bebe
bebe
Sex: F
Data Quality: 2 stars
MS: 15 yrs
Type: Relapsing-Remitting
Sensation: Moderate
Overall: Mild
Cognition: moderate
Vision: moderate
Speech: moderate
Swallowing: mild
Upper limb: moderate
Walking: mild
bebe
Female, 60 years
Carencro, LA
Primary Condition
MS
Type
Relapsing-Remitting
First symptom
Jan 1997
Diagnosis
Feb 2008

About bebe

My husband and I love to camp with our three babies...two standard poodles and one very old boxer! We have a small organic garden and lots of fruit trees, as you have guessed I really love to be outdoors, which is a real challenge in south Louisiana heat! We have a large family with lots of grand-babies and I have one sister who lives in Birmingham, Al. she is an occupational therapist, and has been able to help me a lot. My Mother is well and strong and lives in our area. My support group is wonderful, I am very lucky. I am newly diagnosed with M.S.

Profile Activity
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Member since: Mar 08, 2008 Last Login Mar 29, 2012

More About bebe

Cool I have had strange symptoms for many years.  About 16 years ago I had bells palsey,  after that I sort of noticed that I felt tired a lot,  and didn't really have much energy some of the time.  A few years later,  I noticed I got very sick when I cut our grass (which I loved to do) I thought that maybe it was allergies (never thought of the heat).  Slowly things went wrong,  I became lactose intolrable,  had stomach and bowel problems,  a hot pain between my shoulder blades that never went away!  My legs from my knees down began burning when I stood up too long,  or walked too much.  But,  really things have gotten worse,  bad enough to seek medical advice in the last in about the last 7 or 8 years.  My internist dismissed the symptoms,  and I just thought I was complaining too much.  Finally it got too terrible,  my eyes were giving trouble, I was exhausted all the time,  if I got overheated I began tripping, legs hurt more,  everything worse.  It wasn't until I began having pins and needles in my legs,  and numbness around my mouth did I get a refferal to a neuro who did a M.S. workup,  everything was pretty normal except my brain MRI had 13 leisons.  She then sent me to Houston to see Dr. Rivera, a M.S. Specialists.  He confimed the dx just 10 days ago.  I am still not sure what meds I will or will not be on.  I am coming to terms with it all,  and looking back now realize that I have had M.S. for a long time...I have been very lucky to have what seems to be a very slow progressing disease,  I guess time will tell.  I will try to live one day at a time and not worry what might happen,  I have a lot to be grateful for.