Multiple Sclerosis ~ Update : March 22, 2009
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9:44
Beautiful Brain.movby Rufusinski1,600 views- 7:10
Official Diagnosis : RRMSby mom2kaylantristn1,386 views
- 6:46
Living with Multiple Sclerosis - Tysabri B & Aby laurenvparrott2,652 views
- 2:43
P1030052.MOVby LoveActually28456 views
- 4:44
Copaxone Injection - Day 2by mom2kaylantristn2,430 views
- 4:31
Shared Solutions Info & Auto Ject 2by mom2kaylantristn1,636 views
- 7:01
My MS Storyby eclipsedeyes3,769 views
- 3:21
Copaxone Injections - MSby LoveActually288,761 views
- 2:59
Copaxone injection for Multiple Schlerosisby kusemf8,969 views
- 3:25
Three lesions walk into a brainby thehappycovv370 views
- 3:11
In Memory...by mom2kaylantristn335 views
- 3:39
29 Gifts by Cami Walker: How Giving Can Change Your Lifeby ExpandedBooks7,759 views
- 2:40
Copaxone Injectionby Bulbheadthegreat19,048 views
- 8:48
Living with Multiple Sclerosis: My 6thTysabri Infusion and my Garden Roomby angelusa73963 views
- 3:31
Re: MS Diary 12by soulsoup1234321 views
- 9:53
Newly Diagnosed with Multiple Sclerosis 2 0f 5by MSVlogSupport313 views
- 9:01
Multiple Sclerosis Injection Tips (Comedy Sketch)by Fripodaca30,599 views
- 4:57
Day 1by mom2kaylantristn2,412 views
- 7:06
Copaxone Injection - Day 3 - Right Hipby mom2kaylantristn23,787 views
Hello, I am on Betaseron this is the same type of medication as Rebif because it is an interferon. I also have depression but I take an anti-depressant so that helps. The injection site reactions with Betaseron haven't been that bad and as long as I take advil about an hour before I inject I feel just fine. It has worked well for me so far. It has been about a year now. Good luck with everything!
FritoCat 2 years ago
Good luck with your decision. I am taking Copaxone every day - would that be an option for you as opposed to 5X/week?
jlbb1 2 years ago
Doesnt Copaxone take almost 1 year to start working? Does your dr feel that the disease will progress too much to wait and see?
Reluctantwriter7 2 years ago
Thank you for the new video. I was wondering how you'd been doing. I actually stopped taking my Copaxone, for different reasons (well, the site reactions were horrible). I just don't believe in my case of MS that the DMD's provide me a benefit. I'm managing with diet/exercise and managing my pain with other drugs.
dmplaura 2 years ago
be aggressive with the medicines. look at tysabri. also check out a youtube video by holly huber about stem cells. good luck.
cliff501 2 years ago
hey thanks for the update, i'm new here! Just wanted to say I'm on Betaseron and although I only just started my doc said that the depression thing is an unlikely side effect. I suffered from major clinical depression in my teens so I was a bit cautious but as he says the immunotherapy is stressful and having the disease is stressful and it's quite possible the depression that people experience is often caused by that rather than the actual medicine. Good luck with making your decision. F
eclipsedeyes 2 years ago