Does Having Multiple Sclerosis Make Us Unlucky? Not On Your Life!

61

By jmebish

Does Having Multiple Sclerosis Make Us Unlucky?

Does Having Multiple Sclerosis Make Us Unlucky?

Not On Your Life!

The last couple of days my MS has been kicking my you know what, the symptom that lead to me being diagnosed have returned with a vengeance and brought along a friend.

Along with the numbing sensation that passes through my head repeatedly it is now accompanied by an audible sensation doing the same thing.

Both are very odd sensations that basically incapacitate me momentarily, the problem being they tend to come one after another for a period of time sometimes for hours with little break. The sensation feels like every neuron in my dead is firing at one time.

In addition my emotions have been incredibly out of whack and turning me into quite the jerk. I talked with my Betaseron nurse a few days ago and discussed my continuing symptoms.

Faces of MS

It has been over 4 months since this attack first started and I have not really seen a reduction in symptoms, they just seem to change from one thing to another.

My nurse told me that with Betaseron, as I am sure with the other interferons as well, some patients have their symptoms start to fade within a few weeks of starting the medicine, others do not see much if any change until 6 months when the medicine is supposed to really start taking effect and still others do not have their symptoms lessen or go away and all the medicine affectively does it help stop further damage from being done.

Well I know I am not one of the lucky ones in the first group, so now I wait and see what group I will be in.

Funny, I say lucky ones but is it strange to consider anyone with MS lucky? Well if not then that is a poor outlook on life. We may have MS but that does not mean we are not lucky, I am lucky for being alive, I am lucky for my wonderful family and I am lucky that things are not worse. No matter your situation there is always someone else who has it worse.

I am not in a wheelchair like so many MS patients and although I may stumble a bit I am still able to walk and even run when there are those with MS who can’t. Even those with MS who can’t walk or run or are in a wheelchair, even those people are lucky, they have their lives and they have the love and support of myself and millions of other MS patients around the world

Comments

Jen's Solitude profile image

Jen's Solitude Level 3 Commenter 3 years ago

Hi Jamie, Sorry to read you are in a flare. I do think being on Beta will help you, maybe not with this particular flare, but in other ways. I started on Beta and stayed on it for about 8 months.

Don't forget how important it is to REST, I can't emphasize that enough. Fatigue will make any flare increase. The symptoms you have when newly diagnosed take quite awhile to settle down, afterall the symptoms are what finally got you diagnosed, showing it is no little problem. So along with learning how to rest more, add patience to your symptom relief plan. Let some time go by before you decide your current flare will not pass.

Also may I suggest finding a good online support group so that you can find out what others with your symptoms do for relief.

If you need a suggestion for an online support group just let me know.

Take care now, and please take it easy.

lovezan profile image

lovezan 3 years ago

MyMSLife

Very nice hub. I really enjoyed it.

If you have some times please visit my site

Health care share with you

http://tanyangsheng.cn/

Submit a Comment
Members and Guests

Sign in or sign up and post using a hubpages account.



    • No HTML is allowed in comments, but URLs will be hyperlinked
    • Comments are not for promoting your Hubs or other sites

    Please wait working