Contact Me at

Dear Readers,

 

You may email me at:

MS.Comments@AllAboutMS.ca

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Responses

  1. Hi,

    My student Miranda L. needs a diagram for a powerpoint on the central nervous system. May she copy yours and use it, if she gives credit to the source?

    Thanks.
    Mrs. Linda Riesenberg
    North High School–Sioux City, IA

  2. do you know anything about PGL (Persistent Generalized Lymphadenopathy) or swollen glands with no other symptoms? I have heard that MS can cause this. I have had a swollen neck gland for over a month, not sure what doctor to work with. Thanks

  3. oi am vdey interested in strm cell therzapy for multiple sclerosis

  4. How can I get this stem cell therapy for M.S.? I’m desperate.

  5. BONNIE WHAT IS IT WITH THE FDA AND REFUSING THE FABRIDINE PILL? OR DID I MISUNDERSTAND SOMETHING.

    SANDY

  6. Sandy, you are correct. FDA did refuse to okay Fabridine.

  7. JUST READ YOUR RESPONSE TO ME ABOUT THE REFUSAL OF FABRIDINE BY THE FDA, DO YOU KNOW IF THEY HAVE COMPLETELY CANCELLED IT OUT OR ARE THEY STILL CHECKING THE DRUG OUT?

  8. I WROTE YOU ON APRIL 14TH ASKING IF YOU KNEW IF FABRIDINE WAS COMPLETELY CANCELLED OR ARE THEY STILL CHECKING IT OUT?
    PLEASE RESPOND.

  9. For your answer please check out my other blog: http://multiplesclerosis.blogharbor.com

    I am no longer posting to this blog. See: April 12 posting.

  10. I WILL NOT POST TO THIS BLOG ANY MORE:

    IF YOU WANT ANSWERES TO YOUR COMMENTS PLEASE GO TO THE URL LISTED BELOW.

    I have another blog that I have been posting to for the last three years. It has much more information on it. I am sorry but it has become a chore to attempt to post information to both blogs. Therefore, I have decided to quit posting to this blog and post exclusively to my older blog. The URL for my other blog is:

    http://multiplesclerosis.blogharbor.comPlease enter this new blog into your favourites.

    I usually post anywhere between 2 and 7 times a day to this other blog.

    Your answer was post on April 12th, check it out.

  11. Hi, I am still checking it out. But, as far as I can find the company has to do more research and studies. I will post information as I find it on my other blog.

  12. hi i have a spinal tap done tommorow and im scared to death this is all new to me but i am glad i found ur site i just hope mine goes like urs did

  13. hi i go for a spinal tap tommorow and im scared to death i am glad i found ur site i just hope mine goes like urs did

  14. i was told in 1999 I had MS well now that its worse I don’t know what to do or where to go the doctors give me a steroid in a pill form and when I have an attack I am taken to the emergency room and givin a IV then sent home I don’t have medical help or insurance. Im scared. my daughter sent me a book on MS and the or my journey, well I read it and have found out that I really need a lot of help because I don’t know waht to do now. I just know I am scared. I normally stay in my appartment and go NO where.can you help me. I don’t want to be like this I sleep or when I”M awake I cry.

  15. Dude this blog rules i cant believe i finally found what i was looking for, thanks bro.

  16. Hi Mary, could you please tell me more about your symptoms? Please remember, I am not a medical person. I am a person who has MS also.

    Bonnie

  17. I just turned 60 and have had MS since I was 32 I am currently on Ampyra but would be interested in the stem cell therpy. I still work full time and walk with a cane for the last 3 years.

  18. I will investigate more way for people to get into stem cell research and stem cell therapy.

    Please remember, I am a patient with MS, not someone who is works in the medical field. I endeavour to bring you information via this blog to allow you to have as much information as possible.

  19. Hey everyone, I am a family practice physician that has been unable to to practice medicine due to the anxiety that I have determined to be be a direct result of my primary MS exacebation which happened in 1997. I have since been unable to function in high stress jobs, and am currently employed as a medical support asst., and not very proud of it. I know my anxiety disorder started when my first disabling exacerbation happened in 1997, as a medical resident. Since then, I have only had success with controlling the anxiety through beta blockers. I have had no success with any anti drepressive medications, and I think they just add to the overall problem by altering moods, and changing hormonal balance….This is just my opinion, but I have lost my livelyhood to practice medicine because of this overwhelming anxiety that I experience, and I thought someone might appreciate to hear from someone else who has the same issues…..Taking daily Beta blockers has helped significantly, as far as my ability to still work and function productively, but I know that the anxiety disorder is directly related to my MS lesions and /or the initial exacerbation while I was a medical resident. (high stress times) I’m Ron Rieder, and anyone can contact me with info, or questions anytime…thanks. ronaldrieder@HOTMAIL.COM

  20. I just want to tell you that I am just beginner to weblog and actually loved your page. Very likely I’m going to bookmark your blog post . You absolutely come with beneficial well written articles. Appreciate it for sharing with us your blog site.

  21. 57

    I was looking for some support and someone who understands the distress that comes from ms bowel problems, it looks like I’ve found it. Thanks, I’ll be back.

    Dx 1984


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