Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
I haven't started the injections myself although I've heard that a Dr. Mark Stengler has written about a study. He had an MS patient who noticed a remarkable difference after one month of twice weekly injections and daily sublingual.
So, I started the B12 patch and I'm not sure if it's helping. How is the shot working out for you? Is it a pain to take it? How often are you doing it?
I think it's the best form of B12 from everything I've heard. I am looking forward to hearing how you do with it!
I have to do once a day for a week, then once a week for a month then once a month for a year.
My fatigue is so bad right now that I"m anxious to feel better and I know I"m just dreaming that I"ll notice any change this soon but once in awhile aren't we intitled to a little wishful thinking lol.
I'll keep you posted on how soon I start noticing a difference, and how things are going with them.
Thanks so much for caring enough to answer my question.
Kath
From what I've heard, the injections do sound promising so I'd be sure to write down all the detail of how you're feeling and then re-visit those notes in another month.
I have talked to others that have taken it and they said that they did not get a boost in energy either, but we also agreed that it might be becuase we are already really low, so that might play a part.
I do wish you the best and I hope it gives you the energy you need!
Best of luck! Lisa
I will write down daily in my journal how i am doing with them and we will see in a month how it goes.
Thanks Sweetie
Kath
I guess when your B-12 is low it's pretty hard to get it back to normal at least the high normal they want you at. The neuro did say I would feel so much better after taking the injections, wellllllll we will see.
I hope you feel better soon and good luck with your injections hon.
Kath
I"ll check with my Neuro who ordered this and if she can't answer me I"ll call the pharmacy. Seems funny I had fatigue real bad before the shots but not all this weakness.
Feel better soon Dear
Kath
So I guess I"ll call in the morning and see what she says.
The initial weakness I experienced during the first week is completely gone now and didn't last but just a few days.
I would strongly recommend using the intramuscular injections to anyone. The needles are very long but very thin.....painless.
I hope this helps.
Kath
NOW years later I had a conversation with my PT. She takes Trader Joes sublinguanal tabs. So I have started again. Take both B-12 tabs and B complex to do what I can to protect the nervous system.
Have you heard about the drug Amantadine? It was desinged to help avoid the flu but in some people it has helped with energy.
I am not going down the road of provigil/nuvigal. That didn't even work for me. But there are also supplements--creatine I think is one that works at the cellular level to help with energy. A neurology resident told me this. Looking this up I saw protandim too- Nicki posted about this some time ago and there is real science behind it.
There definately are non-drug strategies I just don't know enough about them. I am starting a new anti inflammatory/Dr. Wahls diet to see if that helps.
Hope this is not too much info!
Good Luck Kathi
Melanie
You also mention creatine. I had mine checked last night before my MRI's and it was also very low. They hestitated to give me the constrast due to this. I was told to drink plenty of fluids to help flush the contrast out of my body when I got home. Don't know if this is the same that you are referring to or not or if it has anything to do with low B-12 or not. Just thought I"d put that out there.
Be well
Kath