Diana Chamia is a young blogger from the School of Journalism in Mahajanga, Madagascar and has proved more than being a very skilled writer, she's a true social activist. Connect to her blog and Foko Blog Club  to know more about this family she's helping. Your attention and donations are welcome here and Foko will transfer the totality to the persons in charge.

[http://dianachamia.wordpress.com : Help me helping them April 19th. 2008]

August 2007, Philomène Georgine gave birth to wonderful twins : a little girl who was perfectly healthy and a little boy. He was born with a very difficult condition (please take a look at his picture) a flesh lump on his forehead between his eyes and on the top of his little nose. It masks his eyeshight and gives him respiratory problems. " During a month and a half, my kids and I had to stay at the hospital because of this disease. But during this time, nobody cared for us and you are the first who really shows interest in my children's well-being. And the first one to smile at them. You know, everybody hate us." I am a washerwoman and I don't have clients anymore because people rejected us. My husband left us when I was still pregnant. And doctors didn't diagnose my son and nobody helped us finding a solution to cure him. " said the mother Everywhere in the country there are hundreds of children malformation but Majunga is a little town and most people must have heard about our story. Why do people hate us? She hasn't asked for what is happening to them. There are beggars, people with no food, … but they are not in this situation. What can a woman with no money, work and husband with 1 sick kid to care about can do? And nobody care for them. How did I met this kid? I took the Bus no 5 from home to Bazar Mahabibo but I was too dreamy or maybe it's this kid's destiny, I missed my stop. We were already at the City hall stop when I realized my mistake. On the way back to the market, I saw this lady who was bearing a kid on her back, one in her arms and a big red bag on her shoulder. The one in her front was shielded with a green sari. (I was wondering why did she has to use such protection under the very warm Majunga weather). A wind blow discovered the child's face. I couldn't believe what I saw before my eyes and couldn't keep myself for expressing my surprise with a "My Godness". Of course the mother turned back to protect her child and started to walk very fast. But you can't escape this easily from Diana chamia. I followed her and told her to rest a little away from the heavy sun. She stared at her child and accepted to rest under the City Hall centenial Flamboyant tree. It was there when she told me about her story and asked me for help. I took my promise and went to the Leo Club of Majunga president. He told me to get to his fundraising on April 26th at Lycée Philibert Tsiranana to show the picture and bring Georgine's story to these well-intended people.

Thanks to everyone's enthousiasm and Malagasy blogosphere intense activity, Foko is able to start the next move to support Diana in her personal initiative to help this poor family. More than a dizain of Malagasy bloggers have teamed up to start a fundraising project and are patiently waiting for Diana's news. We are also looking for a local organization which can give her their full support in Mahajanga. If you're involved in a heatlh related NGO working in Boeny Region, please contact us at Foko [info@foko-madagascar.org]. 

[Update: Help me help them - part 2 - May 2nd]

On thursday I went to the studio for the picture I posted on my blog then I went to Lycée Philibert Tsiranana for my meeting with Leo  Club (the Youth group of Lion's Club). When I arrived the president introduced me as a Leo from Diego-Suarez (Madagascar's northern town where I am from). I told him that I wanted to be talk before the Leo Club here in Majunga because I wanted to help little Kamba.
But when I started my speech, the president looked weird. "Sorry Chamia no Lions came, you know, they are not interested in your case. It's too much for them, well…Lions are only taking care of visual  diseases like cataract and blindness, we are not specialized in this one.
I insisted on saying there must be some impacts on the optic nerve and the flesh is obviously blinding this baby's eyesight. But apparently my ideas weren't catching his interest and he pursued on saying "I 'm sorry Chamia I know what you want…"
I couldn't wait for this charity to finish so I lef before the end. My left ankled wasn't healed ye (Diana took motobike lessons earlier this week and had a little accident which made her go to massage sessions) so I felt a little pain and a lot of sadness. I'm still very sad. I don't know what to do, Lions Club was my only hope, they let me down. What can I do now?
But I won't fail my promise to Kamba's mother and do everything that I can to help her son.

After this overwhelming post and the message she sent to Rondro (Ikalamako) and Joan (Jogany), the two of us planned an open chatroom to exchange ideas, networking and experience on  what could be the best move for Diana. On May 3rd, the bloggers committee agreed on : 

  • Letting Diana taking full control of her initiative and have the last word on any decision (of course she will contact the family before anything will be decided). 
  • Waiting for Hanitra (Sipagasy) meeting with Stéphane (Foko) in Madagascar where they'll have more about the situation and start to contact health organizations and doctors.
  • By May 19th, we will gather all the informations to start the fundraising movement in order to support this family financially and send them enough money for their very first diagnostic.
  • The committee and Diana are always open to your suggestions and questionning. Since this is Diana first try at global fundraising and with class schedule (which didn't keep her for being the most activist among us all), we're asking for everyone's comprehension and discretion.

