travel with thalassemia mayor

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Offline Supergirl

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Re: travel with thalassemia mayor
« Reply #30 on: July 03, 2011, 04:45:32 PM »
All the best...I guess it goes out to prove that 'we can achieve whatever we set our mind to'....thanks thalpal for being there to help in this journey and many more.
SK

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Offline Dori

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Re: travel with thalassemia mayor
« Reply #31 on: July 03, 2011, 08:44:45 PM »
I hope you can read this very soon. I would suggest you to tank up in Hamburg in UKE hospital. I do not know Danmark. You can also send me an email.

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Offline Andy Battaglia

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Re: travel with thalassemia mayor
« Reply #32 on: July 03, 2011, 10:09:27 PM »
If you need any advice concerning Denmark, contact our member Ironman (Kocher).
Andy

All we are saying is give thals a chance.

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Offline Dori

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Re: travel with thalassemia mayor
« Reply #33 on: July 08, 2011, 09:09:20 PM »
He had his blood transfusion today in my unit. All went well, isn't it?  Afterwards I showed downtown Amsterdam. Tomorrow he leaves for Paris (France). His experience to get a shot of viking blood is very sad and funny. He has not easily access to internet nowadays.

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Offline troll205

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Re: travel with thalassemia mayor
« Reply #34 on: August 26, 2011, 05:47:12 PM »
I'm still without internet :(

now I'm in the Spanish Pyrenees, Catalunya. :biggrin

until now 7 transfusions abroad:

Sabadell - Spain...THANKYOU LAURA!!!! :ty

Villaiojosa-Spain

San Sebastian-Spain

Stavanger - Norway...Norwegian doctors are convinced that if you sleep (only sleep in the night...no in the day!!) 1 night in a bed in a European hospital you have a bacteria that  not exist in Norway  ....crazy! :rotfl

Amsterdam - Neederlands... Dore.... thanks again and again!! :thankyou

2 in Girona - Spain

I tried to do a blood transfusion in Millau (France), but they asked me to payed 600€ for 2 bags of blood but with my italian insurance only 200 € in cash after the transfusion!!!! :mad

@$#%  YOU FRANCE!!! :mad

the journey continues! :biggrin

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Offline Laura

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Re: travel with thalassemia mayor
« Reply #35 on: August 28, 2011, 08:48:26 AM »
Hello!

I'm so glad you could come to Spain again and solve your "French problem".

Where are you travelling to right now?

Hope everything will be easier in other countries.

Kisses,

Laura.
The most important thing in life is not what you achieve but the fact of fighting for it.

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Offline Laura

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Re: travel with thalassemia mayor
« Reply #36 on: January 28, 2012, 12:22:44 AM »
Hello!

Are you still traveling? How is it going?
The most important thing in life is not what you achieve but the fact of fighting for it.

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Offline jotembe

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    • Thalassämiehilfe ohne Grenzen e. V.
Re: travel with thalassemia mayor
« Reply #37 on: February 24, 2012, 05:36:23 PM »

Hello Laura,

he hopefully didn't get lost? Did he?
Tough guy this one.
Even in my younger days I would have assessed it as too exhaustinng.
I hope  that he soon might able to answer.

Greetings from Germany

Juergen

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Offline Laura

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Re: travel with thalassemia mayor
« Reply #38 on: February 24, 2012, 09:37:01 PM »
Hi Juergen!

I'm sure he didn't get lost. He might be somewhere around Europe...

Best Regards from Barcelona!

Laura.
The most important thing in life is not what you achieve but the fact of fighting for it.

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Offline jotembe

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    • Thalassämiehilfe ohne Grenzen e. V.
Re: travel with thalassemia mayor
« Reply #39 on: February 25, 2012, 08:36:33 AM »
Hello again Laura,

Five month without any sign of life / post? That seems very unlikely to me.

Best regards to Barcelona - one of the most beautiful cities of Europe

Juergen

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Offline Laura

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Re: travel with thalassemia mayor
« Reply #40 on: February 27, 2012, 10:38:43 AM »
Hello!

I think he's not really used to write in the forum, that's all. However, I'll send him a text and I'll tell you the feedback.

Kisses,

Laura.
The most important thing in life is not what you achieve but the fact of fighting for it.

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Offline jotembe

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    • Thalassämiehilfe ohne Grenzen e. V.
Re: travel with thalassemia mayor
« Reply #41 on: February 27, 2012, 12:11:45 PM »
Very kind of you, Laura!

Thanks a lot!

Warm regards

Juergen

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Offline troll205

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Re: travel with thalassemia mayor
« Reply #42 on: March 05, 2012, 07:34:18 PM »
Hello everybody!
Thank's Laura for the text. My travel finished in november but I'm still living in my autocaravan in Trentino-north Italy. It's 1 year that I live in my autocaravan but the 15 of March I will rent a house because my girlfriend gets a job here. I know that there's an other thalassemic italian guy, Luca, who wants make a journey for some months. I hope he will write his travel here ;) If I have some news I will write here.

Thank's for all!!  :hugfriend

My girlfriend Giulia sends you a greeting!!

See you!

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Offline Laura

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Re: travel with thalassemia mayor
« Reply #43 on: March 08, 2012, 07:58:44 PM »
Hello and welcome back to the forum!!!

I'm glad your girlfriend got a job. Hope you'll find one also.

Did everything go well then? You have to tell us about the different places you've been. Maybe you could write a list of cities and hospitals you've been.

Big kisses for you and Giulia!

Laura.
The most important thing in life is not what you achieve but the fact of fighting for it.

Re: travel with thalassemia mayor
« Reply #44 on: October 15, 2016, 03:57:21 PM »
Hi everybody
I'm a master graduated of University of Tehran (the first-ranked university in Iran). I'm going to immigrate abroad for several years, but I could not do because of my disease (major thalasssemia). I have researched about costs of treatment include of blood transfusion, drugs such as Exjade, doctor visiting and yearly checkups and heard up that they are too expensive and i can not pay them myself. I'll highly appreciate your kind to help me about some questions:
- These costs in which country in Europe or Canada, Australia is cheaper?
- How can I receive freely services I mean how can I become under support of an insurance organization? for example student Visa, Work Visa, emigration?
- If I attempt to apply and take admission from a university, I will have complete insurance for my disease?
- and the last question: Is there anyone who can give me a contact number or information about an organization which know about my disease insurance to help me?
Thanks a lot

BR,
Setare Sadeghi

 

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