Aug
6
Multiple Sclerosis: It’s not THAT bad! 1/2
Posted by admin Comments (21)
Talking about multiple sclerosis and how I cope with it. I would like to correspond with others with MS through YouTube. This is just me talking about how lucky I am to be alive and how MS cannot take away my appreciation for the awesome gift of life.
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Categories: What Is Multiple Sclerosis
Im here to tell you that i am extremely moved by this video….Everything from you explaining the medical side of ms and the emotional and trying times that we all go through..I was diagnosed with secondary progressive ms in august of 2007….And the comments you were talking about appreciation are soooo true…..I never take anything for granted, knwoing that someday it will be taken from me….forgive me for the lengthy comment….This video reminds how lucky i am..Ione(iown) Marie
Ione,
Thank you so very much for your kind words. I appreciate that you took the video for what it was. A message saying that MS cannot take away the zeal for life that we have.
God bless you.
Please do not apologize for a long comment. I encourage them.
As I said in the vid. I am rather long-winded myself.
Your friend,
IRISH
great vid..i’m subbing
Thanks. It was my first video.
I am proudest of another video that I encourage EVERY person with MS to watch.
It is called;
Multiple Sclerosis; The Greatest Crippler of Young Adults?
Check it out.
I do appreciate your kind words.
God bless.
Irish
I don’t have MS but I found this video fascinating, not only from an educational standpoint but you have also really have helped me re-evaluate my life and my priorities. Thank you.
Thank you.
I am glad that you do not have MS!!!!!
MS is my cross to bear. We all have one.
This video can be helpful when you start to take the gift of LIFE for granted.
You do not have to be sick,
You just have to be HUMAN to get something from this.
IRISH
p.s. I checked your channel and I love your song.
Thank you very much indeed.
Hello, I am going through the motions of possibly being diagnosed with MS. I struggling with a burning eye amongs other things. The burning has left me with a tingling, burning sensation together with my vision going from 20/20 to slightly blurry to getting better again. Can you help me and share your experience? Cheers,
Andy
irishbear, thanks for this video. My first symptom was double vision and problems with walking. When I had my first MRI the neurologist was thinking of a tumor and I was afraid. But everything was okay. No tumor. Than they thought it could be ms, but they could not find proof after tests. So I lived my life. And years went by without exacerbations. But than things worsened. And now I am diagnosed with ms (primary progressive).
Thanks for your video and positive message. MS is not that bad.
I would be happy to talk to you about my experience and I would like to talk with you.
God bless,
Mark
Thanks for watching.
I can bear whatever is thrown at me.
It is the Christ in me that is positive.
Personally I am miserable until Christ strengthens me to face this disease.
As long as I keep plenty of room for God in my heart, this disease can do nothing to me.
Mark
You are right! Amen.
Sorry im commenting on all you vids, but i am enjoying watching them.. now VERTIGO, i had something like that a few times over the past few months. I didnt eat oysters but i explained to my nueroligist, nurse and doc and they said its not MS and they didnt give me any explantion. could you please give me more information on Vertigo please.. wow that vertigo really freaks me out.. thank you very much..
No worry, little brother. Comment all you like.
Vertigo is from when your CEREBELLUM gets inflamed. Your cerebellum help you balance and you orient with your surroundings. I am absolutely shocked that they did not think your vertigo was associated with your MS. IT WAS MY FIRST SYMPTOM!!! The raw oysters carry a bacteria that can cause your immune system to kick it up a notch (this proves it is autoimmune to me)
In fact, men more often have cerebellar involvement than women
2nd opinion, man.
Thank you, information is helpful. Next time I see my nurse I will mention what you have replied and see if she realizes what it is. Again thank you very much..
Amazing video!
I was diagnosed last year in October at the age of 22, and it is one of the hardest things to hear. I had no clue what MS even was, and after the news sinks in it can be very bleak. The most important thing in my life was my support group. My family, my husband, and my in laws.
Once you come to terms with the diagnosis, you do come to realize it isn’t the end of the world. Yes, it sucks, but you could have something much worst, so I’ll take it over something like cancer.
Having your family with you is very important.
My wife has been my rock. It is good to hear that your hubby and other family are your source of strength.
i have really relied on God too in these last 6 years.
I hope you are well.
KEEP TRUCKIN’
Mark
Just found this video…wish I’d found it about a year ago. I did lots of searching on the web when MS was mentioned but never thought to check youtube for info. My MS is annoying-especially at the moment-but for the most part, it’s not that bad. I’ve been very calm through it all but I wonder/worry ifwhen the day will come that I have a total melt down For now it’s all one day at a time.
It is very very clear that the cure for MS is on the horizon.
A discovery in Italy assures me of this.
Check out chronic cerebral spinal venous insufficiency and the Liberation Procedure.
Dying in an installment plan?.hmmm Give me quick death instead.but there are diseases/conditions out there much worse than MS. Generalized/cervical or any kind of dystonia,ALS,parkinsons,msa,alhzimers,huntingtons,wilsons…
Basically as f’d up as MS is, its actually one of the lesser on the totem as far as administering misery to the sufferer when it comes to issues of the CNS. . I’m 80% sure I have this condition I just cannot prove it. Campath1H a real DMD imo is the answer.
ur heads gonna explode