Greetings. I was fortunately just recommended this video by TH-cam. I, too, have that four letter acronym as a constant companion but I am nowhere near as cruelly impacted as you were. I am very sorry that you had to suffer so tremendously for so long. Your recovery is absolutely remarkable. You possess levels of fortitude and determination that are far statistical outliers. You are one of those rare folks that possesses true grit. I applaud you most heartily on being so steadfast. You are undeniably a Superwoman. Please do continue to thrive. Smile often and be of excellent cheer.
You are an incredible inspiration for all people dealing with a devastating neurological disease like CIDP! I was recently diagnosed with CIDP and MGUS in October and it has progressed so quickly it has been scary. I came across this video trying to educate myself on what I should expect. Now anytime I start to get depressed about it or begin to lose hope, I re-watch your video and it inspires and humbles me at the same time. Thank you so much for sharing your story. You are an amazing person!
I am diagonosed with SIDP from Nov 2019 and it's progressive.my legs becoming weak day by day, doctors gave me steroids ivs but condition is not changing so far.hoping for speedy recovery.
God bless you. Beautiful video. I went through the same thing in 2017 through to 2018. 8 months in hospital 6 months in icu. With good support and resilience i made a full recovery. Stay stong💪❤🙏
Wow Courtney, I am super impressed how you recovered from that devastating condition. I feel your pain, I went through GBS, which I always thought was CIDP and know exactly how frustrating is for someone full of live and love. Always stay positive and smile like you did on the video. I truly love the fact that many people think that life stopped still and was over at the moment they were diagnosed and experienced the symptoms. But, you did went above and beyond to recover and get better, and never stopped smiling at life. I was diagnosed in 2011 when was still very uncommon and no Doctor knew how to well treat the condition. I have overcome bad depressions for not being capable to do the same things I used to do. But, looking at your video today is big proof of faith and motivation for me to never think that nothing is impossible. Shears and please never stop smiling!!
Yasss oh my goodness yass! Saw a quote today that ties in with this. "Be GENTLE with yourself ... you're doing the BEST that you CAN!" ~ source unknown ~
I live in South of France and today is Friday may 17th, 2019 and I comment from my hospital bed suffering from a miscarriage which started from monday, 3 days after my husband and I found out that the pain he has been feeling since September 2018 is CIDP. We started researching and voila. Your video has giving me new hope and renewed my faith. Thank you for sharing.
Hi Courtney, my wife and I just watched your video. YOU are AMAZING!! I was diagnosed with CIDP in 2016 and have been struggling with the adjustments that must be made. I was pretty active, and I miss all my outdoor activities. I continue to workout, when I have the energy, in hopes of going back to work and resuming activities. Thank you fore your transparency and willingness to make and share this video. You are a beautiful woman inside and out!! God bless you Courtney!! Sincerely, Jack B.
My, my, Courtney, your words are magnificently true. I laughed and cried (a little) for the first half of your video. '...yes to dance beneath the diamond sky with one hand waving free'. You made it! You've given the absolute best of yourself; you recognize the beauty of your opportunity to see people at their very best. Understanding, seeing and feeling unconditional love...look at you now. Congratulations!
I’m crying! How beautiful you are. You’re a strong lady and even through what you’ve been through you still find positives. May you live a very happy beautiful life. ♥️
Thank you so much for your story! I love how you were able to mentally stay strong. Im struggling with that the most more than physically. I have lost everything and I don’t know where/how to rebuild.
I love your strength and you Courtney. You have given me the strength to fight and make my physical body better. I thank for that. You made me love life again after watching you.
