Thanks I will....

The joggers are the Academy guys....Next time you see them it may be in the fall....Toot and give them a hard time.....If its a warm morning and you have your car window open if you see a name on the back of the shirt slow down toot and yell their name.....Within minutes the Drill Sgt will have that person running circles around the crew while the crew is running, while he is singing a cadence song.....I know...My jerk friends did me in quite a few times....
In all seriousness its just funny.....

That is funny! My son LOVES yelling out the window to people. I will have to tell him that one. He gets a kick out of it. He will yell HI or Nice shirt. He yelled FOUR to the mini golf place.

Too bad that was you once!

Hi,
I was told this may be a good forum area to post although I don't have MS, I may have everything else If anyone has a problem with me posting here please speck up...I just know I need human contact and support and I have no one IRL that I can talk to. My nerves are damaged forever, it will only get worse, never better, I have only one sister that believes me and she no longer lives with me due to my obnoxious husband and son. Anyway I am 51 and always feel alone, constant pain, muscles spasms, wake up most nights with my legs drawn up and feel like I have to break them loose. My life stinks!

Hello Junie and welcome to the MS forum

I don't think you find anyone who has a problem with you being on this forum. Although we are a MS forum we get many posting who do not have MS.

Make yourself at home and join in anywhere

Thank you,
I have a feeling I will be needing support tonight since my hubby and 2 of my sons are going to sit outside and drink tonight! I hate drunks! I wish every drop of alcohol would vanish forever!

But not too new to MS.

I'm Sandra know as sw8689 on msworld too. I was dx'd in 2000 when I had my first prevelent attack and within a year lost my career to MS. The beta interferons didn't work for me so I had mitoxantrone and that put me into remission and I have had stable mri's for almost four years now and walk and hike with no problems. Most serious problems are fatigue, bladder, pain and spacticity.

I am looking after my MIL who has dementia right now, she is living with my husband and I, and that has taken up all of my energy and time. And sometimes my smiles.

But otherwise, life is pretty good, I like to garden, hang with grown children, play with my dog, and generally enjoy this beautiful life I have been given.

Thanks Cheryl for hooking me up to this forum! And I look forward to meeting my old friends and making new ones.

Sandra

Hello Sandra and welcome to NeuroTalk.

I'm glad Cheryl pointed you in this direction. Take a look around and jump in anywhere, there is alot to explore here at NeuroTalk.

Sandra found us!! I remember you. I always enjoyed your posts. I hope you have time to spend with us every now and then.

We are in similar situations right now. My grandmother just moved in with us because she is suffering from dementia. It is so sad and hard to watch someone struggle with dementia. There are things that happen that just make me cry because it isn't right that her mind should be taken from her.