Topic : 05/30 Ask the Authors

Number of Replies: 235
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Created on : Friday, May 25, 2007, 01:13:05 pm
Author : DrPhilBoard1

Dr. Phil, along with authors Nancy Davis, Mitch Albom and Dr. Dan Siegel, share their secrets for living without regret and finding true happiness even when faced with a challenge. When you get married, it's '’til death do us part, in sickness and in health,’ but what if all of a sudden your spouse is diagnosed with an illness? When Nicole found out she had Multiple Sclerosis, she accepted her fate and learned to adapt. Her husband, Sal, has had a difficult time coming to terms with his younger wife's diagnosis. He says he wants to be supportive and help out, but is he really contributing to Nicole's declining health? Nancy Davis, who also has Multiple Sclerosis, shares her advice for helping this couple heal their marriage. Next, do you find yourself screaming, yelling and cussing with your teenager? Dana says her daughter, Whitney, changed overnight. Her grades went down, she started missing curfew, and she's been caught drinking and smoking. Dr. Dan Siegel shares the secrets for communicating with children and putting an end to the constant fighting. And, chances are you've read one of his nine best-selling books, seen one of his two critically-acclaimed films or tuned into his weekly radio program. Author Mitch Albom discusses his latest novel, For One More Day. Hear the story of a Dr. Phil viewer whose life changed after she read the book. Plus, Dr. Phil gives a previous guest a surprise that makes her already sunny smile shine even brighter! Talk about the show here.


Find out what happened on the show.

 

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May 31, 2007, 12:08 am PDT

Ask the Authors

Quote From: beckycaddell

I was diagnosed with MS in November 2005. I know what kind of a toll it takes on not only the person living with it, but also the entire family. I really sympethize with the guest and her husband and know what they are going thru. My husband and mom told me when i first started looking in to the possibility of it that I was borrowing trouble. After I was diagnosed, my mom was all about reading up on and researching this disease so she could try to understand what was happening to me and how she could best support me. My husband thought and still does, that there is a magic pill out there they just aren't giving me because I don't have insurance. If i try to tell him what is going on with me his response is usually 'Well I am tired too' or 'yeah well i am in pain every day but you don't hear me complaining'. A few months ago I came across a post called Understanding What Having MS Means. It was a big attention getter. I also sent it to friends and family. Most of the replies i received were 'thank you for sharing this with me', or 'I really didn't know MS could be that bad because you don't look sick.'

There are so many resources out there for people with MS and the spouse and kids who have to live with it. I have received help for utilities and rent from the local coalition and the MS Society. A Lot of the drugs needed for symptoms can be received free of charge or low cost thru the drug companies. My best advice is research all you can. Find out what is available from coping to medication. I also visit many online MS chat rooms and have made many new wonderful friends. It makes a person who rarely goes out in public seem much less secluded and alone.

I would be happy to post 'Understanding What Having MS Means' for anyone interested. The way it is worded helps people not living with MS understand a little more what it can do and just because you are 'sick' doesn't mean that you don't want your friends to come visit you or that you don't want to hang out or do things with them, it just means that sometimes you may have to cancel things last minute or when you are tired it means you are tired now, not wait 15 minutes see how you feel then. It is very powerful and encouraging.

Thanks,

Becky

Hello Becky,

I would like to read 'Understanding What Having MS Means'. my email address is gum_ba@hotmail.com.  I was diagnosd with MS in 2000 and I know how the guest on the show felt, in that my husband is still having a hard time dealing with it.  We've had some medical insurance problems and I haven't been able to take my Avonex in about a month and it's starting to worry him. He thinks that I will become worse. I tell him all the time to have a positve outook because I need that. When he's upset and worried, I'm upset and worried and that just exaserbates my symptoms. The less stressed I am right now with out taking the meds the better.  I am the kind of person that I'll worry about how you're feeling before I worry about myself and he doesn't understand that either. I could use some help around the house because I cant clean like was able to before, and I don't drive as often. I am back in school trying to obtain my masters' degree online, but I often feel guilty about that because here I spend money on medicine, but then I'm spending even more money on my education and I still have 2 sons to put through college. The guilt is enormous. but if  you would please post that or email it I would greatly appreciate it.