Hoy te conocí por medio de estos videos y estoy muy feliz de haberlo hecho, no sé si haya alguien con tu fuerza, tu energía y tu valor te admiro y te agradezco sinceramente espero algún día poder saludarte.. Eres increíble. Un abrazo
I’m currently recovering from CIDP, I got diagnosed officially on June 8 but I had started to notice weakness in my legs since March. My upper body was not really effected much which I am so grateful for and seeing your recovery is incredibly humbling and emotional. I am so in awe of the strength you had to recover from such a difficult condition and with so much positivity. It is a great reminder to me to not be so hard on myself and get frustrated with the rate of my recovery, I feel determined to make a full recovery and your video has brought me a new found motivation thank you so much for sharing your story
You are awesome Courtney. You give hope to struggling people. Great video documentation and inspiration. Had the nerve test and am awaiting the spinal tap, truly scares me as this dizzy deadness is progressing.
first of all... super duper is the coolest name ever. second, youll be ok. it never feels that way in the beginning, but you will. i post waaaay more on my unicort FB page if youre interested and i have a FB group called "we are greater than" that's pretty uplifting if you want to join
You are such a beautiful, radiant person, inside and out! I just came from a drs appt where CIDP was mentioned as a suspected culprit for my weakness, numbness, tingling, unsteadiness, etc. and now we're working on getting Lumbar Puncture procedure set up for next few days or week... I'm honestly terrified. Never even heard of CIDP ... thought I was going in for 4th MRI today, so I was blindsided and overwhelmed. I found your video on TH-cam, and I just fell in love with you! You give me hope and courage, Courtney. I felt like you were talking directly to me when you said if you are living your life thinking about what could have been, or focusing on what you're missing, you're not getting it. You're missing out on your life now! Oh my gosh -- what an ephiphany moment that was for me. You're EXACTLY RIGHT... and I have been stuck in this rut for over a year. Sorry to write you a novella instead of a brief comment, but I had to thank you, Courtney. God bless you and keep you strong and thriving. I subscribed to your channel. ❤❤❤❤ Looking forward to more videos.
Joan Steakley girl, you are going to be ok! This is going to give you what everyone is craving in life - strength, meaning, substance, and purpose. I post much more on Facebook if you want to find me there. My name is Courtney Runyon ❤️
you are my new inspiration, just being diagnosed today, not fully but the neuro is 95% positive just needs the confirmation that i have CIPD. but seeing you come this far, inspires me. i was literally in tears watching this!
Bless your heart. You are one strong woman!! I actually have a neighbor who was diagnosed with this and then unbelievably, her husband was just did agnosed with it about a week ago. So rare for husband and wife to have both been diagnosed. I believe about four years apart.
Hi Courtney, You are SO STRONG. I'm very grateful I found your video! I'm 33 and today my feet are flippers. No confirmed diagnosis yet, but my neuro explained to me what CIDP is and the symptoms line up too well. I want to tell you, Courtney, that even if my situation never progresses to the extent of yours, I hope with all my heart that I can have a fraction of your grace. Thank you 💜
I was diagnosed with CIDP 3 days ago. You give me the courage that I desperately need right now. I also have the swallowing and difficulty speaking symptoms like you, and seeing you be able to speak normally and walk again really fills me with hope. Thank you for sharing.
I also have cidp and I've had it for 8 years now and it SUCKS! Thank you for sharing your story you are such an amazing human being and God bless your soul!
I also was diagnosed 1 year ago, but had symptoms for about 4 years prior to that. So far I haven't responded well to the treatments. Thank you for the inspiration to keep going!
Hello, my 4yo got cidp when he was 3. He lost control of his feet. With ivig he's slowly getting back where he can walk with braces. His left foot came back and it was bent over stiff. He had surgery on his Achilles tendon so his foot would fit into a brace well. Thank you sooooo much for sharing!!! Your an inspiration!!!
Thank you for the video… I am 6 months into my ‘treatments’ for CIDP. I am transitioning from IVIG to Rituxan because the monthly infusions of IVIG aren’t getting the job done. My symptoms aren’t as severe as yours. I can sort of walk. But thank you for the encouragement.
Hi, thank you for your beautiful post. I am fighting through CIDP as we speak. After recovering a bit I just had a setback and whas mentally at an all time low. Just saw your video and I feel motivation to not give up again. I hope 2019 will be as great as you hope it is in the end of your video. All the best
You are an incredibly blessed woman with an incredible family. Your experience has enriched you with an appreciation of real love. The mountain you've climbed 10,000 times is nothing more than a hill soon and your story is a blessing to everyone who have followed your progress. I wish you receive everything - the desires of your heart, for sharing your amazing story.
