DAG GONE IT ANYHOW! My MS symptoms won't ease up.
My speech is really draggy at times- hahaha--- great thing for a trainer. And yesterday, I sat in the middle of the bed, trying to remember my appts. for the day. And I had just looked at my calendar a few minutes before that. 
The worst is the vison issues. Most days - things just seem a "hazy" If I could get that to clear up-- life would be OK. Good thing is-- I don't always see the dust in the house! Well- good for me. Not so good when company is here! 
Just venting.... no big deal. Sometimes it just helps to write it down, and then forget it.  |
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| Hang in there!
Don't sweat the small stuff, especially if it is as small as dust. In the meantime... I'm glad you can type!  |
| Lori, I am so sorry to hear that you are suffering. I really wish that they could find a cure sooner than later. A friend of ours also has MS. He spends a lot of time swimming to help strengthen himself. I know he resisted going on the drugs for some time too trying to do more homeopathic treatments.
And please vent whenever you feel like it! |
| Lori, I don't have any advice for you...
Just a hug from the heart  |
| Lori, I don't have any advice for you...
Just a hug from the heart |
| I've got nothing but warm thoughts for you as well. **hugs**
Hang in there. |
| Warm thoughts from me too!
Did you see that article yesterday on MSN that said that a cancer drug slows the progression of MS? http://www.msnbc.msn.com/id/23170397/ |
| Hugs and kisses from me! This winter we're having is really having an effect on those of us with chronic neurology/muscular conditions. My fibro has been terrible. |
| Lori, I'm sorry to hear that you're still feeling so awful. I don't blame you for wanting to avoid the steroids - a family member has a neurological diseases and has had more long term problems from the steroids than the actual disease, Scary!
I hope you feel better soon |
| Hang in there!! it will pass as you know....until then...big hugs!! |
| Hugs to you, Lori. I wish there were something more tangible I could to to help you. Feel free to vent to us anytime. |
| Big hugs to you, Lori, as you face this difficult time. We are all here for you whenever you need us. Feel free to vent away at any time. |
| Sorry to hear, I have lupus so I know how terrible the steroids are. I've been on them daily for years. Prior to that I was able to do a dosage schedule similar to that used for asthma or an allergic attack. This wasn't nearly as bad as the daily regimine.
Hope you get over this flare quickly........Kathy |
Lori: I am sorry to hear you are still dealing with this "out break." I had so hoped that it has subsided by now. My daughter with the CMT seems to be having a rougher time of it right now too. Hugs to you until you get through this.  |
| I think the weather plays a big part in all of this.... |
| Hi Lori,
Before I got to the end of your post, I was thinking the same thing..weather plays a big part. Hopefully the sunshine is just around the corner! I wish I could find the right words or could offer advice - just wanted you to know you're in my thoughts.
I don't blame you in regards to questioning the steroid use. I'm wondering if you've checked out homopathic or naturapathic doctors and see if there are possible alternatives you can use? Marianne |
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Spring is around the corner and things will get better!  |
Lori, I'm sorry you're feeling so bad  . Maybe spring will be early this year so you feel better faster. |
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