hello everyone, I'm a senor women...nope I haven't really been told I had MS yet. I have a lot of the things going on that looks like MS besides several other types of dieases.
I had now up today 4 TIA's including one last night...I was in the hospital for 4 days up to last Monday. Where when I was let go the doctor gave me copies of the tests. When I got home I started to read them....mostly normal and some not so normal. But the one world on my CT enlighten (it's what I call it when they use Iodine) anyway It had this very large word microaniopathic ischemic disease in their final report. I could tell you they saw another large size Lacunar Infarot from a few years ago...they also I'm leaving out a lot sorry, but the low-density priventricular changes suspicious for: (that big word). I know backwards.
I can tell you all I saw a Neuro doctor last year when I was not as bad as this year...he did EMG and tons of MRI's on me. I never heard of Lime diseae until reading here.
He said I had serve sensory Polyneuropathy....so I wanted another opion...and earlier this year went to Barrows Neuro. Hospital, MDA clinic here in Phx, AZ. They did another EMG and most of it was normal but only would look at one leg, my left left, by the way I have drop foot on the left foot. When it came time for the Pins...They told me that I don't kick in the miscels. I had sorry i forgot what it was but it was a term for all muscel dieases. I do having memory lost a little lately. I 'm 64 as of June this year...thank you.
But I fall a lot...what is weird is I am all over the place with numbness, weakness, and my body doesn't follow right things for them LOL I think it's LOL. Anyway I am getting worse lately.
I had medicade up until earlier this year, and now since my medicade kick in I am on unitedhealth care plan...Lets see yes, I have a heart stent in LAD, I have COPD, and I have something else besides all these problems of walking right. I forgot again. But I am getting some in home help right now...for a while....I have life aleark the state gave it to me for falling down...I never know sometimes when I will fall...and I do sometimes with the pain. I have only one pine pill since I have to find a new Neuro doctor...beleive it the doctors don't always take your insurances...so I don't have real help so I go to ER a lot....they saw me last night now I have to stay on blood thinners problably rest of my life...they couldn't tell me....I am trying so hard really. when my eyes don't see once in a while...or lately. When I can't walk one day then the next I can...when I just feel so down...well I know that I just now from the hospital am getting a Neuro doctor...yeah...maybe I will know what is really wrong with my body. sorry i might of forgotton all I go thru...but its a daily thing.
thank you for letting me write here...oh I have something going on with my hands at least one likes to move a lot...my husband hates it. thank you