 [Update: Message from Bako and Jean - May 10th] 

Merci du chaleureux message à notre endroit et il nous ferait grand plaisir de vous voir parmi les personnes qui vont nous encourager le long du parcours de 21 kms le 25 mai prochain. Merci aussi de nous faire savoir l'existence de Foko Blog Club. Le cas de l'enfant né avec une malformation congénitale à majunga me touche personnellement sur plusieurs plan étant moi-même un ancien de Majunga d'où mon père est originaire et où une bonne partie de ma famille vit encore. L'école de journalisme de Majunga me concerne un peu sussi sur le plan personnel étant un ancien journaliste de Majunga conscient des difficultés de la presse régionale .

Thank you for your warmful message and it will please us to see you cheering us up next Saturday May 25th for the 21 kms run to raise fun for little Kamba in Ottawa. Thank you also for telling us about the Foko Blog Club Project. I felt personnaly appealed by the baby's malformation and also because I am a former journalist based in Majunga. Most of my family still live there and I feel also concerned for the School of Journalism hard time to get the visibility its deserves like all regional media in Madagascar.

 [Update: Who are Jean and Bako - May 15th]

Minutes after I had a very fun phone call with this nice couple from Ottawa with very strong roots in Majunga, they sent us their pictures from the villages they've been helping. Jean also told me that all he was doing wasn't in the intention to look genereous or philanthropist, it was only because the mother and children situation touched their heart. I would add : they are great inspiration for us all. We will be hearing in the upcoming days from Max (Jean cousin's in Majunga who is taking care of the family) who will make their first 120$CAN donation in good use by taking them to a neuro-surgeon. What will happen next is not only up to the people who already helped but us who are willing to do something … Take in mind that Philomène is only 20 with 3 kids we will have to also to take care of them and finally project into their finally future. 

Bonjour Joan,
On aurait voulu faire plus mais on n'a pu faire que ce qui était à la portée de nos moyens bien modestes. Pour le cas de l'enfant à Majunga, je n'ai fait que parler au téléphone et écrire des messages. C'est Diana et Max qui ont fait tout le travail, n'est-ce pas? En tout cas, merci des mots gentils à notre endroit et on se demande si on le mérite. Nous sommes convaincus qu'à plusieurs on viendrait à bout d'aider efficacement cet enfant qui a tellement besoin de notre coup de main. Entre temps, si le coeur vous dit de voir les photos des gens des deux villages que nous aidons à Madagascar, voici les liens. Quant on regarde comment les yeux des enfants dans ces photos brillent de joie et d'innocence alors que nous n'avons apporté que très peu, cela nous poussent à faire un peu plus. Car le jour où ces yeux ne brilleront plus de joie et d'innocence, le pays aura franchi un point de non retour. De la vitalité de nos campagnes dépend l'avenir de Madagascar car la nourriture qui arrivent sur les tables en ville, d'ou viennent-elles? Il faudrait dire aux jeunes dans les villes de respecter les paysans car sans les paysans, nos campagnes qui sont nos sources de vie disparaitront et nous avec. Bref, voici les liens:
[Update: Max came to the rescue !  ]
We were very happy to hear from Hanitra our envoyee in Madagascar (well she happens to be there on vacations and wanted to help out as well). She already knows Stephane from her frequent blogging with Foko and will be introduced to the other bloggers she will award with gifts and prizes. Diana in Majunga received a phone call fron them both this Thursday afternoon while they  met at Teknet Antananarivo.
Again Max name was mentioned and we already know about him from Jean and Bako. They are relatives of Max who is currently living in Majunga and contacted Diana shortly after the news abotu this baby came out. He will be our contact with the family since he is kindly involved in every step of this great project. On sunday a surgeon will check on the kid and will give Max and Diana the results if either they will move to Antananarivo or not. Whatever happen on Sunday, we will be ready to help them right?
Stay tuned for more news from baby Kamba.
and again Thank you Max
Podcast : http://www.foko-madagascar.org/podcasts/dianahanitra.mp3
[Update: First diagnostic out !May 18th ] 
Bonjour Joan,
Je viens de parler à Max. Il est allé voir l'enfant avec le neuro-chirurgien. Diana a été prévenue de la visite chez la famille mais n'a pas pu y aller. Résultat de la première consultation : le neuro-chirurgien est optimiste et voudrait voir l'enfant hospitalisé à Tana le plus tôt possible. Il parlera avec l'hopital dès la semaine prochaine pour voir combien cela couterait pour l'hospitalisation. Mais comme il y a l'autre enfant car parle de jumeaux (un enfant avec malformation et un autre enfant en bonne santé), la mère ne peut laisser cet enfant seul à Majunga. Cela fait que sa soeur va faire partie du voyage pour aider la mère à prendre soin des deux bébés. Le neuro-chirurgien a dit que l'hopital a des chambres privées où les 4 peuvent rester durant l'hospitalisation de l'enfant ayant des problèmes. Je suis en posséssion de 200 dollars canadiens actuellement résultat de notre levée de fonds.
I just spoke to Max. he went to the family with the neuro-surgeon. Diana couldnt make it but is informed about the situation. The resuts are very positive : The neruo-surgeon is optimistic and want to the child to be hospitalized in Tana as soon as possible. He willtalk to the hospital staff next week to know about the fees. but he know there is another kid involved (Kamba has a twin sister who was born heatlhy). The mother can t leave this child in Majunga so we have to bring her sister to take care of the other baby too. The neuro-surgeon told us the hospital has private rooms where the 4 of them can stay during the child hospitalization. I was able to raise 200$CAN (reminder: Jean and Bako the Black Angers have already sent 120$ to the fanily earlier last week!) 
 Le voyage sur Tana se fera probablement le 2 ou 3 juin. Alors, c'est le moment ou jamais de manifester notre soutien à cette cause. L'enfant sera opéré à Tana le plus tôt possible après confirmation par scanner qu'il n'y a aucun organe vital dans la "bosse". Sinon, ce sera un peu plus difficile mais pas impossible. Mais on ne peut rien dire à ce stade-ci. Seul le scanner permettra de déterminer avec précision la situation réélle.
Voila, je pense avoir tout dit. Je vous tiens au courant dès que j'ai d'autres nouvelles.
The trip to Tana is scheduled on June 2nd or 3rd and it is about time we manifest out support to this cause. The child will receive healthcare as soon as possible and the scanner will confirm if there are vital organs touched by this malformation. It could increase the difficulties during the operation but it is not impossible. We can say anything at this point. I will keep you guyz updated as soon as I get the latest news.
Regards, Jean Razafindambo
 
