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About Me
emarmolejos
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About Me
Everything is changing.
Everything is changing.
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Interests
My God, my family, my friends...oh yeah and ANYTHING THAT INCLUDES HOT GLUE, A SEWING MACHINE, FABRIC OR A CAMERA! I love arts & crafts. I also love taking pictures!
My God, my family, my friends...oh yeah and ANYTHING THAT INCLUDES HOT GLUE, A SEWING MACHINE, FABRIC
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Recent Activity
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Journal
This entry is private
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Hugbook
Hug
Fine looking family there.... sorry about the MS... You shoulr find support and friendship here... take care... Clare
Flower
i think maybe you are taking too much on at one time. a few weeks or months is not enough to fully understand that you have MS. i am less than a year knowing and i still break down and cry and cry for days and days. then i recover and it gets less and less. you are still young, and it is very difficult to know this is going to cover you so long. and as far is shared solutions is concerned, their calls can drive you crazy. all they want is that you are taking the meds so they can get their quote or commission or whatever or the number of calls they make. i had to ask them to stop calling several, several times. do not worry, you are not having a pity party, and even if you were you are allowed to have them. do not gang up on yourself. my best to you.. twinks
Hug
maybe your body is telling you copaxone is not for you. Have you looked at low dose naltrexone?
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I have my licence, 'got it in 1985. Not able to do hair anymore, but I stopped doing hair for other reasons only 2 years after getting my licence. However I am unable to do my families hair anymore. But this took years before I had to quit. The funny thing is, my husband is in need of a haircut and doesn't know that I've quit doing even that!
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Hope you are doing well
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Photos
emarmolejos hasn’t uploaded any photos yet
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Support Groups
Close Multiple Sclerosis (MS)
Woke up on 9/7/08 & couldn't move my left eye. Horrible! I could drive, I couldn't read more than 10 minutes without getting a headache. It lasted for 1 month. I live in Arizona and coincidently I experienced slurred speech, tingling and in my face all summer long. It wasn't until my eye tripped out that my husband INNSISTED that my doctor order an MRI. Sure enough there were lesions in the parietal lobe of my brain. That's my story!
Treatments
- Copaxone Too Soon to Tell
- Waiting to get my medication in the mail.
Close ADHD / ADD
emarmolejos hasn’t entered any details for this support group.Open Child Support & Custody
I have joint physical and legal custody of my 6 year old son. I can't leave the state w.my son w/out his or the court's OK & vice versa. I was recently diagnosed with Multiple Sclerosis and the summers here in AZ are murder on my symptoms. I may need to move out of AZ eventually, but I'm not sure how that will work with my joint custody. I don't want to leave my son nor do I want to take him away from his dad.
Open Myasthenia Gravis
I was misgiagnosed. I was diagnosed with MS, but my doctor was torn on my diagnosis when he made it. He was torn between MS & MG. So, he went with MS. Nothing that I have gone through since my diagnosis have been in line with MS. Not that there is really a line that MS follows, but the symptoms have not been consistant wit MS.
