Thursday, December 30, 2010
Multiple Sclerosis been good to me in 2010 and I pray it continues in 2011. Yes, I have had my moments, but it has not been as bad from previous years. There is no doubt in my mind, God does not give us more than we can handle. I know my MS behaved this year because my husband has been going through a lot medically in 2010. I am thankful I had been able to be there for him as he has been there for me when my multiple sclerosis is at its worse.
The unconditional love I feel for my husband, I would gladly have my multiple sclerosis rear its ugly head so he would not have to have any more surgeries or health problems. I cannot see my future without him. Therefore, my wish for 2011 is for the return of my husband's good health, continued better days than worse for me and my virtual friends living with or without Multiple Sclerosis.
See you all again in 2011!
Tuesday, December 14, 2010
If you had been reading the blog you know, every now and then I post a Did-U-Know, which is my way of passing on some fantastic consumer information news...
After the birth of my first born in 1982 my breast size went from a 36DD to (warning put your drink down now) to 38K. I could not buy a brassier from a regular store; I had to purchase my brassieres from specialty lingerie stores. To me carrying around all those breasts were a curse to everyone else it was envy from woman and sexual gawking from men.
I carried my large twins nicely for many years because they were supported with the best money could buy. However, I had enough of unwanted sexual advances and carrying the weight, so I made a decision against my husband wishes to have a bi-lateral breast reduction. I felt like a new person after my surgery and it was wonderful being able to shop for a brassiere at a regular store again. I became a Victoria Secret gal, I could not get enough of purchasing brassieres from The Secret until I tried a Maidenform, and my preference is their Lilyette Minimizer collection. The secret to Victoria Secret is their brand is overrated. You have to give credit where credit is due when it comes to VS, they have a damn good marketing department.
Anywho, after all these years of being a Maidenform gal, I never knew about the lifetime warranty on their products. I had recently purchase another Lilyette and one of my snaps broke. Instead of throwing the bra away, I contacted the company. I was ecstatic to hear about their lifetime warranty; all I could think of was how much money I threw away over the years when I no longer used a particular style Maidenform brassiere. I felt like a kid in a candy store when I went through my lingerie draw and pulled out the Lilyette brassieres I no longer wore and mailed them off to Maidenform a week ago. Maidenform wasted no time in replacing my brassieres. I received my replacement brassieres TODAY!
All you have to do to replace a Maidenform product is:
Provide your name, address, and phone number inside the package you are returning. I also provided a size and style change for one of the brassieres I sent to them.
If you do not wear Maidenform brassieres and know someone who does PASS THIS ON TO THEM!
Monday, December 13, 2010
If I did not believe, Copaxone was slowing the progression of my multiple sclerosis. I would not be taking the daily injections. I quit injecting Copaxone in my right buttock two years ago. As of December 7, 2010, I will no longer inject Copaxone in my left arm. It is now December 13, and my left arm is still sore. Immediately after removing the needle from my arm, my arm went limp, pain radiated from my shoulder blade to my fingernails. Trying to lift my arm was like trying to pick up a ton of bricks. I counted the minutes thinking to myself, "In about 15 minutes I should be able to move my arm." I sat in bed watching the clock; it was two hours before I could lift my arm to my face and several hours later before I could lift my arm over my head.
During that time a strange sensation flooded my body, my brain felt like a circuit breaker going haywire, then an extreme fatigue invaded my body, a fatigue I am still experiencing as of today. I have been doing great and feeling fine when I was not taking my injection after my flu shot occurrence. Yes, I had some pain here and there and slight immobility because of nerve pain in my foot during my hiatus from taking a Copaxone injection. Where there is belief, there is doubt, I am questioning is all this is worth the unknown of what happens after an injection.
There are times I do not know what to do when it comes to treating my MS. I do know I will not be taking an injection in my left arm again. There are only five other places I can inject Copaxone. Unless, for some other reason...If or when I experience what recently occurred when I injected my left arm and what I experienced after an injection in my right buttock over two years ago happens in the remaining places I have left to inject.
Regardless of my belief...
There will be no reason for me to continue taking Copaxone.