I cried during watching the video. I understand how hard it’s to lose everything around you, when you feel yourself abnormal anymore. I’m a CIDP patient for 14 months right now and i don’t know how and when I’ll go back to normal life again.
I’m 16 and I have cidp since I was 11. My cidp always relapsing every 1-4 months after ivig until now. I love your inspiration story so much! thank you for sharing this 🙆🏻♀️ (sorry for my english)🇲🇾
Hola Courtney ! Te envío un fuerte abrazo desde Monterrey, Nuevo León, México. Fui diagnosticada con CIDP en enero de este año y estoy en tratamiento con Inmonoglobulina. Mi puercazo (Así le llamo de cariño a mi cuerpo😁), me advirtió que algo pasaba y gracias a Dios me trataron en la etapa inicial por llamarlo así. Como mencionas, tuve un año 2018 de mucho estrés y el CIDP me hizo reflexionar sobre demasiadas cosas de mi vida. Te envío muchas bendiciones, eres hermosa, una guerrera y tu actitud es lo mejor. Me tomaré el atrevimiento de compartir tu video en mi face. Un abrazo 🤗. Bendiciones 🙏
I cried throughout your entire video. Newly diagnosed with CIDP. This is the scariest thing I've ever been through. Your video is inspiring. Question tho. You said your disease was caused by stress. Can you tell me more about that? It would definitely make sense for me as well. But unfortunately I haven't received many answers to my multiple questions.
Hola este video es de mucho valor y ayuda para los que tenemos CIDP, solo quisiera pedir de favor si se puede, que se ponga la opcion de traducir al español.. para ayuda de los que no sabemos muy bien ingles... muchisimas gracias.
hello I was diagnosed in 2016 after 8 months and 23 days in USC and I am 90 % Curd thank God . But I still have norathapy in my feet and I can’t pend ( squat down ) I know how hard it is god bless u
Hi, my best friend is actually going through the same thing she was diagnosed in the end 2017 going into 2018. She had lost all feeling in her hands first then in her legs. It has been over a year since she had been diagnosed. She has regain some function in her legs, she has to walk with braces and canes. She still can really lay her feet flat on the heel because her nerves aren't recovered. With pt she gained the use of her hands again. Everything so far with her plasma treatments it has been helping her make her recovery. But lately she has been depressed and so frustrated, I keep telling her that everything is going to be okay you've come this far. But it's just not working is there anything that you recommend for her to do or for me to help her do? Thanks
Maria C Is she still improving? Or is it up-and-down? Find me on Facebook. I check the messages there much more often - “Unicort” is the name of my page
I love your spirit. I am a girl going through some hardships and can relate to health struggles. I hope you are so proud of yourself. You are amazing. Your figure is absolutely beautiful too. I wish you happiness and continued healing in 2019.🌸
Hi my name is Argy I’m 19 and suffer from a brain injury that affects my daily functioning do you have any tip on keeping my thoughts straight on what my goals are
Your story sounds like you had GBS..... because I had it, with the exact symptoms..... in 2007. I 'fully' recovered, but now, 15 years later I am developing the same symptoms, slower progression thought. How long did it take for your symptoms to get worse...? days? weeks?
Mi padre el 2013 fue diagnosticado, con esta enfermedad, y su esfuerzo , fe en Dios, trabajo medico , ahora hace su vida , prácticamente normal, con sus medicamentos al día y sus controles lleva su vida casi normal, es una enfermedad muy terrible, pero se puede llevar.
Hi Ma'am my Husband is suffering from CIDP since 2015.He have still footdrop in both legs and lower limbs..He used a couple of year Predisolone And he got little bit recovery ...Can You suggest me the best Exercise for these diseases if Then Help me🙏🙏🙏🙏❤❤❤❤ You are really amazing Inspiring women I am From Nepal
I was diagnosed with CIDP when I was 12 years old, now I'm almost 20 years. And I walk with AFOS since then. In my case it's impossible to fully recover from it.
