ILL TRY TO REMBER THAT AND ILL TYPE IN ALL CAPS WILL THAT HELP
Good morning melissa,
I am so sorry to hear you day is starting out rough (to put it mildly). I hope you will hang in here with us - we're good listeners and actually share some laughs too!
Can you do us a favor and try to break up your posts into short paragraphs? Many of us have vision problems and it is very difficult to read long paragraphs such as yours.
Truthfully, we often give up on reading what has been written if it gets lengthy because the words all blur together! Yes, another fun MS side effect. :-)
Here's to a good Friday for you - I hope it improves.
my best,
Lulu
i dont know why i have to take the test again the firt test i took was the phyc test it was like ging to take you GED i passed that one so i gess they thought i was to fit to get disability so i apilled it and got a free lawyer and now i have to go do a physical examination on the 18th of this month i pray i get in to see the new nero and get another supportave MS evidence and this time they give me the ok for disability if not i dont know what i will do i cant go back to work my body cant take it so i will be doing aloy of praying in answer to the letter from my last nero in morgantown she wont rule me as haveing MS so on to the new nero that realy dose know what MS is and says i have it (not that i want MS but at this point something has to give before i go crazy and snap from frustation) if you know what i mean i look healthy on the out side but people only see me out and about on good days they dont live with me or see me fall down stairs not being able to pick up my baby do to arm and hand weekness cutting myself when cooking cause i cant feel my fingers or any of the other thing that are wrong with my body do the my MS i waer pads or depends all the time so i dont pee myself now which is so imbaerasing im only 35 years old people just dont understand what we go through each and every day the pain the degrading stuff we have to put up with the laughing from steanger when u fall out i public and have to crawl to something so u can pull yourself up to stand and pray ur leggs can get u out of there ASP they dont see u at night crying ur head off or the panic u feel over waking up and thinking is this the day last day ill be moble well better spend it with care and love do happy thing (memberalthings) with my girls before i cant move at all all that people see i the happy face that u paste on every day till u feel like its going to crak sorry for venting and going down the dark thoughts this morrning woke up wet and lifeless legs today so im off to a great stare lol
Hi, glad you reported on your doctor visit. I thought you might be needing the assistance of the "system", which is why I offered the support in my last post. If you haven't seen that, it's in answer to your previous post. I'm curious as to why you have to pass a residual function test in person. What have you done thus far to apply for disability? Obviously you need a doctor as an ally. That's why I suggested that you send for a letter from your previous doctor. Is that possible? Also letters from people other than relatives who are familiar with your limitations can be a benefit. If you'd like more info, PM me and I'm be glad to offer some insights.
I wish you the best, Jan
Hi
I am glad you came to this site, Its just wonderful here
Wishing you the best to get the help you need Linda
Good evening Melissa,
Its good to hear that you got a referral to a different neuro.
Here's hoping you get back on track with the MS diagnosis and get help.
keep us posted, ok?
Lulu