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Red I hope you recover soon an the idea of the bidet is great-I am sure most elders would find this helpful.
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The reddish blotches can be from blood thinner or as we age, our skin becomes thinner & we can burse from just a pinch....Aspirin can also cause it, as it is a blood thinner too. I am a R.N. & if there is only one patch to see on his arm, I would not be worried either. If your concern's mount, take a pen & outline the spot & see if it fades or gets darker or larger....I believe this will help you to know that he is ok or to report it to the AL home. Happy Holidays...
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hi everyone I have been following the Missing Jim blog for quite some time now, Jim has early onset Alzheimer's- although my husband (83) does not fit into the early group, the symptoms and stress is the same, even a bit more difficult being a working wife with two young children - they have just opened their doors to help all caregivers..starting with help with elder care attorneys, respite care for caregivers and Make a Memory family vacations, she has taken our words to Capitol Hill hopefully we can help her bring Alzheimers to the forefront
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Twopupsmom, one thing I have noticed while reading the forums here, how many grown children don't understand dementia or Alzheimer's... then they complain that their parent is doing this or that not realizing that is *normal* for the condition.

I really wish when doctor's diagnosis a patient with dementia/Alzheimer's that the Doctor insist that the grown child or the spouse spend some time learning everything about the disease to help them cope and to plan ahead. Set up seminars or classes for the whole family to attend and learn, learn, learn.

I know from this website here I have learned so much about memory issues, and have learned from my boss who's wife had Alzheimer's for 14 years. What an eye opener. This was all new to me. Even if my parents never get said disease, I feel so much better learning about it in case my sig other gets it, or if I get it.

One thing I have noticed are more featured articles in our local newspaper The Washington Post, which goes worldwide, regarding caregiving and with memory care issues. And more articles in the business section about reverse mortgages, about saving for retirement, and about the cost of caring for an elder at home, etc. That's a good start :)
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Oh it sure is a good start Frequent... The more the word gets out - why does it almost feel like how coming out of the closet felt for those stuck in there for years, Alzheimers "the Word" is Taboo to way too many, I like you follow other diseases etc that do not pertain to me or my husband, but I want to know, too much is hidden away from all of us, if you don't search it out, you'll never know. Just like food, finally the grocery store shelves & freezers are changing, getting rid of the ingredients in foods that have been affecting our lives for years. I'm getting off course here but all I have is time as a full time caregiver but I'm a great multitasker! I thought I would see on this site the fantastic findings out of Georgetown U just published 1 NOV of an off use of a leukemia med to help with the TAU in the brain of those with ALZ. Enjoyed reading your post
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twopupsmom, thanks for mentioning the Georgetown report... I just found it on-line and quickly scanned over it... wow.... not plaque but protein regarding Alzheimer's.

I remember recently seeing a report where two people with similar brain scans and the same amount of plaque showing, yet one had memory issues and the other didn't.... now that all makes sense that maybe it isn't the plaque. Clinical trials will start in a couple of weeks using the cancer drug nilotinib. Keeping fingers crossed :)
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Those studies are interesting, and the garner foundation...I was just thinking that is what we all need..at a glance, anyway! thanks for sharing! I will be reading up on these!
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Hi everyone. Its been a while since i've been here but its time. I've been seeing my caregiver counselor but our last meeting just didn't go well. the homecare coordinator wwas tellling her about problems with my mom and the caregivers. My mom is just so difficult with caregivers she doesn't feel she needs the help but I have to work fulltime and can't count on my brother to be there. We did hire a private caregiver and she seems to get along with her. STate paid agency they won't give me a schedule its different everyday, they don't do any light housekeeping from what i can tell they sit watch tv record things on my dvr, delete my shows and let my mom tear up the house. My brother just returned from his sixth vacation this year. Was complaining to me he didn't have as much money this trip....boo hoo i felt really bad for him. Constant pacing with her walker in middle of night (1am-4am) eventually she gets tired and goes b ack to bed. Tonight she had a horrible episode from sundowners or her brain injury i really don't know anymore.. She has had this brain injury since 16 and has always had mood swings but now all the hatred is directed to me and my brothers who do nothing at all get all credit and she just worries about them. I have been fighting with her old doctors so i finally got her a different doctor and will be taking her there on thursday and i pray to god they do something to calm her or help her sleep otherwise not sure what is going to happen. Tonight went through she wasn't eating and not taking her meds and i wasn't going to make her. Well I would have had to take her to hospital or eventually she would have seizures but she calmed down enough to eat and do that.
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todayall it seemed like i did was having crying fits...when do i run out of tears. but somedays its all i get is a few minutes away in the basement or garage and just have a good cry and then i can come back for more.
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chrissy I am so sorry for what you have to deal with is it time to consider placement-hopefully the new doc will be helpful-it sounds like it is too much for you-it sounds like the caregiver is not doing her job-can you get a different one?
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I have been advocating for a long time for people to do their own research and become informed consumers. So many people now spend hours reading labels in the grocery store but those same people might also spend a little more time exploring their diseases and drugs. They may not have medical training and understand technical terms but they would have questions to ask their healthcare providers and maybe get them thinking rather than mindlessly writing prescriptions.
Good for you twopupsmom. keep up the good work and continue to share. even if you only change the behaviour of one person it is worth it.
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Veronica91, I think professionals who write articles for the general public to read need to realize that not everyone will understand techno-talk and that is why some people don't even get past the first sentence.