[Update: We're waiting for your donations at Zaza-Vavy : http://www.zaza-vavy.org]

 

Many already know around the blogosphere and internet about this sad story of one year-old baby Kamba Antefindrazana born with a malformation. It was Diana Chamia who first published about the family when she started at FOKO_Majunga and wrote : “Help me Help them” as she promised the mother to do whatever she can  in finding solutions for the baby. Since then many of her friends relay her hard work and discussed about the ways to support her efforts, all actions related to this story has been carefully summarized here on Malagasy Miray:
http://malagasymiray.net/2008/05/02/help-diana-help-them-bloggers-committe-on-the-way/
Today we can start our global call for solidarity after the first surgeon in Majunga accepted to take care of the family and planned to move them to Antananarivo for a better diagnostic. This trip needs your financial support and the committe is aiming to raise 500$ for the first fundraising. There will be also medical costs and daily expenses for tg family since Kamba has a healthy twin sister and another big sister her mother Goergine has to take care of.
Of course we will update you gradually on the process and will share all  the informations and news we have on this great initiative.We can’t thank you enough for your help and support to this family and baby Kamba. Everyone involved has already spent amountless time on networking and brainstorming  we also want to thank them for caring this much. If you happen to  be in Madagascar and available to help out by the time please contact us .

From Diana Chamia, Kamba’s family and the committee

 UPDATES ARE NOW FREQUENTLY POSTED ON ZAZA-VAVY BLOG
 
 


 
 
 

 
[Update : June 1st : Preparations for Antananarivo]
Max, Stéphane and Diana met finally in Majunga and join Kamba's family to organize the Antananarivo trip. The committee didn't rest on the other side of the globe and Jean and Bako, Joan and Rondro managed to send the funds and contact everyone in Antananarivo to be ready for  their arrival. Diana will bring the family by taxi-brousse to the capitale this Monday evening and our contacts in town are in place to receive them before they meet the surgeon. This person (a friend of Jean Razafindambo) has already all the papers in hand to make the diagnostics and reveal the baby's situation. Once he knows exactly what is going to take to operate the baby, the amount of money left to raise will be unrevealed. So be ready people !!!
 
