Tag Archives: Income tax

Busy Day Yesterday & Today

Day by Day with a Movement Disorder Posted on by 2

We were very lucky to find a Walmart that actually had the Acai on the shelf. Since it has become the new diet craze to use Acai with a Colon Cleansing routine it’s been hard to find. I think I can thank Oprah for that. LOL!

Anyway, since we now have a 6 month supply on hand I don’t mind taking 4 gel caps of it a day. I am going back to eating a little something when I take it, though, until I’m sure that it doesn’t irritate my stomach lining.

We were also able to buy 5 bottles of MiraLax at CVS for a considerably reduced cost, which will be 2 1/2 months worth for me. That is actually the most expensive medicine I’m taking now. It was much cheaper for me when it was a prescription, as my insurance was picking up a large part of the bill, but I’m sure there are a lot of people benefiting from it, now that it is OTC.

I had my yearly appointment with the Dermatologist yesterday, which went quite well. It makes me very nervous, and the stress is not good for me. But he found nothing suspicious. He has prescribed Aclovate ointment for my severely dry skin and a few patches of what he called eczema. All I could think of was great … another prescription. But I will fill it and use it sparingly on the worst places. I’m leary of using too much at a time, because it is a steroidal suspension. I have learned to be very cautious about steroid meds since my horrible reaction to Celestone when I was on PD meds.

So, first thing I did today was to do a drug check to see what the side effects and warnings were, and also to check for drug interactions. It came back OK on the drug interactions, and the cautions had to do with thickly applied ointment, particularly if it were bandaged. I won’t be doing that, so I should do just find on it.

We hit three different Thrift Stores while we were using the gas mileage and found quite a few nice lovies to add to our Plush Animals Shoppe catalog. Of course I can’t wiggle my nose and get them online, but I’m making progress slowly to get our inventory online.

I continue to do my morning exercises, and managed to do three sets today, using the 3.5 pound weights for the last set. I also used the trekking poles to walk around the house a few times this morning and stayed on the mini trampoline for 20 minutes. I’m really pleased with my improvement on the exercises, but I am not yet seeing it translate to a more fluid gait. Patience … patience.

We spent some time today trying to get all the business paperwork together in preparation for doing our taxes. That’s one chore I still do, because I am used to the TaxCut software. Hubby’s made tremendous progress this last few months in his use of the computer, but taxes would be a little too much for this year. By next year, if I need to turn it over to him, I feel sure he will be able to do it quite well. Hopefully I can continue to do this, as it’s a good way to keep my mind sharp and also keeps me aware of where I money is going. This last year was the first year of our married lives where hubby took care of all the bills all year long.

Add in a few posts to the Lost Toys Search Service, and it turned into a very productive day. Now today I’m getting ready to take a bunch of photos to start on another page of our Shoppe catalog.

I’m proud of my efforts and increased activity level, and look forward to improved health.

Been to the Physiatrist and I’m Still Very Busy

Day by Day with a Movement Disorder Posted on by 9

I saw the Physiatrist yesterday. He’s the doctor who had to review my records before he would agree to even see me. As it turns out, oddly enough, he is the person who did my original EMG and Nerve Velocity Tests.

I was extremely pleased that he did a complete checkup, rather than just asking about my neck. He went through a complete neurological exam, but didn’t venture much as to what he thought was wrong, other than to say Dr. Watts was the one who would be able to say what is going on. He did say he was sure I had some kind of Movement Disorder, but he didn’t think it was Parkinson’s, either.

He went over some options for the neck pain that has persisted since November. We agreed to try the least possible first, particularly since I will see Dr. Watts in less than three weeks. It’s hard to imagine that something I’ve waited so long for is almost here! Anyway, the Physiatrist gave me a prescription for Lidoderm patches that I cut and apply to the trigger points of this pain. They are basically Novacaine that goes through the skin to the muscle. He felt like I would not have any stomach problems by doing it that way.

I put half on the top of my shoulder near the neck and the other half just below the shoulder blade, next to the spine. Those are the spots that really scream if I sit or stand unsupported for very long. Even the time to wash a full sink of dishes or eat a meal at the table is usually enough to set it off, and sitting on the church pews has been very uncomfortable.

