Saturday, November 21, 2009

Follow Up On Some Research

Here is a very good summary about "Research into Blood Flow in the Brain and Venous Insufficiency, or CCSVI, in MS".

This research was in the news a couple of months ago and several bloggers did discuss it. I find this article is written in plain language. Well, as plain as any scientific research can be made. There is also a FAQ list that you might find helpful.

My understanding is that blood flow problems may be causing the inflammations that result in myelin damage. The researchers are building on studies that were abandoned years ago, as MS research moved toward studying the immune system causes of MS. This does not mean that current research is misguided nor that the old research was useless. It means (to me)that perhaps there is a new way to resolve the MS question and come up with treatments, that would lessen the need for the powerful drugs that are now used to combat MS. In future, a procedure such as one used to unblock clogged arteries might help relieve MS and prevent further symptom episodes. Not a cure, but a step in the right direction

I am posting this today aware that it is old news, however this article and the FAQ's really cleared up some of the questions I had about this research. It's possible my interpretation is wrong. That's why you should read it for yourself and decide. I am not an MS expert as some blogger claim to be. I am trying to find something positive, that can make me and maybe others, feel a little more hopeful about our situation.

It might have to do with me feeling better about things these days and make up for all the whining I do.

Thursday, November 19, 2009

The Results

The neuro appointment went smoothly My balance is not so great and my reflexes aren't either, otherwise physically, things aren't that bad.

My doctor wants to try mega doses of vitamin D. This seems to be the latest treatment for MS. I have to have a blood test first and then will most likely take about 4,000 units a day to start. I was just too tired to go for the blood test today. I'm already taking 1,000 units a day as a supplement, so I'm part way there.

I don't know what the big deal was about the Health Canada report. The doctor there DID, recommend for me to work at home and my neuro DID, give a diagnosis of relapsing remitting MS. Yes, there was a suggestion I go see a psychiatrist but that was not mandatory, as my employer insisted. I discussed it with my doctor and he said that's a standard recommendation when an individual is diagnosed with an illness like MS.

I explained to him that at the time (last fall) I was so stressed out about my work situation that I was depressed and I did feel suicidal. When you are losing half your pay cheque due to illness and your employer is stone walling, on top of the MS, that would make most anybody depressed. Regardless of how low I was feeling, I would never have killed myself.

What happened is instead of trying to resolve my work situation my employer focused on one thing. Lets pack her off to a shrink and he will fix her up. If that doesn't work, we will pension her off and be done. Not sure if it's lack of caring,laziness, or both. Luckily, a court case( Lloyd vs CRA) came along just at the right time to help me out. Now things aren't that bad at work. I'm at home four days and one day in the office per week.

I've decided to move on and look ahead. Will I forgive and forget ? NO !!

Wednesday, November 18, 2009

I Said Doctor, Doctor, Mr MD

Have my Neuro appointment in the morning. Not exactly over the moon about that.
What's the point? At least I will finally get my hands on the Health Canada report I had to fight so hard to get released. Tonight I don't feel like a bag of bones. I feel like a piece of raw bacon lying around.

You want a nice, no whining blog ? Sorry, guess you will have to go elsewhere.

Tuesday, November 17, 2009

Dignitas

Not much in the mood for writing. Way too tired. Here's an interesting article about the Dignitas clinic in Switzerland. 80% of people who get permission to end their life decide not to That's how effective the counseling is. We need to have a dialogue here in Canada to allow assisted suicide No I'm not contemplating it. I just think it would be worthwhile to know that if things were really bad I could die with dignity.

Sunday, November 15, 2009

It Started With A Mirror

Watching the silent version of "The Thief of Bagdad' with Douglas(hunk) Fairbanks.
These silents films have been given a boost with new music soundtracks

It started with the installation of a new mirror. I was at a discount decorating store on Saturday looking for Christmas cards, and noticed a dusty mirror sitting in a corner. It was such a good deal I couldn't resist. Oval shaped with an ornate antique gold coloured frame. Today I put it up and it looks pretty snazzy. Had one of those rare bursts of energy, so next thing you know I'm practically reorganizing the entire upstairs of my house. Managed to conquer the dust bunnies too. The weather was bad out otherwise I would have gone for a long walk. It was so nice to feel good for a few hours. I hit the wall around 3:00 and couldn't do much after that. Still, tonight I don't feel so bad.Tired but not weak.

I think my feeling good is partly due to my THC vapour knocking me out, which allowed me to have a nice long sleep on Saturday night. I am only using it a few times per week in the evening at stronger doses, rather than every day mild ones. Saturday I was in so much pain with the sensation of a nail being shoved up the bottom of my left foot. Decided I may as well have a good stiff shot of vapour and it worked. My foot calmed, my twitchy leg relaxed, and I fell asleep. Nice !

The beauty of it is I wake up the next morning and I don't feel like a zombie like I do when I take sleeping pills. Haven't had one of those in awhile and I don't miss it. Don't miss the yucky metallic taste in my mouth either.

Haven't had much time for my blog and when I have time, I don't have the energy. This week I had seriously considered packing it in. I wonder if there is any point to this blogging? Well, here I am at it again.

The weather continues mild. Saturday was like a spring day. I know it won't last. The Santa Claus parade was today and snow is just around the corner.

Wednesday, November 11, 2009

The Energy Audit

No, not on me, although I could use one. This audit will allow me to get a rebate from the government when I install a new furnace, which looks like I'm going ahead with. Getting a new central air unit too, thanks to MS. Meaning, that I always thought of air conditioning as a luxury and now I see it as a necessity.

On December 1st it will be bye bye, to the old clunky furnace and noisy air conditioning unit. Plus I should save some money on my gas bill.

Got the Swine Flu shot today. It was pure fluke. I was in the mall on my way to the bank and noticed another clinic . It was so quiet, not like the long noisy lines of the last two weeks. I thought what the heck, may as well get one. I was in and out in less than five minutes, aside from the twenty minute wait after the shot.

Remembrance Day
" Never Forget - Never Again"


The Berlin wall fell without any violence. Why can't we resolve all issues that way?

Tuesday, November 10, 2009

MS Update

Well it is called Carole's MS Blog, which I haven't had the energy to update.

I am soooooooooo tired. Not sleepy tired. Weak, bag of bones, tired. I have one good day were I get busy and then one horrible day were I can barely move. Even now I don't feel liking typing this. Only doing it because next week I have to see the neuro and I want to remind myself of how awful I feel.

AND how many people come to me for advice. I help them yet nobody can help me with this. I suppose if I was rich and had servants it would be less bothersome. Only I don't and lots to do, only I don't have the strength. It sucks !!!!!!