 

Thank You sincerely

Dawn from Oakland, CA

 
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May 31, 2007, 12:25 am PDT

"only a stay at home Mom"

Quote From: faithwalker

 I hate I missed watching your show today,  A  friend called to tell me about the show and how it was so informative on MS, and the stress that families endurer.
 
I to have MS, I found out March of 05, I have been taken shots every other day, they help me,  they hurt and I hate them with a passion, but I have to be strong for my daughters,  that is one of the things I do  to keep myself stong and healthy.
 My husband and I are getting a divorce, we have been seperated since April of 06, this has been the most stressful thing I have every experienced in my life..

My husband was and is having an affair, of course he is denieing it, but a fourteen page report of him in an hotel with her for two hours leads me to not believe him. We have been together for 21 yrs, married for 17 yrs.  After the divorce I will have no insurance, he wants the home sold, he wants money of course.

I hope you will have another show on MS,  and then another on controlling husbands,  I heard you had a great show on that a couple of weeks ago. ( My husband is one of those also)  I don't want to miss it .
I need to know a sure thing about how to get insurance on a pre-exsisting illness, for when the divorce is final,  I have been out of work for 13 years, and do not quilify for dissabilitiy,   I was only a stay home mom. 

I will admit I am worried about the insurance and cost of medications, and not knowing how bad MS will get for me. and then being alone. 

So I am a faithwalker who will do my very best to trust in a higher power.

I too am only a stay at home mom and a wife of a soldier.  Working outside the house just isn't the thing for me because I also have an incurable desease (UC), but i will tell you this there is not an "only" about it.  Being a stay at home Mom is the most important job one can have not to mention one of the hardes.  I feel for you with the insureance issue as much meds as I am on and the continung medical problems that creep up would be impossible to pay for without having military medical.  But always remember that in this day and age there are so many kids that do not have a parent tere as a 24hour parent and it is important.  Be proud of being a stay at home Mom.  Good luck I can imagine it will be a long hard road just don't let the stress get to the point that it makes your medical so much worse.  I have had to learn to control my stress and anxiety so that I do not have as many flair ups with my condition.  Once again good luck on your journey and congrats on being a Mom that is always there for your kids.

 

Karen

 

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May 31, 2007, 12:41 am PDT

I didn't sign up for this reply Life isn't Fair

Quote From: luvmyjenna

"I didn't sign up for it".

 

"I married a woman 9 years younger than me and I thought she'd take care of me when I got old."

 

"I'm afraid that that one day we'll wake up and she won't get out of bed.  That she's not going to be able to take care of the kids at all.  I don't know what's gonna happen."

 

Well, how the hell do you think Nicole feels?  Wonderful?  Is Nicole thrilled to think that she won't be able to care for herself, her children or her husband "in his old age."  I'm sure she's jumping up and down for joy at the thought of not taking care of selfish Sal, except that Nicole's just happy if she can get up out of a chair without falling over!  How do I know?  I was diagnosed with MS in May 2005. 

 

I'm sure when Nicole took her wedding vows "in sickness and in health" that she was looking forward to the day that she'd be able to wheel Sal around in his wheelchair, wipe his chin and change his Depends!  But then again, Nicole is lazy and playing up her MS by asking Sal to put the kids to bed when she has to go to sleep early because she can't physically stay awake.

 

After seeing this show, I am sooooo grateful for Rich, my husband of 21 years, that I want to run upstairs, shake him awake and kiss and hug him till he bursts. We don't have a lot of help or support from family and/or friends regularly.  After a long, stressful  day as a construction project manager, my husband comes home to our three children (12-year-old girl and 8-year-old twin boys, one who has special needs) and me, often a messy house, sometimes dinner unmade, me trying to catch a nap and the kids whining. Yet, he tries to pick up the slack.  He'll cook dinner, do dishes, fold laundry, help the kids with homework and whatever else that needs to be done.

