Experiences with

Betaferon

I am quitting my DMT. I take Betaseron and randomly get hit with flu-like symptoms. This unpredictability gets debilitating. Anyway, I have gotten 3 months at a time, and am stopping at the end of one month. So I have two months of unopened meds that I hate to just throw away. Does anyone know of

G'day ms siblings. Are YOU smiling? If no. why not? SMILE. We all have the opportunity for a treatment option today. When I started Australia only had Beta Betaseron or nothing. Today that is very different, we have options. Our ms has options it can be slowed down. How GREAT is that

G'day ms siblings. Are YOU smiling? If no. why not? SMILE. We all have the opportunity for a treatment option today. When I started Australia only had Beta Betaseron or nothing. Today that is very different, we have options. Our ms has options it can be slowed down. How GREAT is that

G'Day. I guess I should answer the question for YOU who do not know. Firstly who I am NOT. I am NOT your Doctor, or a doctor of any sort. I have knowledge of Relapsing Renitting ms (RRms) on a very personal level. I am where YOU are now 20+ years ago. I have a spouse 2 years ahead of me.

I started long ago on Betaseron\betaferon. Interferon beta 1b and I have the scarring to prove it. The wife likes to tease me about all the lumps in my butt. No soft fat for her to pinch. Ahh well this is life with a chronic incurable disease.

I don’t know about advice, but I can tell you my experience using Tysabri. I have been receiving an infusion—Tysabri—for at 13+ years. After my diagnosis only the ABC drugs—avonex, betaseron and copaxone—were available and I had intolerable symptoms. My doctor recommended Tysabri which was new at the

I remember when I was on Betaferon\betaseron for years I took ibuprofen religiously before injections and a meal. To advert side effects. The4se are SERIOUS medicines that we take. Protect yourself, BUT take them.

Good Morning my beloved ms family. If “YOU” are new that is “YOU. If “YOU” have been around for a while “YOU” know how I feel about “YOU” and this family in particular. Yes, “YOU” are cared about by a complete stranger. Let us all be clear. I am not any type of medical professional. There

The ONLY medicine available at the time was Interferon Beta 1b, Betaseron or Betaferon depending where “YOU are in the world, and I was an absolute coward when It comes to needles and they asked for one every other day. Well eventually I pulled my head In gritted my teeth and did it.

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Hi everyone! I am Jean. Diagnosed in 1995, I was 45. When drugs were available it was betaseron on lottery. Waited until choices were ABC. Chose A. On it until 3years ago. Suddenly the every 2 yr followup showed multiple new lesions. No idea when during the 2 years or if gradual or sudden. No

I have had MS for 29 years and have done fairly well. I was on Betaseron for several years, then switched to Tecfidera, but my liver function numbers were not good. I then switched to Copaxone. I am currently taking nothing. My white blood cell count is low. My blood platlet count is low. We are taking

Interferon Beta 1b Betaseron or Betaferon depending on where"YOU" were in the world. Same stuff different names, marketing issues I guess. The next year I believe Avonex then Copaxone came along.

Silly but is a coping mechanism Just like DMT (Disease Modifying Therapy) or ABC’s (Avonex Betaseron\Betaferon. Copaxone) or Tec (Tecfidra) is. Make things smaller easier to handle and come to terms with. I do not start at 150 kilogram (300 pounds) weight at the gym.

It is okay. How "YOU" feel is okay. This is your illness; these are your feelings, your fears. I do not expect "YOU" or anybody to understand mine. No matter how close they may be to me. I live in my head. My feelings and fears are mine. At 3 am when I can not sleep for whatever reason

Why anybody with Relapsing-Remitting ms (RRms) would not lead a happy and fulfilling life. Come to think of it anybody with RRms today in 2018 particularly. There are so many medicines available to "YOU", I just had "B" Betaseron, then for years the A B C's. I was so happy when Tecfidera came on

I am not a Doctor of any sort. RoyceNewton RoyceNewton• in a few seconds•0 Reply This is my opinion, ignore it if "YOU" do not like it or it does not suit "YOU", I am always okay with that. In my twenty years living Relapsing Remitting ms(RRms) life I have picked up one or two pieces of advice that I

This is my opinion, ignore it if "YOU" do not like it or it does not suit "YOU", I am always okay with that. In my twenty years living Relapsing Remitting ms(RRms) life I have picked up one or two pieces of advice that I might like to pass on to "YOU" either newly diagnosed(newbie) or someone in the

hello again, yes I am back with yet still more to tell "YOU" AS I will say, again and again, I am "NOT" any kind of professional. These opinions are mine from forty plus years of combined experience, Mine (male) and she who must be obeyed (female) so if there is a medical issue see a doctor, I am

msers, to just be polite I have been strongly told that I should inform people a little about me. Basically, things that I am 'not" and how I come by my opinions and beliefs. 20 years having travelled this, my ms journey has given me the belief system that I have. I have learned that it can be rather