My Journey with Multiple Sclerosis

Good morning not sure we’re to start as I said before I’m not much of a blogger or neither will I post pictures but what is ill do is take you on my journey on how and what my ms has been going for me I’m not to much into the lime light giving so much info about myself.many years ago back 2003 I was diagnosed with MS.I was diagnosed in emergency room and I didn’t know I had this disease at the time I could had for maybe way back sometimes but as the doctor in the ER told me you could had this for long time.now that being said as me being a man I guess I really didn’t  care for having the disease or even look into it so I let years pass by with out any one knowing I had this disease.at the time he told me I had lesion in the brain and he told me I should neurologist cause he could help with this so called MS or lesions as they call it.so I never did I never went to see neurologist thinking maybe this would go away and take heed don’t listen to your consciousness do what’s right see neurologist.so about 2007 I started having more problems and I started having vision and walking problems then came the bowl problems then came the stomach problems and one thing lead to another.so I think I saw over 10 doctors in 1 year span not 1 doctor could tell me what was wrong even though they kept saying it was my MS.the most important thing to me is how doctor keep saying it’s MS it’s funny cause when you go the ER that’s the first ring they tell you.I decoded I needed see neurologist and I figure maybe this time around he could help now I had been 2 say 5 them and they all kept telling me fibro or muscle dystrophy or here’s better one ghost pains.so that being said I was left again with no answers none at all still nerve pain and with all the pain in the world I never could be the same again.so on 2009 I went to 1 doctor again a neurologist now I can’t say names but I can see this he is the most I have to say the best neurologist I ever came across I walked to into his office I told my story and he looked at me and said I think we can help you so he said to me I think we have a case of relapsing remittance.he said let do some test so I said sure we did couple and sure enough he said exactly what he thought it would be now he’s colleagues in the other hand thought there wasn’t much evidence to prove it was that bad.this is why the industry is what it is today.doctor all about the money we all know this were a number of everyone.that being said for the 1 year I saw him he had me on copaxone and all the stuff that I needed
Now here’s were it gets better as time went on my body started break down I started getting bladder infections and what they call ic of the bladder and nerogenic bladder and so forth one day my body went into what they called toxicity and my kidneys went into infection and my body couldn’t hold the water anymore I think I was in hospital more ran 20 times that month so I stopped taking The copaxon come find out it was the steroids they had me on.now I’m not gonna throw the doctor under the bus here but I can say he did all he could on the other hand I can speak for his boss. Major DICK! Sorry for that but that how I feel.but I come to find out months later they had let him go now we all know what that means when they let them go so I was back square one again.ah but gets better I finally found him after 8 months so in 8 months I haven’t had anything for my MS in that time I was in worst off ever.here were gets better he’s boss didn’t Wana give me the meds he didn’t think they was gonna help me or even the pain meds he thought was some young junkie here’s what I have to say about all this don’t mess around when comes to your health first and formost we all have pride but your health is the most important thing and if it wasn’t god will I would never found this doctor again.guess what I did and guess what today he’s treating me and I have say him and his staff and done a wonderful job I can say they work with me and I am doing a lot better I can finally use my hands and my feet well I can’t walk like I use to or get out but baby steps.sometimes we let out guard down cause we’re so upset that there isn’t any help but there is and there out there I have a he’ll of team and they have gotten me back on track the one thing I could never get was my wheelchair and guess what they got me my wheelchair and power wheelchair at that why cause being disabled isn’t easy getting around.if your really disabled and can’t move around don’t sit there and let people tell you your life is over. No its not just cause one little thing hinders you doesn’t mean you have to let drag you down.my team is the best in the world and I’m glad I think the main thing is here get checked get moving get motivated and get good team on your side don’t worry about the negatives think about the positives.i hope this helped and I have more to come and I will share more with you on this journey I have a lot health tips and things that could help you get back on track I’m not doctor but I can surely say I’m your friend.

Tecfidera the benefits

Hello I’m not were to start cause I’m new at blogging and this is all new to me the reason why I names maandhealth means Mahealth.but, reason for my blogging is to help people with my story on my journey to Ms medication.year ago I was started on tecfidera medication by my neurologist.I was on copaxon for over 3 years and in that time I really didn’t see a difference in my relapse remittance.I can’t say this for everyone cause I think we all are different when it comes to our MS.now being on this medication tecfidera has given be a better chance to have better days and make me feel little better about myself.now I can’t say the medication will work for everyone but the trials given to me have done well.I still have problems at times with my MS but I think this medication is helping me by far as the best yet.yes there are certain things I have notice with other stuff I have taken like protein peptide powder form and exercise and little bit light weight training and yoga.even though I can’t move and do as much this combination of stuff is making me a lot better and the tecfidera has wonders for me.I can’t say this is the wonder drug but it is most definitely by far one the best medicines I have taken by far.some people ask me what are the downsides to this medication. Well as all meditations there is always gonna be constipation and nuerogenic issues especially with MS.the only thing I have noticed with this medication is that I have more stomach issues than most but my flare ups have been less than ever.I am on journey here for this blog to give insight on what could be good for someone with relapsing MS.I know how hard it can be everyday moving and Doing certain things around the house and getting out bed.but, why does it stop here.why do we have to be disabled or were we can’t be us.theres no answers for MS but the will power we have to maintain our sickness and also choosing the right team of doctors and people around you.i hope this blog will give you lots of insights and help someone I was very shallow about life and sharing my life with people cause I was afraid nobody would care.my doctors and family and support team all care and I will post many blogs on my life and opportunities to help people and let them know there is help and there is hope.