Even on this website, once in awhile a contributing author will give professional advice and I am sitting there re-reading the article again and still scratching my head wondering what in the world is being said.... [sigh]
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FF I absolutely agree with you. it is essential to explain things in simple terms that anyone can understand and if a term is used ,for example to describe the symptom of a disease, then an explanation of exactly what is meant, should be added. Many times so called experts are merely self procliamed because they have a little experience and a lot of opinions rather than a PhD. I am talking in general terms here not just refering to contributing authors on A.C.
Consider the recent Ebola scare. We were told that you can only catch it by direct contact with an infected persons bodily fluids not by breathing the same air. Hubby and I were sitting here shouting rubbish at the TV (we do that a lot) If a patient sneezes in close proximity to an unprotected person you certainly can breath in the infected droplets that are released into the air. You can work that one out for yourself. Don't need an MD for that do you?.
However I stand by my comments that people do need to educate themselves and never agree to any treatment unless they fully understand the risks and benifits. If it is too much for the patient then they need to have someone with them who can either be authorized to make an informed decision or at least review the information with the patient and question everything. Drugs are very easy to look up and usually have a simple explanation for thy lay person. For example if you develop A fib and the Dr wants to put you on Warfarin or another blood thinner and you know you already have a bleeding disorder you need to know the risks and be able to discuss it with the MD
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Thank heavens for the Internet, as we now have the ability to do our own research. It gives me a tremendous sense of security being able to manage our parents' health,and my husband's, knowing I am better able to ask the right questions.
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Website for Georgetown U Article

techtimes/articles/19280/20141102/cancer-drug-nilotinib-may-help-cure-alzheimer-s-disease-its-all-in-tau.htm

Also Google
Molecular Neurodegeneration
All sorts of articles on ALZ I was able to get on their email list, it's for profs but it's very enlightening
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Veronica91, you are so right about having someone else with you when going to the doctor regarding an illness. I know when I was diagnosed with cancer I became a deer in headlights and didn't hear half of what the doctors were saying... thank goodness my sig other was there to take notes.

That's the reason I go into the exam room whenever I take my parents to the doctor. I find it somewhat comical whenever I am driving my parents home from an appointment and I hear them talking in the back seat.... it's like a Twilight Zone episode.... yikes, I thought I was in the same exam room with them with the doctor.... what room and what doctor were they seeing???
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Chrissy, siblings go on vacations but don't see that we, too, need a vacation. When I took vacation leave, it was to stay home and watch mom the whole time. I go back to work looking worse for wear. Finally my boss stepped in and said that when I take leave, I come back worse than when I left. He asked if I can pretend to go to work and find somewhere to stay when 'going to work'. Since then, I followed his advice. But, that's not like a true vacation like your brother and my siblings do - travel, hotel, restaurants, and not caregiving a bedridden parent. Then they have the nerve to say that they have no money to help out (as in hire an outside caregiver or pay for supplies, etc...)

Veronica, when the CDC and other doctors were saying that you can only get Ebola from body fluids and not from sitting next to someone in the plane. What?! The airplane is enclosed and the air is circulated. If that person sneezes or coughs and fluids shoots out, those things can stay in the air for about 30 minutes. I told family if it's only by body fluid, then why is it spreading so fast and easily?

Strange how the US (govt) is so determined to pretend that those shootings are Not Terrorist. That the Benghazi attack was by protesters and not terrorist. Then the Ebola situation -which we can only catch it through body fluids and not by sitting next to someone who coughs/sneezes. Yet, in Canada, 2 soldiers get run over and the shooting at Parliament, and Canada immediately declared it as a terrorist acts. Times are getting bad. This is not the time to pretend that everything is fine and dandy. It's not. Our hospital is not prepared for Ebola. The Naval hospital stepped up and offered their facility if it ever comes here. Our govt insists that they are prepared for Ebola. Hmmm...heard that same thing with the hospital in Texas. And that hospital is a more advanced facility than our small local hospital.