Michelle Longo I can’t remember, but I don’t think so. My feet got swollen sometimes and my hands. And they would get cold from bad circulation. I’ve heard of peoples feet turning blue though
Thank you replying It was nice to see that my brother condition was something out there, his onset had been slow but he has his up and downs happens to be back in hospital getting a plasma treatment
Greetings. I was fortunately just recommended this video by TH-cam. I, too, have that four letter acronym as a constant companion but I am nowhere near as cruelly impacted as you were. I am very sorry that you had to suffer so tremendously for so long. Your recovery is absolutely remarkable. You possess levels of fortitude and determination that are far statistical outliers. You are one of those rare folks that possesses true grit. I applaud you most heartily on being so steadfast. You are undeniably a Superwoman.
Please do continue to thrive. Smile often and be of excellent cheer.
You are an incredible inspiration for all people dealing with a devastating neurological disease like CIDP! I was recently diagnosed with CIDP and MGUS in October and it has progressed so quickly it has been scary. I came across this video trying to educate myself on what I should expect. Now anytime I start to get depressed about it or begin to lose hope, I re-watch your video and it inspires and humbles me at the same time. Thank you so much for sharing your story. You are an amazing person!
I am diagonosed with SIDP from Nov 2019 and it's progressive.my legs becoming weak day by day, doctors gave me steroids ivs but condition is not changing so far.hoping for speedy recovery.
God bless you. Beautiful video. I went through the same thing in 2017 through to 2018. 8 months in hospital 6 months in icu. With good support and resilience i made a full recovery. Stay stong💪❤🙏
Wow Courtney, I am super impressed how you recovered from that devastating condition. I feel your pain, I went through GBS, which I always thought was CIDP and know exactly how frustrating is for someone full of live and love. Always stay positive and smile like you did on the video. I truly love the fact that many people think that life stopped still and was over at the moment they were diagnosed and experienced the symptoms. But, you did went above and beyond to recover and get better, and never stopped smiling at life. I was diagnosed in 2011 when was still very uncommon and no Doctor knew how to well treat the condition. I have overcome bad depressions for not being capable to do the same things I used to do. But, looking at your video today is big proof of faith and motivation for me to never think that nothing is impossible. Shears and please never stop smiling!!
what you said about forgiving yourself for not achieving an unrealistic goals hit me so hard.
thank you .
Yasss oh my goodness yass! Saw a quote today that ties in with this. "Be GENTLE with yourself ... you're doing the BEST that you CAN!" ~ source unknown ~
I live in South of France and today is Friday may 17th, 2019 and I comment from my hospital bed suffering from a miscarriage which started from monday, 3 days after my husband and I found out that the pain he has been feeling since September 2018 is CIDP. We started researching and voila. Your video has giving me new hope and renewed my faith. Thank you for sharing.
Hi Courtney, my wife and I just watched your video. YOU are AMAZING!! I was diagnosed with CIDP in 2016 and have been struggling with the adjustments that must be made. I was pretty active, and I miss all my outdoor activities. I continue to workout, when I have the energy, in hopes of going back to work and resuming activities. Thank you fore your transparency and willingness to make and share this video. You are a beautiful woman inside and out!! God bless you Courtney!! Sincerely, Jack B.
My, my, Courtney, your words are magnificently true. I laughed and cried (a little) for the first half of your video. '...yes to dance beneath the diamond sky with one hand waving free'. You made it! You've given the absolute best of yourself; you recognize the beauty of your opportunity to see people at their very best. Understanding, seeing and feeling unconditional love...look at you now. Congratulations!
I’m crying! How beautiful you are. You’re a strong lady and even through what you’ve been through you still find positives. May you live a very happy beautiful life. ♥️
I love your message. Thank you for sharing and I wish you all the best.
Thank you so much for your story! I love how you were able to mentally stay strong. Im struggling with that the most more than physically. I have lost everything and I don’t know where/how to rebuild.
You are a beautiful in side and out. God bless you.
Through it all, you never lost your incredibly high cuteness factor. Cheers!
You're a wonderful woman. and an inspiration for many people who are going through the same thing.
I love your strength and you Courtney. You have given me the strength to fight and make my physical body better. I thank for that. You made me love life again after watching you.
