Wait, what day is it?

Have you had one of those weeks?
We have.
When it feels like it should be Friday and it's only Monday?

or It feels like a Monday but it's Wednesday?

What through us so off is lack of sleep and anxiety over Joe's Appointments on Tuesday. They went so well! 1st was his Physical Therapy Appointment, we did it there in Spokane because they have a Multiple Sclerosis specializing Therapist there. And if she was to decide he needs weekly visits or something we would follow up locally. But she diagnosed Joe as a Spaz (his words not mine). Joe has Spasticity in his legs, it is what is making it hard for him to walk lately, especially after this last flare up. Basically it means that the muscles in his legs are tight and cause spasms and it can make the muscles feel stiff. Joe is in the middle in the scale they rate him, so not so good but not so bad either. (for more info go here) He has been given a list (with pictures) of stretches he needs to do at least twice a day, and he should try riding a bike too to loosen up those muscles (and Dad has already set him up a bike on the trainer and he is ready to go, after he did that they talked about really getting Joe ready for a cycling event or something?! boys!?)

Next was lunch of course, got to feed my boy... then the MRI. I love how close everything is, the MS Clinic it technically an extension of Holy Family Hospital in Spokane, and Inland Imaging is in the hospital itself. I really enjoyed the guy that helped Joe get ready for the MRI, he was young and has a great attitude for the kind of work he does (he had just met Dr Cooke that day!) After he was set we left him with a phone and walked around (otherwise I'd be going nuts waiting, it takes a while you know). Joe said the MRI went well (as well as you can expect being put into a tube of magnets that buzzes and bangs- you should hear his impression of it..lol)

Joe will be in to see Dr. Cooke again on Nov 30th (not soon enough, but soon enough, he's hard to get into) At that appointment we should be making the decisions on medications and getting then started ASAP!! And we will be so on top of that. He has waited long enough, but we do understand that the MRI had to come first and that because the previous Neurologist didn't give Dr Cooke the requested info (Grr..) Joe was re-diagnosed with MS, which sounds weird but it's good, they agree and Dr Cooke didn't need to see what another Dr had to say he did his own tests and came to *almost* the same conclusion.

What astounds me is how often we have heard Dr Cooke and staff ask why, why hasn't this been brought up before? Why didn't you know he had Spasticity? Why haven't you seen a physical therapist before for MS? Why didn't they MRI your spine? We would like to know that as well, but we are still grateful for the care and treatment that he received with his last Doctor, he saved my husbands life. Before he was my husband, and now Dr. Cooke is saving his quality of life and giving us the resources to do everything that Joe needs.

I love my husband Joseph, he is more than worth all the hassle it is to take care of MS. He is my miracle and my example he is so strong and brave and I will stand next to him through whatever else life has to through at us.

-S

P.S.
more to come it has been a seriously weird week. :)