Ms, anemic level, vitaminD level , thyroid problems, avonex
Posted: Sun Jan 20, 2013 3:24 pm
Hello,
I am 37 and been diagnosed with ms about year and a half ago. It took over a year to diagnosed with 3 Nero opinions. All came up with ms, I suffer from tiredness, dizziness, numbness, swallowing issues , pain, lots if body pain, memory loss, tremors, handwriting has changed drastically, ms hugs, losing feeling in limbs, seeing black spots and this is just things off the top of my head. I just started avonex this last Friday night, that was a mentally hard one! I pre medicated and sat. Felt pretty horrible, today Sunday I'm feeling better. I also have a low vitimain d, I take 50,000 iu 3 times a week, I struggle with that often. I had a low b-6 level that is now maintained with supplement. I have thyroiditis that my endocrinology dr says can be caused by ms. I have so far had one wing removed. I am anemic, tomorrow afternoon I get infusions of iron, which is better than a transfusion. I was diagnosed by process of elimination and a brain MRI. Foci in the bunches, lesion in white matter of brain. Ruled out any other possibilitys of brain lesions and other symptoms. I have has every test under the son. I have gotton much worse in last couple year, ms is day to day in my life reminding me what I have been dealt:( has anyone else dealt with anemic with ms? Thyroid issues ? B-6 and d vitimain difficiacys ect . I yeah wanted to mention, Fridays avonex was only 1/4 dose, this Friday 1/2 dose , the 3/4 dose then full!! Yikes ! And then changing to pen! Anyone have that experience ? Thank u and god bless:) one more thing I would like to add, I see alot of people on this site that push the natural way by diet, supplements, remedies ect. Which I think is great if that works for u. I tried for over a year and have gotten at least 40% worse by listening to those ideas. Last option was avonex, I have realized that there all kinds if levels and Mis diagnosing if ms. I feel that mild cases can be treated more at a natural level , why other cases can not and need to be addressed with an aggressive
Approach. I wish I would of done that route as well as my changes in lifestyle. That is just my experience, it does not work for everyone.
I am 37 and been diagnosed with ms about year and a half ago. It took over a year to diagnosed with 3 Nero opinions. All came up with ms, I suffer from tiredness, dizziness, numbness, swallowing issues , pain, lots if body pain, memory loss, tremors, handwriting has changed drastically, ms hugs, losing feeling in limbs, seeing black spots and this is just things off the top of my head. I just started avonex this last Friday night, that was a mentally hard one! I pre medicated and sat. Felt pretty horrible, today Sunday I'm feeling better. I also have a low vitimain d, I take 50,000 iu 3 times a week, I struggle with that often. I had a low b-6 level that is now maintained with supplement. I have thyroiditis that my endocrinology dr says can be caused by ms. I have so far had one wing removed. I am anemic, tomorrow afternoon I get infusions of iron, which is better than a transfusion. I was diagnosed by process of elimination and a brain MRI. Foci in the bunches, lesion in white matter of brain. Ruled out any other possibilitys of brain lesions and other symptoms. I have has every test under the son. I have gotton much worse in last couple year, ms is day to day in my life reminding me what I have been dealt:( has anyone else dealt with anemic with ms? Thyroid issues ? B-6 and d vitimain difficiacys ect . I yeah wanted to mention, Fridays avonex was only 1/4 dose, this Friday 1/2 dose , the 3/4 dose then full!! Yikes ! And then changing to pen! Anyone have that experience ? Thank u and god bless:) one more thing I would like to add, I see alot of people on this site that push the natural way by diet, supplements, remedies ect. Which I think is great if that works for u. I tried for over a year and have gotten at least 40% worse by listening to those ideas. Last option was avonex, I have realized that there all kinds if levels and Mis diagnosing if ms. I feel that mild cases can be treated more at a natural level , why other cases can not and need to be addressed with an aggressive
Approach. I wish I would of done that route as well as my changes in lifestyle. That is just my experience, it does not work for everyone.