Freq, that happened to me, too. I was the patient. I brought my older sis and SIL with me at my appointments with the surgeon. They would say something that the doctor said - and I did not recall him saying it - at all.
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Oh, with regards to the engine light on, my car needed to be re-calibrated and there was a small leak somewhere in the engine. They noticed that my car was one of those that had a recall. So, they corrected it. When I picked up my car, they dirtied my driver's side window, and scratched my tint! I can't believe that they did that. I didn't have time to make a complaint because it was my lunch hour. I need to remember to bring wipes to try to wipe off that black dirty smears on the outside window.
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I have a specialization of 17yrs in ALS but when it's your parent some of that goes out the window. Working with the mentally ill I get some of the same responses as I do from my mom, but dealing with a client is much different. When they get angry or hurtful it's goes with the job, when your parent treats you like trash even though you know it's the disease not them it hurts all the same. I agree everyone should learn as much as possible. Example, my partner cares for my mom daily, I come in from work and take over setting up meds, emptying potty chair, checking chart of the day and home health notes, trying to get her to eat something more than cereal only to be told this morning it's our fault shes this way and that we never do anything for her. When we are up and down all night, exhausted and spent all our savings trying to give her the best last years of her life....it hurts regardless if its normal for the disease or not. This article ask "How are you doing today" and many use this as a tool to vent, give or get advice but at the end of the day caring for a parent with ALS is more draining than when my children were little not to mention when you realise your parent is now more of a child again than a parent that alone is disturbing. I'm very happy that more attention has been given to ALS because watching anyone slowly go into a confused dark place and knowing at some point the moments of clarity will be gone forever is the most depressing thing I have ever had to encounter :(
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Today I am tired. The last few hours of a 24 hour shift. Just horrable time with a new caregiver. She is gone now fo good. Bless this group.
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rfox, I've read that here over and over. It's so easy to maintain your boundaries, and patience when dealing with non-family members. That all goes out the window, when it comes to family members. I think it's because our emotions are involved. We're more vulnerable to their comments or inactions, etc... Like, "they should know better" or why it's harder to guard our heart from them.

This month is caregiver's month. I hope you all find a way to reward yourself, give a pat on the back. Somehow. I don't care to go to the movies - it's too loud - and I always come out with a throbbing headache. But, if you're into the movies and haven't gone to one in years, find a way to go. Or if you only have 1 hour, why don't you treat yourself to that restaurant you always wanted to go to? Or to your favorite restaurant? I'm kind of .... tight with my money. I think it's a waste of money to spend about $20.00 on a lunch at Tony Romas. I'd much rather use that money to buy more books. So, that's what I did to reward me - buy some ebooks. I can't wait to re-read it.
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boolluver - thank you for your advice. We have started making time for us and went away for a weekend. Of course got flack from family for doing that but I have shut most of them out of my life. We are trying to find a sitter for just one day so my partner can get away. I get to go to work but he feels trapped. Then we are going to cut back even more places to have the money for a weekend away at least every couple of months. As much fun as we had we spent one day sleeping with no one calling or ringing a bell. OMG it was so needed.
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Sinus acting up. Woke up this morning and felt something liquid dripping down my right nostril. Went to the bathroom and it's blood. My very first nosebleed. I remember in the old days, we were told to pinch the nose and look up. I also remember that they changed that advice ( like they did with someone having a seizure). So, as I got my kindle and turning on the Wi-fi, the blood was dripping faster and more. I don't like the sight of blood (thank goodness no more menstruation). So I'm telling myself not to panic (panic if the blood doesn't stop). One drop landed on my dress. First thing to pop out of my mouth.. "oh, gross!"

I finally got on the web and searched on how to stop a bleeding nose. I'm doing it now, holding a thumb pressing the guilty side of the nose. It may be a while. I've been popping excedrin the past few days for my daily headaches.

Two days ago, I tried making an appointment with the ENT, but found out that I need a referral. No referral, no appointment. I have an appointment with the new doctor at the other clinic this coming Wednesday.

It's past 5minutes and it's still bleeding. 718am and I have not changed dad's pampers. Will do more search.
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Wet the washcloth from the cold water tap. It stopped the blood flow but I definitely swallowed a thick fluid. Will carefully change dad's pampers without much heavy duty energy. Will stop by Kmart and buy a humidifier and more Kleenex boxes to keep everywhere..car, bedroom, etc..

I just learned why not to tilt your headquarters. Stomach would expel the blood out.yuck...by mouth...
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Poor Book, what a horrible thing to happen. Avoid blowing your nose, too, for a while - just wipe. You've probably popped a little blood vessel and they start up again in a trice if you're not careful. No infection, I hope? If it gets much worse don't hang about 'til Wednesday - isn't there a clinic you can get to before then?
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Book you did the right thing applying pressure to your nose. Sometimes you need to keep the pressure up for up to 15-30 minutes. If you can't stop it head to the ER but avoid that if you can. Can you switch to Tylenol instead of Excedrin? The same thing happened to me for two nights running. Mine was still easy to stop with the pressure even though I am taking Warfarin. I am not squimish about blood but a little goes a long way and makes a mess. How are you getting on with the Vicks in the shower for the sinuses. try disolving a teaspoon in a couple of pints of boiling water in a bowl. Put your head over and inhale with a towel over your head. Don't do this till at least a couple of days after the nosebleeds stop.
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My ent told me to put a little bit of vasiline in my nose (on the septum) when it gets too dry. Sometimes dryness causes nosebleeds. You know,, when you feel like you need to "pick it" LOL I have found this to work really well. Do not put the vasiline into your nose.. I grew up doing this.. it's BAD!!
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book, look for saline nasal spray at the drug store. It will help keeping your nasal passage moist. Make sure you are keeping hydrated too.
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Book, the excedrin may be the cause. It is a blood thinner, like low dose aspirin to help prevent clotting and resulting strokes.
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One of the saline nasal sprays is called "Ocean".
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