 

It's not that he's a martyr -- he's not; he has a temper sometimes.  It's not that he's doesn't have complaints -- he certainly does.  Rich isn't always the easiest person to live with, but I know that neither am I.  Rich, for all his faults, has been my biggest supporter since my diagnosis.  He was the one who said we'll be okay and we'll get through it.  He has lived up to his word.  Every night at 9:00 p.m., Rich gets my Copaxone injection ready and administers it to me, because he knows I've been a needlephobic since we met (although less so now).  Rich takes the kids out on weekends to give me quiet time at home alone.  He drags the laundry baskets up and down two flights of stairs and does the laundry.  He drives the kids to their sporting events when I can't.  Despite the fact that I don't work anymore and we definitely are NOT wealthy, Rich doesn't object to hiring a housecleaner and a babysitter to help us when we can afford it.

 

I don't think Rich does all he does just because he loves the kids.  I think he does it because he loves me and is keeping his wedding vows of "in sickness and in health," just as I will do for him if that time ever comes.  He also realizes that when there's more stress on me, then my health will suffer, the kids will suffer and eventually his life suffers also.

 

By the end of the show, Sal, I actually believed that you do love your wife and worry about her, but you need to lay off the insults and step up the help.  You need to find a productive way to help your wife, which will come back to you in ways that you won't expect.

 

Sal, as I tell my kids, life is not fair.  It never is.  Especially to Nicole and your kids.  So, Sal, take some of your own advice:

 

"Get over it!  Toughen Up!  Give me a friggin' break!"

 

Life isn't fair, but I thank God everyday that he continues to sustain me.  I was diagnosed in 2000 I was 34 then and I thought it was a death sentence. My husband tries to be supportive, but sometimes his anger shows. He's afraid to go on vacation with me because I probably wouldn't be able to walk far, or I will get tired fast and I feel bad, but what can I do. I believe he should be doing anything for me, but he's very angry that I have this disease (that I didn't ask for).  We want to finish fixing up our home, but where is all this money going to come from. I want to go back to work (been off since 2005), I don't qualify for Social Security Disability, medicine and joining a gym to help me with my therapy costs lots of money. I sometimes feel like a burden on my husband, on my kids. My 3 year old is great, he's always asking me if I'm okay, if I feel okay, he holds my hand. My 13 year old is a little angry because he said it's not fair that his mommy is sick. I try to explain to him that life it's fair. That sometimes bad things happen to good people, but it's just the circle of life. I often worry about my sons because I read that usually a mother passes it down to her sons, so when my 3 year old starts to fall down outside i often think oh God did I pass it on to him.  The one thing I don't have is Life insurance, I'm not sure if we can afford it, I need someone to come and clean my house, If I could get some energy one day. I often watch people walk and remember when I could walk normal, or trott, or jog, or run even. I will run I will change I am Healed.

 

Dawn from Oakland, CA

 
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May 31, 2007, 1:32 am PDT

Nancy Davis

Listening to Nancy Davis has inspired me to take control of my life and health.  I have not been pro active with my health or my life.  I called my doctor right after watching the show to schedule the surgery that I have for long ignored.

 

I hope that you will have Nancy on again so that more people can learn to "get on with living" a great life!

 
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May 31, 2007, 4:30 am PDT

Hang in there

I was watching Dr.Phil and Nicole's story touched me. My husband is not very sympathic to me eiher, although he tries. I have fibromylgia, a degenerative disk in my back and I have to go june 29th to see if i now have arthritis in my knees and elbow. The past two weeks I have been in more pain than usual but I still have to work and do all the housework and whatever else needs to be done, while he lays on the couch and sleeps all day. I know he has problems of his own like diabetes, high blood pressure and high cholosterol, but he could help out more as could my mooching grown kids who live with me but don't lift a finger to help either even though they don't work either. When I get home from work i am exhausted and in a lot of pain and usually don't feel very well, but the only thing I get from them is that i am mad when i am not mad i am in pain.