I felt a little bit light headed soon after putting the patch on, but that could have been for any number of reasons, as I had not eaten breakfast yet. I am hurting now, but maybe not as bad as usual. Obviously, one day’s use can’t calm down this spasm, so I will just have to see how I do. The prescription is for 3 months worth, and thank goodness I have Medicare and good insurance, as it was listed at over $500!

I’ve been going around in circles lately trying to get a whole lot of things accomplished all at once, and not getting much finished at all. We have started on our taxes, but there are some parts that I must work on before the exact number can go in the form. I’ve been doing them with software for years, but this time my hubby sat down next to me and we went over each part together. That helped me stay calm, plus he needs to know how it’s done.

I’m also trying really hard to get as many of our toys in our online catalog as I possibly can, and I have run into several road blocks I had not anticipated. I had to learn how to use a Shopping Cart program, upload and download files to Google and our ISP to make a searchable data base, and I have been driven half crazy trying to get the catalog to show up properly in Google Base. OK, I know if you are not using the programs yourself that was just a bunch of gobbledygook – but they were very confusing to me, too, and I am definitely not learning new things as quickly as I once did.

I’ve had printer problems and had to buy a new one yesterday, so I couldn’t mail out some orders today, because I hadn’t figured out how to set up the network part of it. That actually worked pretty well, once I did understand the directions, and it even has an answering machine and fax included in it! I feel like I have my own home office now.

Our Search Service is keeping me extremely busy, too, and we have made a few sales from it, as well as helping several very happy parents find the lovie they needed, whether we made the sale or someone else did. I am pretty much caught up with answering the initial request, but I am miserably behind at getting the ones I could not find turned into blog posts.

I feel bad about that, as some of these parents sound so desperate, but hubby is still computer phobic, and that leaves this part of the business entirely up to me. He’s great at scouring the yard sales and thrift stores several times a week when he goes out on his own, and we thoroughly enjoy our Friday Date Day, and he helps a lot with the packing. He takes everything to the Post Office, too, and he has a lot of input about how to do the business side of selling. He just doesn’t want anything to do with the computer part.

Well, enough about all that. It just goes to show that I am staying busy with lots of different parts of my life – and our messy house proves it. Something had to give – so…..

Hopefully it won’t be so long before I post again.

Re-Testing Peripheral Neuropathy Monday

Day by Day with a Movement Disorder Posted on by  

I see the MDS specialist the first week of April, so it seemed like a good idea to ask for a Neuropathy test before I see him. When I first saw my Neurologist, it was at the suggestion of my Orthopedist, who had concluded that my super labored walking was not caused by lumbar disk pressure.

He sent me to Lakeshore to have the Nerve Conduction Velocity Test, which uses patches like those they stick on the chest to check for heart problems. They pass an electric current and check to see how long it takes the message to register between the patches. It’s uncomfortable at the time, but not really too bad. The other test is called Electromyography. That’s the one where they poke electrodes the size of needles in your muscles, and it is supposed to show how well the muscles respond when the nerve is stimulated. That test is not at all comfortable. I actually had little pin prick size blood spots all over my legs when that one was over.

Anyway, the results showed definite Axonal Peripheral Neuropathy, mostly in my right leg. Because I was having trouble walking, and the test order came as a result of my Ortho dealing with my back and legs, he did not order the test to be done on my arms as well.

My Neuro was not at all happy that he did not have results for my arms as well as my legs, but he proceeded with the info he had, as my insurance would not likely have paid for a repeat test so soon.

So, I talked to his nurse a couple of days ago, and I’m scheduled to have the complete PN test battery Monday, at my “suggestion” – translate that as strong urging. This test is very uncomfortable, but it seems to me I need to get any tests done now, not wait and “waste” the visit with this very hard to see Head of Neurology at UAB.

I’m still experimenting with any variables I can think of. so, for the last four days I have not used the TAP dental device, which is to control my mild Sleep Apnea. The mouth tics started about the same time I started using the TAP, and I’m trying to be sure that this off and on again mouth twitching I’ve been doing is not being aggravated by the mouthpiece. Surprisingly, I’m still sleeping 7 or 8 hours a night, even without it. I think it did break me of the mouth breathing habit, which may be the cause of the relaxed jaw that was allowing my throat to close up during sleep.