Hoy te conocí por medio de estos videos y estoy muy feliz de haberlo hecho, no sé si haya alguien con tu fuerza, tu energía y tu valor te admiro y te agradezco sinceramente espero algún día poder saludarte.. Eres increíble. Un abrazo
You look so pretty Courtney you have come a long way since I met you Hope you get everything you want you're a super beautiful woman
Just found this. Beautiful. Thank you for putting it out there. Your friend. David B. 😉
You are my inspiration Court! I can't wait to see you hike the Camino!
I’m currently recovering from CIDP, I got diagnosed officially on June 8 but I had started to notice weakness in my legs since March. My upper body was not really effected much which I am so grateful for and seeing your recovery is incredibly humbling and emotional. I am so in awe of the strength you had to recover from such a difficult condition and with so much positivity. It is a great reminder to me to not be so hard on myself and get frustrated with the rate of my recovery, I feel determined to make a full recovery and your video has brought me a new found motivation thank you so much for sharing your story
You are awesome Courtney. You give hope to struggling people. Great video documentation and inspiration. Had the nerve test and am awaiting the spinal tap, truly scares me as this dizzy deadness is progressing.
first of all... super duper is the coolest name ever. second, youll be ok. it never feels that way in the beginning, but you will. i post waaaay more on my unicort FB page if youre interested and i have a FB group called "we are greater than" that's pretty uplifting if you want to join
Thanks for the encouragement! May just have to get on board with FB and the group. Physical Therapy..day one, here we go.
God bless this woman she is so awesome and she’s a fighter. Your a great person and a inspiration much love from Kentucky
You are such a beautiful, radiant person, inside and out! I just came from a drs appt where CIDP was mentioned as a suspected culprit for my weakness, numbness, tingling, unsteadiness, etc. and now we're working on getting Lumbar Puncture procedure set up for next few days or week... I'm honestly terrified. Never even heard of CIDP ... thought I was going in for 4th MRI today, so I was blindsided and overwhelmed. I found your video on TH-cam, and I just fell in love with you! You give me hope and courage, Courtney. I felt like you were talking directly to me when you said if you are living your life thinking about what could have been, or focusing on what you're missing, you're not getting it. You're missing out on your life now! Oh my gosh -- what an ephiphany moment that was for me. You're EXACTLY RIGHT... and I have been stuck in this rut for over a year.
Sorry to write you a novella instead of a brief comment, but I had to thank you, Courtney. God bless you and keep you strong and thriving. I subscribed to your channel. ❤❤❤❤ Looking forward to more videos.
Joan Steakley girl, you are going to be ok! This is going to give you what everyone is craving in life - strength, meaning, substance, and purpose. I post much more on Facebook if you want to find me there. My name is Courtney Runyon ❤️
@@CourtneyRunyonUnicort Yes, Miss Unicort, I found you and followed you on fb already! Thanks for the sweet reply and for the inspiration! Much love!
you are my new inspiration, just being diagnosed today, not fully but the neuro is 95% positive just needs the confirmation that i have CIPD. but seeing you come this far, inspires me. i was literally in tears watching this!
Bless your heart. You are one strong woman!! I actually have a neighbor who was diagnosed with this and then unbelievably, her husband was just did agnosed with it about a week ago. So rare for husband and wife to have both been diagnosed. I believe about four years apart.
Becky Cook wow that’s insane
Hi Courtney,
You are SO STRONG. I'm very grateful I found your video!
I'm 33 and today my feet are flippers. No confirmed diagnosis yet, but my neuro explained to me what CIDP is and the symptoms line up too well.
I want to tell you, Courtney, that even if my situation never progresses to the extent of yours, I hope with all my heart that I can have a fraction of your grace.
Thank you 💜
Thank you for sharing your story what a miracle you are blessing dear AMAZING so much to be thankful for sure
like number five from Brazil. Follow you. Very proud of you. Keep going. Good vibes from my tropical country
I was diagnosed with CIDP 3 days ago. You give me the courage that I desperately need right now. I also have the swallowing and difficulty speaking symptoms like you, and seeing you be able to speak normally and walk again really fills me with hope. Thank you for sharing.
