy at the wonderful progress you are making in your interesting life!! Lots of love to you!!!! ❤️❤️❤️
thank you Megan! i had also a rare autoimmune disease called MOG.and yes we have the same condition especially our eyes.but thank you for sharing your story.and we will continue to praise and thank God for He has saved us.and He really loves us.God bless and yes we need to be positive always :)
Question, I have ms which is also an autoimmune disease that affects the brain spinal cord and optic nerves, is nmo the same? If not do u know what differentiates them?
Good question! MS and NMO are sometimes called sister diseases, because they are very similar at times. However, MS and NMO are treated completely different. MS medications and treatments won't usually stop or help relapses for NMO & may even cause further damage. Unfortunately, many MS patients are misdiagnosed and suffer the consequences as a result. Hope this helped answer your question!
@@megwoolf yes it helped alot! Thank you for answering. I guess that makes us warrior sisters as our illnesses are so closely related. 😊
@@megwoolf can anyone suffering from nmo have normal life span in future or he or she may die early? Plz do reply plz
Hi Megan, i love you.