I have noticed a definite correlation between the mouth twitches or tics and how stressed or tired I am. So they get worse as the day goes on. If I stop to think about them, I can stop them momentarily, but it’s as if my mouth is determined to move, no matter what I do, and it soon starts back up again.

I figure I’ll make sure Monday that there aren’t any other tests I should have done, or repeat, before seeing Dr. Watts at UAB. I have to call his office to change my insurance information to show that Medicare is my Primary insurance now, as this is the month I turn 65. So I will talk to his nurse and see if they suggest any other tests. I have learned to be proactive in such situations. It amazes me that doctor’s offices don’t initiate this kind of pre-visit planning, but they don’t.

By way of contrast, when we made an appointment with a financial counselor to help us with investing my inheritance, we received a huge packet of papers to fill out and a long list of documents to bring with us for our first meeting. That’s the way it should be with doctors, in my opinion.

So, I will do what I can to document everything and have everything ready for this crucial visit. I can’t even talk to someone about Long Term Care insurance, or anything insurance related, until I have a diagnosis. No insurance company in their right mind would take me on as a customer right now.

Tax Time is looming, and that’s one thing I am dreading doing, but I can’t put it off much longer. Oh, did you know that people who file an extension will NOT receive this stimulus package $300 thingy they all keep talking about? I have always filed on time, but I know some people habitually delay it, and might need to know that.

I continue to work to get our inventory of plush lovies online, and we have managed to help several families get replacements for lost toys lately, which is extremely satisfying. I’m also helping to beta test a new Mood community on Patients Like Me, and finding the charting of my own moods to be interesting.

I may be twitching, but I am in a good mood today, and that’s a great way to end this post.

Messing Around

Day by Day with a Movement Disorder Posted on by 4

Well, I went to the Dermatologist Monday, and other than a small flareup of my Acne Rosacea, he didn’t find anything worrisome. He did say I had some sun damage on my forearms … But I’ve had almost 65 years to accumulate that damage, so it’s not really surprising. I did the sunbathing stuff in high school and college, but that’s just about it. I did have some pretty bad sunburns during that time period. Of course, there were no sunscreens then.

I’m finding the cervical collar to be very helpful, but it hurts to wear it. I’ve made about all the adjustments that I can to make it work better on my short neck, but it is still uncomfortable. Let’s face it — I have a small face and CPAP and Collars were just not meant for someone my size. It’s a shame my hips and tummy haven’t figured out they are supposed to be petite, too! LOL

I’m not getting as much use from the TEN’s as I thought I would, because it’s trouble to hook it all up. That old apathy thing going on again. I need to get in the habit of putting it on before I eat lunch or ride in the car. Those seem to be my worst triggers for pain. It’s the leaning forward with no support posture that makes mealtimes hurt. For breakfast and supper, I’m usually on the computer on the sofa, with the laptop in my lap, eating in between typing. Yes, my keyboard needs cleaning out something terrible, but I don’t know how.

I’ll try to do better by the TEN’s today. It’s rented for one month, and then, if I think it helped, insurance will pay for it. Seems fair enough to me.

I got just plain disgusted the other day, and told hubby I’m going to go off of all my PD meds for awhile, just to see how I do. I made a short experiment with that right around Christmas, but the holidays weren’t really a good time to be experimenting, so it was a very, very short time that I was without the meds. I intend to stick this out for at least a week, maybe longer. I just want to see once and for all if the meds are doing me any good at all.

I worked hard all day yesterday getting more of our plush animals and dolls into our own Dirty Butter Plush Animal Shoppe, so I can more easily sell directly. I’ll still be on eBay, but I need to wean away from depending on that source completely for sales. EBay messes with things too much, and changes things at a whim. At least with my own site, I know exactly what’s going on. Course, right now, not much IS going on!

I started working on tax forms I have to fill out for the paid caregiver we had with Daddy. Once I do all his taxes, and the Estate’s taxes, and pay what is owed to the IRS, we can close out the Estate bank account, and invest the money. It will be good to see the end of that chapter of my life.