I also have cidp and I've had it for 8 years now and it SUCKS!
Thank you for sharing your story you are such an amazing human being and God bless your soul!
I also was diagnosed 1 year ago, but had symptoms for about 4 years prior to that. So far I haven't responded well to the treatments. Thank you for the inspiration to keep going!
You're incredible...
Great story
Hello, my 4yo got cidp when he was 3. He lost control of his feet. With ivig he's slowly getting back where he can walk with braces. His left foot came back and it was bent over stiff. He had surgery on his Achilles tendon so his foot would fit into a brace well. Thank you sooooo much for sharing!!! Your an inspiration!!!
Freakin awesome!!! I’m speechless You are doing so good I’ve said it to you before your so inspirational! Keep fighting
You are so so SWEET:-) GOD BLESS U !
I love this! Thanks for sharing ❤️❤️❤️❤️❤️
God Bless you!
Thank you for the video & speech in the end.
❤ you are a rock star babe. Stay strong CIDP sista ❣️
Your Awesome!!!!
Stay Strong!!
I have a friend going through the same thing gonna show him you video..
Hope you're feeling alright haven't heard from you in a couple months You do look super pretty
You are an inspiration and such a nice person
Thank you for the video… I am 6 months into my ‘treatments’ for CIDP. I am transitioning from IVIG to Rituxan because the monthly infusions of IVIG aren’t getting the job done. My symptoms aren’t as severe as yours. I can sort of walk. But thank you for the encouragement.
Hi, thank you for your beautiful post. I am fighting through CIDP as we speak. After recovering a bit I just had a setback and whas mentally at an all time low. Just saw your video and I feel motivation to not give up again. I hope 2019 will be as great as you hope it is in the end of your video. All the best
You are an incredibly blessed woman with an incredible family. Your experience has enriched you with an appreciation of real love. The mountain you've climbed 10,000 times is nothing more than a hill soon and your story is a blessing to everyone who have followed your progress. I wish you receive everything - the desires of your heart, for sharing your amazing story.
Thanks congratulations for your courage and fight....
Wow very inspirational story!!
I cried during watching the video. I understand how hard it’s to lose everything around you, when you feel yourself abnormal anymore. I’m a CIDP patient for 14 months right now and i don’t know how and when I’ll go back to normal life again.
I’m 16 and I have cidp since I was 11. My cidp always relapsing every 1-4 months after ivig until now. I love your inspiration story so much! thank you for sharing this 🙆🏻♀️ (sorry for my english)🇲🇾
Thank you for this video - I can personally relate as this is also my story.
Hola Courtney ! Te envío un fuerte abrazo desde Monterrey, Nuevo León, México. Fui diagnosticada con CIDP en enero de este año y estoy en tratamiento con Inmonoglobulina. Mi puercazo (Así le llamo de cariño a mi cuerpo😁), me advirtió que algo pasaba y gracias a Dios me trataron en la etapa inicial por llamarlo así. Como mencionas, tuve un año 2018 de mucho estrés y el CIDP me hizo reflexionar sobre demasiadas cosas de mi vida. Te envío muchas bendiciones, eres hermosa, una guerrera y tu actitud es lo mejor. Me tomaré el atrevimiento de compartir tu video en mi face. Un abrazo 🤗. Bendiciones 🙏
Sandra soy de Monterrey también y me diagnosticaron Cdip, me gustaría platicar con alguien con mi misma enfermedad
Sailing in the same boat dear...Big hug from India....❤❤
You recover so fast. I can't wait until I walk again. I'm a paraplegic. One leg is weaker then the other
yeng lee From autoimmune or spinal cord injury?
@@CourtneyRunyonUnicort I'm not sure you have both?
I cried throughout your entire video. Newly diagnosed with CIDP. This is the scariest thing I've ever been through. Your video is inspiring.
Question tho. You said your disease was caused by stress. Can you tell me more about that? It would definitely make sense for me as well. But unfortunately I haven't received many answers to my multiple questions.
