| Our MS Space Living with MS Stories, Poems, Struggles, etc... Living with MS |
| My name is Gina and I am from Alaska. I was diagnosed December 31, 2007 with RRMS. I have been having problems with my knee giving out and know that a Cane might help me in the near future. I was kind of reluctant because I am only 31, until I saw your wonderful creations. I Googled canes and found your site. I know when the time comes I will for sure order from you!!! Thank you for being so PRO ACTIVE!!!! I found wonderful support on MSWORLD.ORG and have received lot's of information. Until then take care and thank you! Gina Anchorage, Alaska Betaseron, 1/1/08 |
| Hello, My name is Rita, I am 57 years old, married 39 years, have one daughter that is 35 and I was diagnosed with MS in October of 1979. I do well other then I use a wheelchair. I am STILL Me I am just a lot slower and shorter..haha....anyway, here is a picture of me. We live in Ohio and we are AVID Ohio State football fans. Lets get the word out, we need a cure...:)...I take daily injections of Copaxone, have a Baclofen pump for spasms. Lets beat this Monster.:) Thanks, Rita |
| Hi My name is Michelle i live in the small town of Mexico, Maine. I was diagnoised with MS last Feb. i have been having symptoms for 4 years before i was diagnoised. i am the mother of 4 great kids. i to feel left behind do to this illness. i am so tired all the time. I am glad that my Husband is so supportive. he realy got more then he bargined for. i think that the hardest thing is being 30 and on my bad days i feel like i am 60. I am lucky i have found a job that they are very understanding. i work as a team leader for a socail services company. we work with a wide varity of people.i love it, i love helping people but i find that i never take the time to help me. i guess it is if i don't address it then it is not there. i know that this is denial but sometime i can't get out of the poor me thing and i hate that. anyway thanks for the small chance to vent...lol not to many people want to hear it you know. i always say i have the disorder no one believes because you can't always see the sffects. |
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| My Daily Blog about living Day to Day with MS. I have been told for years that my life is more entertaining than a Soap Opera. So even though we all live with MS everyday not always is that what is going on in our lives. This is a daily journal of my life and thoughts for the moment or day. There will also be information that I might find and want to get out to the world about MS. Stop by and take a look and subscribe to it. This will make keeping up with the blog easier for you. |