Also I know about the yelling, My daughter is constantly in a yelling match with her 6 and 3 year old sons. I am a person that yells to a degree also.

 
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May 31, 2007, 4:30 am PDT

TY

Quote From: ceildh1

You are both lucky to have one another.

My inlaws (May they rest in peace ) were so much like that, as are my parents (though I am grateful my parents still have their health).

I remember my MIL getting ill and having surgery after surgery (we used to joke with her, "tell them to put in a zipper " she thought it was funny and laughter is the best medecine ), my FIL had to learn what he grew up with as Women's work (I remember how much of a mystery the washing machine was for him with a grin ), and how he would grumble about the " Damn vacuum cleaner being put in the back of the closet ".  When he got frustrated, we listened and pitched in.

He lost his license due to degenerative eye disease caused by diabetes, so it was up to us to drive them everywhere, that almost devestated him, he felt as though some of his independence had been taken from him.

He held her hand when she died, he pined away for another five years, officially, the Cause of Death, was Septic Shock, but I belive that it was a broken heart, he lost his will to live and nothing we did, or said made one bit of difference to him.  By the time he passed, he had both legs amputated, kidney disease, legally blind and severe heart disease, but it was an infected bedsore that finally did it.

I don't give up esily, its ironic though, just this afternoon, my husband was in a car acident, not serious, and he's home but sore ( that'll teach him to take on a dump truck, like I said I can be flip now, but on my way to the hospital, it was panic mode), and he's resting, I promised the doctor I would tie him down if I had to, but you know what, he'd do the same for me.

And you know, I'm sure you and your wife have some amusing moments helping one another, I hope you can laugh, and enjoy your lives after all we only get one trip through, and we can chose to live or be bitter about what we've been dealt.

 

And you.
 
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May 31, 2007, 4:33 am PDT

Living with disease

The show hit home in many ways. I suffer from several chronic painful diseases. I am so happy that Dr. Phil addressed Ms and how it affects ones life. I hope that in the future he continues to do so. My live in hasn't abandoned me but he doesn't say much about it either. He does not treat me badly, in fact when needed he pushes the wheeelchair! His way of coping with it is to make light hearted fun of it. Some people might not like it but he isn't making fun of me he is joking about the weird affects the diseases has on me sometimes. That is his way of coping. the humor makes me laugh and makes things easier. I gave him the option of leaving when we found out what was wrong with me but he said its no big deal just remember that when I am old you will be taking care of me!
 
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May 31, 2007, 4:34 am PDT

Good Message; Wrong Person

Quote From: amcburns

You seem to be a person of great inner strength and that is to be applauded.  However, MS, along with other diseases, affect each person differently.  It is not fair that you would say it is the "easiest" to deal with.  I am sure that there are people who are worse off then I am, but I also know that I am worse off then some others I know with the disease.  My concern is that you seem angry that her experience is not the same as yours! 
I think you meant to reply to the same person I replied to.
 
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May 31, 2007, 4:52 am PDT

A Different Look !

Reading some of the Message Boards I get the picture that when women are faced with contracting MS or other bad diseases, it's distressing to me to think how much we dread sharing ourselves with our diseases to  our partners. As if the sick partner really wanted to get sick!  It's sad that the women who are sick are filled with guilt and feel as if they are burdening the male partner. It just doesn't seem fair to me. If the partner is committed, shouldn't he or she love the sick partner more?
 
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May 31, 2007, 4:52 am PDT

Mitch Albom

I'm currently reading Tuesdays with Morrie and find it absolutely riveting. After the show, I find myself debating buying One More Day. I know what the problem is - my family doesn't communicate well, and we were brought up not to show tears. Do you think maybe a letter is the answer?                 jaycee554
 

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