Hola este video es de mucho valor y ayuda para los que tenemos CIDP, solo quisiera pedir de favor si se puede, que se ponga la opcion de traducir al español.. para ayuda de los que no sabemos muy bien ingles... muchisimas gracias.
I love your story, I have CIDP and live in Nevada. I’d love to talk with you if you have a little time.
hello I was diagnosed in 2016 after 8 months and 23 days in USC and I am 90 % Curd thank God . But I still have norathapy in my feet and I can’t pend ( squat down ) I know how hard it is god bless u
I have suffered two bouts of Guillain Barre. (43 days on a ventilator). I am doing well now. I hope you are also doing well.......
Hi, my best friend is actually going through the same thing she was diagnosed in the end 2017 going into 2018. She had lost all feeling in her hands first then in her legs. It has been over a year since she had been diagnosed. She has regain some function in her legs, she has to walk with braces and canes. She still can really lay her feet flat on the heel because her nerves aren't recovered. With pt she gained the use of her hands again. Everything so far with her plasma treatments it has been helping her make her recovery. But lately she has been depressed and so frustrated, I keep telling her that everything is going to be okay you've come this far. But it's just not working is there anything that you recommend for her to do or for me to help her do? Thanks
Maria C Is she still improving? Or is it up-and-down? Find me on Facebook. I check the messages there much more often - “Unicort” is the name of my page
You are my hero.
I love your spirit. I am a girl going through some hardships and can relate to health struggles. I hope you are so proud of yourself. You are amazing. Your figure is absolutely beautiful too. I wish you happiness and continued healing in 2019.🌸
How do your arms feel an update please?
What’s the name of song?
So inspiring!! ❤️
Hi my name is Argy I’m 19 and suffer from a brain injury that affects my daily functioning do you have any tip on keeping my thoughts straight on what my goals are
Fuera excelente que pudiera subtitularlo al español, tengo este diagnostico y lamentablemente en mi pais hay muy poca información. Me siento sola 😞
Your story sounds like you had GBS..... because I had it, with the exact symptoms..... in 2007. I 'fully' recovered, but now, 15 years later I am developing the same symptoms, slower progression thought. How long did it take for your symptoms to get worse...? days? weeks?
Hi ! Did you recover totaly ?
You are so strong
不错，加油
Mi padre el 2013 fue diagnosticado, con esta enfermedad, y su esfuerzo , fe en Dios, trabajo medico , ahora hace su vida , prácticamente normal, con sus medicamentos al día y sus controles lleva su vida casi normal, es una enfermedad muy terrible, pero se puede llevar.
I bet your therapist's consider you the hi lite of their careers fearless joyfulness in one package
Was diagnosed with CIDP last week at age 74
I have some questions can you help
Hi Ma'am my Husband is suffering from CIDP since 2015.He have still footdrop in both legs and lower limbs..He used a couple of year Predisolone And he got little bit recovery ...Can You suggest me the best Exercise for these diseases if Then Help me🙏🙏🙏🙏❤❤❤❤ You are really amazing
Inspiring women I am From Nepal
Suprina Tamang th-cam.com/video/sNP_j4_E3h0/w-d-xo.html
I was diagnosed with CIDP when I was 12 years old, now I'm almost 20 years. And I walk with AFOS since then. In my case it's impossible to fully recover from it.
hi can i ask a question?
Rex1014 GT Of course
@@CourtneyRunyonUnicort how many months before your fully recover? or years
I ask a question because i have cidp ,and my hand i cant move and my feet
Rex1014 GT if u have any questions please ask me I want through hill but I’m 90 % Curd God bless your soul
Did you ever have dropped feet
your hand have spastisity?
Rex1014 GT no, but I heard that CBD is great for that
What is CBD?
@@mhandrexariola7039 its weed oil
Did you have where your feet turn blue and purple
Michelle Longo I can’t remember, but I don’t think so. My feet got swollen sometimes and my hands. And they would get cold from bad circulation. I’ve heard of peoples feet turning blue though
Thank you replying It was nice to see that my brother condition was something out there, his onset had been slow but he has his up and downs happens to be back in hospital getting a plasma treatment
You... Just you ❤️💋kin titanium
I hawe cidp thanks for movie it s beter