PatientsLikeMe : Multiple Sclerosis Community

Caregiver	My MSer	About Me
notasperfectasyou		My wife has MS. I'd gladly give her my legs if I could. I'm a CPA. If your immediate thought is about accuracy, detail, inflexibly wanting the right answer - that's me. I read medical journals instead of tax court cases now. Kim's had MS for about 20 years. She was RRMS and moved to SPMS about 4 years ago. She's been on Avonex, Copaxone, Novantrone. Kim is now on Combined Antibiotic Protocol and she has recovered previously lost function. We don't accept the word "incurable" and we don't think others have to either. I'm here to share our knowledge of Combined Antibiotic Protocol.
Foreningen Livsnettet
CareJoe
Historian	worthy	I've had the good fortune to be "Worthy's" husband since in 1980. When "Worthy" was totally disabled from a neck injury in 1983, I most willingly became her caregiver also. Since that time, "Worthy" has been diagnosed with Multiple Sclerosis and Fibromyalgia Syndrome and other related illnesses. While "Worthy" and I struggled with limitations imposed by her disabilities, our financial challenges and my own severe health issues, our deep faith in God, combined with our compassion and love for each other, have helped us to find the joys and blessings in each new day.
Rickarou1	mammananny	I am the husband of an MS patient. I was born in Mass. and raised in Arizona. I spent 10 years in the Air force and now reside in Idaho. My wife and family are my life. I am a published author of childrens book and love to write poetry.
maggy63		Our son developed Transverse Myelitis and Multiple Sclerosis at the age of eight.He was told he would always be in a wheelchair and never walk again. His pain was unreal! His story is long, as we searched for years for answers! Determination, and prayers, and God is good. Even all the Drs. asked my husband and I what happened! Johnny is now 18,has been walking almost three years, drives, is a waiter,homeschools,has lots of dreams! One is he is engaged. I was proud to be not only his Mother, but his caregiver for all those years. He is not promised anything, but who among us is?! Maggy63
Abeer		My brother is an MS patient, he is 40 years old and was diagnosed 12 years ago. It's a secondary progressive and now he's on a wheelchair and is suffering from a variety of symptoms including leg stiffness, general fatigue, bladder problems and weakness. He is currently undergoing sessions of a low dose chemotherapy, our last resort according to some doctors to slow down the deterioration process. If you have any recommendation please share with me I'll appreciate it.
ortho
Wolfy288
spacetwink		I am a caregiver and an avocate for probate conservatorship reform. The illegal conservatorships of our loved ones in thier golden years is a terrible injustice created by greety, corrupt and evil probate system. More and more the stories are being told of the abuse in the probate courts allowing people to take over the lives and finances of elderly persons all across our nation. Please help us stop the torture of our elderly loved ones.
paulandpeggy		My husband Paul is 40 yrs old and was just diagnosed with MS in May 2009. He works full time as an Electronic Technician for the USPS Bulk Mail Center.
Erx		My wife got ms dg in 11/2006, she was 31 yrs then. It was nasty surprise and symptoms were quite bad when ms began. Since then I have been studying what is ms and what you can do, to manage with this awful disease. Neurologist said that "just continue your life like before dg". My own "research" led me to diet treatment and since January 2007 we have been with best-bet-diet. And it was very good decicion, cause ms symptoms vanished little by little. The worst symptom in the beginning was fatigue, wife just "stopped". We were happy to notice that fatigue disappeared. Big thanks to Ashton Embry.
InfoHungry
strawberrygirl		Wife, stepmom of 3. Cat lover, homebrewer, music lover. Here to help the man I love
edeme1
ramar	Meehoo	The love of my life was diagnosed with M.S. in 2/08. We have three beautiful children, and two beautiful grandchildren as well as 32 years of love. I know that the road ahead will not be easy, I know that we will be okay!
laskawolf
MS Mom1
sanmeek		My name is Sandi. My daughter was diagnosed with MS at 12 years old. She is currently taking Betaseron and CellCept for her meds. We have been doing great for almost 22 months. She is currently 15 years old, and is a very active girl. She just recently started playing softball, and High School.
grayling		I'm 56 yrs old wife has secondary progressive in a wheel chair left side not useable.

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