2006-10-17 16:27:09 · 10 answers · asked by susie_notts 1 in Health ➔ Alternative Medicine
Hey there,
I was diagnosed when I was 19. I am now 46 and on top of my game. I still walk, dance, just enjoy life. Yes there are days I have to take care and rest. I have had 2 major attacks in 27 years. Yes I have been in a wheelchair, walk with a limp, looked like I had a stroke on my left side, bedridden, shakes, double vision and I could go on yet I don't have to. you get the picture. I MAKE my brain fight everyday so I will not succumb to the disease. I realize there may come a time when my brain will get tired. However, in the mean time, I live each day to the fullest and have fun with life. Life only goes around once, it isn't a dress rehersal. Yes, I have my days that I am depressed and angry. I somehow have the ability to snap out of it with the help of cannibus. Make sure you take care of yourself too. I still have a nagging notion in back of my mind, I need to keep proving myself. I can still do things and nobody is going to tell me I can't.
I was in denile for about 8 years when I was younger, and that sucked. I finally approached MS head on and fought for a life I could enjoy and my independance. I keep my Spirit close and appreciate the gifts I receive which are many. The bottom line, I can still walk on my own and dance a jig. Partying is the best., and playing pool(billards). I, too, went through the "poor me syndrome" and that only get's a person whimpy. Like I always say: my sympathy is between **** and syphilus. I look at life with humor and entertainment. I do believe with my attitude makes me as well as I am.
O'hock
2006-10-17 17:23:50 · answer #1 · answered by orcahock 3 · 0⤊ 0⤋
I am sorry for whomever has this disease. While I dont have it; my husband was checked for MS and a host of not good things (Guillan Barre, MD, etc etc). What they did find was another autoimmune disease: anticardiolipid antibody syndrome (APS or Hughes syndrome). This was devastating news to digest and we didnt understand it well. MY bosses wife is a Dr w/ MS at Childrens Hospital. He had her call me and she explained that w/ news like this you have to go thru a grieving process since you have to accept that there is no cure; just management. ONce i realized this and we let ourselves grieve and eventually accept it, we are and have been fine.
Again, we havent experienced MS but an autoimmune disease (that presents as MS) as well. I would read all I could and keep up on all the advances that the medical community makes.
Good luck and God bless!
2006-10-17 23:40:13 · answer #2 · answered by debberu 3 · 0⤊ 0⤋
Avoid all toxic exposures (food additives,cleaners, personal care products,environmental Etc.) Avoid aspartame and artificial sweetners. Add flax seed oil, fish oils, olive oil, omega 3 oils,etc. to diet. Avoid all hydrodgenated and trans fats. Avoid sugar and simple carbs I decided to try the natural root instead of going on prescription medicine my doctor was against this at first he monitored me carefully though. I started taking, vitamin supplements such as protein, co enzyme Q10, Omega 3,B-Complex,Vitamin C, Alfalfa, Optiflora, Nutriferon, Cal Mag. I took all these vitamins because my case was quite serious. Since you have just been diagnosed with MS I would maybe start out with Alfalfa, Coenzyme Q-10 and Omega 3 first and see how you do.
2006-10-18 00:25:45 · answer #3 · answered by Anonymous · 0⤊ 0⤋
Sorry to here of your plight. In the short term- no can't be of too much help. However, have long term knowledge and experience of the UK benefit system and if/or when you need to consider Incapacity or Disability Benefits - can (a) assist you completing the necessary claim forms and providing advice on how to go about things.
If you need more specific advice of a personal nature - then email me: - geoff.chaplin@btinternet.com
2006-10-18 01:34:20 · answer #4 · answered by ? 5 · 0⤊ 0⤋
I'm a nurse who has cared for many people with MS. Seeing people in many "stages" and progression of the disease is helpful when I say be prepared. I was shocked and amazed most time and the level of self-care my patients administered. Some could do anything with very little assistance, ie: toileting, dressing, undressing, transfering. I was amazed, acceptance and preperation is on your side.
2006-10-18 01:08:45 · answer #5 · answered by kevin j 1 · 0⤊ 0⤋
Their is a lot of help out there. Get what you are entitled to.
My sister has had MS for the last 5 years, and if it wasn't for my parents, I'd just hate to think what would have happened to her.
Unfortunately she has the aggressive form of MS.
All i can advise you is to be their for your friend and stay strong. If in doubt about anything ASK ASK ASK.
2006-10-18 03:33:42 · answer #6 · answered by classychick 2 · 0⤊ 0⤋
Look up Colamine on the internet (Calcium AEP)
See also Prescription For Natural Cures for a load of good advice and info.
2006-10-19 20:27:27 · answer #7 · answered by Mad Roy 6 · 0⤊ 0⤋
yeah try changing your eating habits and it might cure the MS... read the book below or check out the website... proven to help cure all illnesses and diseases...
2006-10-17 23:40:58 · answer #8 · answered by Anonymous · 0⤊ 0⤋
get all the imformation you can try and find a support group and take one day at a time Take Care and Good Luck
2006-10-17 23:50:19 · answer #9 · answered by Nicky T 2 · 0⤊ 0⤋
what you have a Massive Stick wow
2006-10-18 00:06:23 · answer #10 · answered by Midnightdragon 1 · 0⤊ 0⤋