 

 

[Update : June 3rd : Message from Diana]

salut devine ki è avc moi? Hello guess who s with me? We arrived in Tana and Mavo (ikalamako sister serves as chaperont to Diana and guide her through the city) si currently writing you a mail. I have to leave now we re lost in the labyrinth of HJRA (Hopital Ravoangy Andrianavalona , General Hospital in Antananarivo) with Kamba s exams for tomorrow. Take care

bjr,onè deja a tana et maintenant moi Mavo ta soeur (ikalamako sister serves as chaperon to Diana and guide her through the city) on est entrain de t'ecrir,voila je te la laisse salut Ne on traine dans le labyrinthe HJRA avec le bilan de Kamba a effectuer demain,ben on te laisse pour l'instant et a+

 [Update : June 7th : HAPPY BIRTHDAY KAMBA]
Please read Diana's blog for the latest news and more pictures are coming!! 
 
 [Update : June 7th : KAMBA  undergoes first chirurgy]
We heard on sunday that Pr Clément was ready to operate baby Kamba. at 11 am on Tuesday . Thank you for your kind thoughts and more informations will be made available very soon.
 

http://dianachamia.wordpress.com/2008/06/16/kamba-et-ses-etoiles/

Room 129, it's the room for macrocephaly babies , I went there maybe because of curiosity but especially because there were children. Once I got there I saw this dwarf lady with her macrocephaly baby.

I went to them and we talked for a while and she told me she was poor and had no money but I knew she was lying because they weren't treated as regular patients and having little privildges (for the meal for example). I told her I was penniless too but remembered Mavo game me 2000 Ar and gave it to the lady (I hope Mavo doesn't read about this because she gave me the money for internet connection)

On Monday 9th at 9 am, the little lady came into our room very joyful and looking a lot like Snow White afte she was awaken. She told me :
– Come with me I want to help you..
– You helping me? what is happening I don't understand, I asked
– Come with me because you need something for the baby you grought with you for his surgery. It's a medical valve for after the operation and it costs a fortune. And if you come with me you can get it for free

The nurse agreed with her and urge me to go with the lady. We went together to a house near a Jovenna gas station. We went upstairs to the first floor and an old monsieur who looks a lot like a morroccan was in his office. She said :
-It's her

At first I felt scared because we were at a very dark house with not suffisent lighting around and I had no idea where we were. By the time he started to speak many images developped in my head ; I thought they were organs traffickers…
– Is it you who came here with the child with a big nose ?
– It is not his nose, it is called a frontal Meningocele
– You know the name, I thought you weren't aware of it
– I know a lot because the ex-minister of health explained it to me and then I checked on the internet and it is due to a folic acid deficiency at the first month of pregnancy.
– Great you seem to taking good care of him , the thing I want to give you costs 5 000 000 fmg and you deserve to get it because she told me about your dream to hlp this baby.

I was speechless and the only thing I managed to ask was :
-How much is it again?
-1.000.000ariary=5.000.000fmg, and if I have enough time I will visit you at the room 125 for neuro-surgery patients, and if there is anything else I can do for you don't hesitate to come by, ok Diana?

I nodded and found nothing else to say but when I had my mind cleared I was already thanking him so many times I think he was starting to get annoyed. Then I thanked the lovely lady who now looks more like fairy to me. How can I imagine that a woman I visited earlier this week at room 129 could help us this much when I only gave her 2000 Ar at first place.

When I came back at the hospital, put the medical valve in the box for Kamba's things ready for the operation and told everyone about the miracle.

Tuesday 10th, everyone has only one thing in their mind "it's today Lord help our little one". At 11 am, they took him at the bloc and all the stars shined only for Kamba. Only one person could attend the surgery with him, since Georgine wasn't really ready, Mavo decided to assist the baby in her place. It was done at 3 pm, and cried, I was thinking to myself "well he is crying it means he is alive". The first step of the process is now accomplished , we're waiting for the second surgery. Poor little kiddo was crying because he was hungry, we couldn't give him food from 4 am. 3.23 pm his mom is allowed to feed him, he can sleep thight now.

 

  [Update : June 27h : KAMBA is doing fine]

Bonjour (bonsoir) tout le monde,

From Rondro Volantsoa ,a Malagasy blogger from Rome, Italy the most active "zaza-vavy" whose sister Mavo  is Diana's chaperon in Antananarivo and doing most of the "supporting" at the hospital (this includes answering to Joan's frenetic phone calls, taking care at meals, sewing the baby's operational suits…)
"Thank God, Kamba is looking pretty again!" was the first sentence from Mavo when  Rondro called her 30 minutes ago.
She kept on saying : " we have to thank Pr Clement and his team : they worked from noon to 8 pm. but we also have to thank everyone". They started at 8.30 am this morning putting tubes and everything to get Kamba prepared . And he stayed with his dear auntie Mavo all the operation long (which lasted 8 hours because when I called they were stil operating him). They we had Georgette and Mavo waiting for the baby to wake up.
When he awaked with his bandage on his head, he started crying which is a good sign.
We have to keep on praying for the post-operation follow-ups, Diana will of course load more pictures tomorrow  on the morning (because the connexion is  a little more better)

Bien à vous tous.