Hubby continues to be supportive and helpful, I feel better, I don’t have any signs of skin cancers, and I’m accomplishing something with our sales. I’d say that’s a pretty good sign that the apathy is lifting. I sure hope so.

Getting Back to Normal?

Day by Day with a Movement Disorder Posted on by 6

I’ve gotten a lot done in the last few days. We’ve had the appraiser out to the house, the taxes are ready to sign and mail, and I’m almost finished with the tax bookwork for our paid caregiver. I finally gave up and went to the Orthopedist about my knee and shoulder, too. The X-rays showed the degenerated cervical disk I already knew about, and arthritis in my knee, which wasn’t surprising. Dr. J is guessing that I have a torn miniscus, but it will take an MRI to determine that. From what I’ve been able to read on the Internet, that seems like a reasonable diagnosis to me, particularly since it was injured when I was shifting Daddy up in the bed.

I’ll have to go to Physical Therapy and stay on Extra Strength Tylenol 3 times a day before my insurance will agree to the MRI. That’s fine with me, as far as the therapy goes, as I’m sure it will be helpful. The Tylenol doesn’t even faze the pain, but I’m following his directions and taking it regularly.

We’re still walking at the track early in the mornings, but it’s been way too cold the last few days. Alabama is having record cold weather right now. So, we’ve been doing exercises from videos. DH is REALLY following the tape, and I’m bouncing on one of those little trampolines and doing as much of the arm movements as my shoulder will let me.

I’m still just taking the Zelepar, hoping that the exercise and whatever the doctor does for my knee will be enough. I just don’t want to try the Requip, if I can possibly help it.

We had our usual Date Day Friday and enjoyed looking at lots of Estate Sales. We’ve never been able to be an Early Bird before! It was strange to get there before most of the stuff was gone. And we did manage to pick up a few good buys, I think.

It’s been ages now since I’ve taken pictures and put anything on eBay, but I’m going to try to get back to that this week. We have an almost overwhelming amount of “stuff” we’ve bought in the last few years, and I haven’t been able to work seriously on our online sales for almost 2 years. With so much of the Estate business started now, I’m ready to get back to NORMAL.

Lots to Do Settling Daddy’s Estate

Day by Day with a Movement Disorder Posted on by 12

This is the second time I’ve been the executor of an estate, but Daddy’s is much more involved than Pop’s was. Luckily, we have a niece who is a lawyer, so I’ll have some help when I’m ready. I’ve tried researching what I need to do on the Internet, and I’ve been surprised at how little help I could find. Everything seems to be geared toward Estate Planning, rather than settling an estate.

April 15th is getting closer, too, and I’ve just not been up to dealing with important numbers. I did get a good start today, though. Starting is half the battle for me, as I find I’ve become quite the procrastinator in the last few years. I don’t know if that’s a sign of old age LOL, stress, or Parkinson’s!

We walked again this morning, but I was slow as mud. I made it around for a half mile, using the walker. I’ve been using the walker all this week, but I depended on it more today, as I could feel the tightness in my shoulders when I stopped. That slow as mud feeling is the first Parkinson’s symptom I had, so it’s looking less and less like I’ll be able to continue on just the Zelepar. The Neurologist told me I could go back on the Requip as well, if I felt like I had to. I’ve resisted, because the Requip gave me stomach troubles last time. Well, I had stomach trouble when I was on the Requip – that doesn’t automatically mean the Requip was causing it. It’s that uncertainty that has kept me trying to do without it. I’m just not ready to cope with stomach side effects yet. Maybe next week.

I taught 4th and 5th graders for 25 years, but I’ve seen the “Smarter than a Fifth Grader” TV show a couple of times since I’ve been back home. It’s scary how much my mind goes blank on stuff I know I should know. I hope it’s just remnants of caregiver burnout, and not the PD effecting my mental abilities. Stress can really do a number on such tasks, so I’m trying really hard to relax as much as I can. But getting things accomplished is part of what’s needed to lower my stress level, too, so it’s a matter of finding a balance, I guess.

I continue to be uplifted by all the loving comments. You all really are helping. Just a thought for you, if you need to send a sympathy card to someone. One of our friends included a neatly cut out copy of Daddy’s Obituary notice in their card. It was very much appreciated.