Sunday 11th February
.
A broken heart still beats
I know that to be true
Even though mine is crushed
And fractured into two
It continues with the rhythm
Beating for me and you
.
Love you sweetie
Precious Angel son
xxxxxx
Sunday 11th February
.
A broken heart still beats
I know that to be true
Even though mine is crushed
And fractured into two
It continues with the rhythm
Beating for me and you
.
Love you sweetie
Precious Angel son
xxxxxx
Beautiful!
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Thank you.
x
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You’re welcome.
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😊
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Yes a broken heart still beats and it takes a bloody long time for a broken heart to heal
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I wonder if a heart ever does heal after being broken.
That scar will always be there as a reminder.
x 💔 x
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Yes it will but you are able to give so much love even from loss
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Thank you so much for your kind and caring thoughts.
x 👼🏻 x
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I feel a bond with you as my uncle had multiple myleoma and because of the love you have for your son which inspires me every time I read you. I pray for your healing. I did read that MM can be treated with Stem Cell Therapy. I know you probably know a ton more than I ever could on this subject but I noticed they are now doing it in the US although not yet covered by insurance, and that it is very affordable if you go to MEX or India… anyway I know you probably know all of this and have researched it but I just thought I’d mention it on the off-chance. Prayers for you my lovely friend
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Thank you so much for your kind thoughts and prayers, they are appreciated.
Currently I am on year four of a five year clinical drugs trial, using targeted therapy in the adjuvant treatment of MM. It is a double blind trial, so I’m unsure as to whether I had the actual drugs, or a placebo, but whatever, I am so well looked after, having multiple appointments firstly every four weeks, then three monthly and now twice a year. Plus I see dermatologists, endoscopists, lymphoedema nurse and GP’s whenever the need arises. I have an appointment tomorrow, and two next week. It’s all go!
Hope you are well.
x
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Oh my friend I am SO glad you are going through the clinical trial. When diagnosed my uncle was told he would live 1/2 years, he lived in France where they had NO treatment that was any good especially the new stuff. He took Liatral and that helped him live 15 years from diagnosis (without other treatments) so I know in your case receiving treatment you can live also. I always wanted to bring him to the US but since he was sick before asking him to come over, it wasn:t an option. I am all for socialized healthcare but there HAVE to be other options such as clinical trials. I am so glad you are in one and I PRAY it is the medicine that you receive and that it will help you. I know people can outlive anyone’s expectations with the strength of God and their heart. I also know you continue on this earth to remember and love your son and I think anyone who was a child of yours was lucky indeed for that type of love. I pray for you my friend I pray hard, and often. Bless you and keep you safe. You are a beautiful soul.
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I am extremely fortunate that I have a wonderful team looking after me.
I feel very privileged.
Melanie x
💖
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Yet you survive and put so much love into this world and make it better.
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Ahhh, so kind of you to say.
Very much appreciate your words.
Thank you.
x
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I read all your posts and always pray not only for your son in Heaven but for you and your loved ones here on Earth. I know the distance is great but the love you have brings you closer.
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Such lovely words, thank you so very much.
x 💖 x
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You are welcome – I felt an instant connection with you when we ‘met’ here. My uncle had Multiple Myleoma and so I know some of your struggle and my heart goes out to you but moreover I am so touched by your love for your son I know he hears you and is SO lucky to have you as his parent because so many parents are not nearly as capable of the love that you are. I know from Heaven he watches over you and you will be together again, I know it with my entire being.
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You really are most kind with your words.
Thank you.
x 👼🏻 x
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Precious xoxo
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Thank you Lynn.
xx
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❤️
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💗
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