 
Please read more on :

Diana's blog : http://dianachamia.wordpress.com

the blogosphere posts http://del.icio.us/foko

Foko Blog organization http://club.foko-madagascar.org/

Who's involved? 

This great movement of solidarity started with Diana Chamia's call for help 

Jean and Bako Razafindambo came as the Black Angels who finance the trip to Antananarivo and helped with getting the surgeon contact for the medical care

Max (right) is their contact in Madagascar who is taking care of the finances and the contacts

Mr Clement (the surgeon), Madame Mavo (the family's chaperon in Antananarivo), Mme Anja Elisabeth (who is their second chaperon and providing from the donations) are people closely involved in getting Baby Kamba the good Medical cares. (more pictures online soon)

The associations and non-profit involved :

Zaza-vavy.org, for Malagasy Child and Woman, is a network of Malagasy bloggers working to protect and inform. Most of the members are actively raising funds and awareness around for Baby Kamba

Foko-Madagascar is the non-profit in charge of the media and the communication with Diana as contact, member of the Foko Blog Club from Majunga. She will be making contact with the media in town to sensibilize on her campaign.

Please find here the official list of friends and associations also promoting this cause.

You can also join us on Facebook and Follow Diana on Twitter 

17 Responses to “Help her help them : Mavo and Diana are taking good care of Georgine and Kamba”

  1. [...] Help Me Help Them by Diana Chamia [...]

  2. [...] Help Me Help Them by Diana Chamia [...]

  3. on 03 May 2008 at 11:11 ammedea

    Wow. It is sad how people turn their backs on others just because they have a malformation, or because they have problems, almost as if they thought it was contagious. I´m glad you’re helping this woman out! Keep us posted :)

  4. on 03 May 2008 at 11:24 amVictor Kaonga

    A very challenging story. So what is the progress so far? I wish her well.

  5. on 03 May 2008 at 6:44 pmikalamako

    Miss !

    http://blog.myspace.com/index.cfm?fuseaction=blog.view&friendID=211826418&blogID=389641163

    ça doit être un coup de blues à force de tourner seulement le pouce, grrr

  6. on 13 May 2008 at 4:33 amikalamako

    Bako et Jean : Go go go !
    Nous sommes avec vous tous dans le coeur ce jour-là – le coeur n’a pas de frontière. Joan est seulement notre représentante :-)
    Merci pour tous, merci merci !

  7. on 13 May 2008 at 6:00 ammaintikely

    Je n’imaginais pas que la maman était encore aussi jeune !!!

    Nous sommes tous avec vous Bako et Jean

  8. on 15 May 2008 at 4:00 pmikalamako

    merci pour les liens.
    Main dans la main izany e, izahay vonona foana !

  9. [...] led several successful digital literacy and blogger outreach campaigns, and, most recently, have raised funds for a needy and deserving family. (An interesting debate about the role of Madagascar’s diaspora community in its development [...]

  10. on 06 Jun 2008 at 3:14 amweather instrument

    Thank for Nice story.Just bookmark now!

  11. on 07 Jun 2008 at 9:52 ampissoa

    Happy Bday Baby Kamba.

    Go Diana, Foko et tout le team !!!

    U great guyzzzz.

  12. on 08 Jun 2008 at 9:41 pmfrank

    Great Information blog ! Thank you for keeping up the good work. I look forward to returning to your blog, and learning more from you !

  13. [...] She spotted a child named Kamba with an abnormal growth in the forehead and decided to help Kamba’s family to get better medical care. She appealed to the blogosphere in her blog post “help Me help them“: [...]

  14. [...] long campaign has been well documented by Foko project coordinator Joan Razafimaharo both on her personal blog and at the national blogging collective, Malagasy [...]

  15. [...] di Diana è stata assai ben documentata dal coordinatore del progetto Foko, Joan Razafimaharo, sul suo blog personale e sulla comunità nazionale Malagasy [...]

  16. [...] imeandikwa na kuorodheshwa vyema na mratibu wa mradi wa Foko, Joan Razafimaharo, kwanza katika blogu yake binafsi, na pia katika blogu ya jumuiya ya kitaifa ya wanablogu Malagasy [...]

Trackback URI | Comments RSS

Leave a Reply