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,

I know what you mean. When my grandaughter was in so much pain, I

would have given any thing had I been able to take her place. But

we all have our own role in life that we must play. I had a friend

discribe it thus: We are all standing in our own places along the

wall of a fort and we can't leave our appointed spot, but even

though we can't rush in and take over for someone else, we can call

out encouragement to each other. That makes all the difference. It

really does help when you share with the rest of us. It helps to

know I am not the only one who feels that way. I am so glad I am not

alone in this anymore.

Joanne

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thank you Laurie,

" Unto everything there is a season " even for crying.

Smiles,

Re: guilt

>

>

> Please know that I am thinking of you, your daughter and husband. Please

> vent as you need to. It also helps others as well as yourself. It may even

> allow us to cry and help deal with our frustrations.

>

> Thinking of you,

> laurie

>

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Oh Alice,

thank you so much for your kind words and for letting me let it all out

when if flows over. Thanks for being such a good friend..... My admiration

for you is equal!!!

Morning has broke and with it comes hope and thankfulness for a new day.

Smiles to you,

Re: guilt

>

> ,

>

> We have been good friends since the day we found one another on the

internet and you have always been a huge support and very positive despite

the pain and suffering you live with each and every day. You have given so

much of yourself to people in at home but even more so those in distant

lands who probably have your face etched in their hearts forever. Your

faith is amazing and I am one of those people you have touched along the

way.

>

> I'm glad you took the time to share your grief tonight. Part of dealing

with it is letting it out. You are not made of stone. You are made of flesh

and blood with a warm and loving heart. Of course it hurts to see your

child dealing with what you feel you have passed on thru your genes.

There's no way to avoid that if you have any love at all. What we have to

do is not blame ourselves and I know blame and guilt are somewhat the same

but I really think that what we feel inside is more distress and perhaps

some anger that we have passed it on without knowing. We would take it away

in a second if there were just some way to do that. This is why I am so

active as an advocate when my physical body says to stop. I seem to do less

and less but I refuse to give up until they lower me into my grave. Just as

you are seeing, I am seeing my daughter's deal with the disease earlier than

I realized that something was wrong and of course, even more in my

grandchildren.

>

> My opinion of this is that it's natural to grieve. We just can't let it

consume us. We need to take that grief and make something postive or it.

If anyone on this list can do that, I know it is you.

>

> I'm sorry you couldn't accompany your husband to Honduras. Knowing you as

I do, this must have been very difficult. It might be a good time to spend

some special moments with that mom to be. I know she would probably love

that.

>

> Please feel free to vent on this list or privately. My listening ears may

be deaf but they are virtually alive and well.

>

> Hugs!

> Alice

>

>

>

> Medical advice, information, opinions, data and statements contained

herein are not necessarily those of the list moderators. The author of this

e mail is entirely responsible for its content. List members are reminded of

their responsibility to evaluate the content of the postings and consult

with their physicians regarding changes in their own treatment.

>

> Personal attacks are not permitted on the list and anyone who sends one is

automatically moderated or removed depending on the severity of the attack.

>

>

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,

We are honored that you felt this was a safe place to share your

feelings about your daughter's situation. Genetic disorders carry

their own peculiar kind of grief. My mother has said many times that

she wishes she could take all my symptoms, and I would do the same

for my son if I could. They cut the umbilical cord at birth, but

they can't cut the emotional and genetic ties that bind us to our

children and grandchildren.

I will keep your family in my prayers.

Barbara

> I know the place guilt plays in our life for those who have passed

this disease onto our children had been discussed several times.

And while the reasoning power tells us it is not our fault, and

indeed it isn't, there is still a connection that no matter what is

said, cannot be errased.

> Tonight, before ever hearing about Mattie, I was near tears as I

heard my daughter who is now pregnant tell me of her pain in her

muscle that just wont go away the last few days . She has had

muscle pain since she has been 3. This is not new, but it has

progressed, And here she is pregnant and can't even take anything

stronger than a tylenol for it. My heart is wrenching as I know the

pain/fatigue she is feeling and that she is much worse than I was at

her age. I try to share it with my husband and he goes all to

pieces over it as he has watched me suffer so and my life be changed

so drasticly. He is a great suport to me. the best! I couldn't askl

for a better understanding husband. But when it comes to our

daughter he can't handle it at all and falls all apart, so I must

bide my tongue and keep it all in. The point I am trying to make is

that my heart is going out to Jeni so much, she has lost all her

children to this and has to wonder what her future holds too.

Although at this point I doubt she cares. Mattie certainly has

touched a lot of lives and his life was that of triumph, no matter

how short it was. he was a blessing indeed. We each need to be

that.

> Not that I am anywhere near the situation he is in. I am as

healthy as a horse compared to him or some of you. But the

pain/fatigue can be great.

> My daughter has not been diagnosed, all though we are certain that

she at least has the McArdle's. She is now at the point tonight she

thinks she does want to have the biopsy. I think I will pay for her

to fly up and have it done in Boston by my doctor where she won't

be blown off as 'its all in your head " he has been aware of her

situation for years.

> I think of the times when my kids were little and I was so

fatigued I would lay on the floor next to them while they played as

I had not enough energy to get up, and didn't know why. I like the

rest of you, think, I would rather have my share of her pain and

fatigue if only she didn't have to have it. hearing about Mattie

tonight and then my daughters email and phone call has got me blue I

guess. I am usually not like this. but it is normal for us all to gt

down at times. I just don't stay down. it usally only last a matter

of hours. I am thankful I have all of you to vent to. My life has

been one of service and I intend it to be that way until the end.

Even if all I can do is pass a smile on to others. But for now, I

still touch many lives and while it is no where the amount I want

to, I am so thankful for those that I can make a difference for.

Okay, I got all my boo hoos out, I can cheer up again:) Sorry this

is so long. ( I am also " under the influence " at the moment, ) not

alcohol but prescription drugs. home alone as my husband had to go

back to Honduras without me today and am feeling bad I had to miss

out on that. But...........

> Thanks for listening,

>

> Smiles,

>

>

>

>

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thank you Barbara, It is wonderful to have a place to feel safe at.

Smiles,

Re: guilt

> ,

>

> We are honored that you felt this was a safe place to share your

> feelings about your daughter's situation. Genetic disorders carry

> their own peculiar kind of grief. My mother has said many times that

> she wishes she could take all my symptoms, and I would do the same

> for my son if I could. They cut the umbilical cord at birth, but

> they can't cut the emotional and genetic ties that bind us to our

> children and grandchildren.

>

> I will keep your family in my prayers.

> Barbara

>

>

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