Roshani |
Roshani's Award
In Roshani’s memory, Mitrataa created “Roshani’s Award”. This scholarship would be awarded to a very special young woman who had faced discrimination due to her disabilities. When we met Tulasha Poudel in her village in a remote part of Dolakha, we knew she was the perfect recipient for the first Roshani’s Award.
Meet Tulasha
Tulasha has Down’s Syndrome. She is approximately 20 years old. Her mother and sister were killed when she was about 6 years old when their house collapsed in a landslide. Her father is hearing impaired and cannot care for her. She lived with her neighbour and just sat idle at home with no support, interactions or care.
We spoke with Tulasha’s father and the community
and discussed the possibility of bringing Tulasha to Kathmandu to teach her
some life skills and independence so she can take care of herself in future.
They agreed.
Tulasha
visits Kathmandu
Initially, we brought Tulasha to Kathmandu in April
2014 for a health check-up and to see how she liked it. She came with her uncle
and father. After a successful health check-up, we gave her a bath, bought her
some new clothes and gave her some good meals. We sent them back to the village
while we worked on a solution for accommodation and support in Kathmandu.
In May 2014, Pushpa and Asbini went back to
Dolakha to check on Tulasha. The village’s attitude towards her had changed and
they were now caring for her more actively although she still needed a lot more
care and teaching to become independent.
Finding a
solution for Tulasha in Kathmandu
Tulasha with Bec and Ranju |
We needed to find a supportive, caring and
creative environment for Tulasha in Kathmandu to achieve the aims of her
scholarship – independence for her in future. We explored options in hostels in
Special Needs Schools and in the Downs Syndrome Society of Nepal. Unfortunately,
we were not confident in their ability to be able to deliver our stretching
objectives.
This process took a long time but became
particularly urgent after the earthquake in April 2015 when Tulasha’s house was
destroyed and her family had nothing left. We finally found the perfect
solution – one of our Mitrataa girl’s mother was looking for a job and she is a
natural working with disabled students. Her house had collapsed in the
earthquake and she had nowhere to stay with her 2 young children and no job. We
organised a new room for her to live in and offered to pay her rent and a
salary if she would take care of Tulasha and teach her the skills she needed to
move towards independence. We are very grateful that Babita agreed and Ashwini
went to Dolakha to bring Tulasha to Kathmandu. She will visit her family in
Dolakha a few times a year to maintain contact with them and ensure she can
return to her community in future.
Tulasha’s
journey towards independence begins
Three months have passed and Tulasha has settled
in incredibly well with Babita and her family. She has learned to bath herself,
wash her dishes and her clothes, to say her name and where she is from as well
as to greet people.
People with Down’s Syndrome are generally left in
a corner of a home with no support or opportunities in Nepal. Disabilities here
are not well understood or respected and Tulasha has been great at teaching
people that she has wonderful passion for life, an ability to learn and a huge
heart. Not only has she learned a lot, but she has taught all members of the
Mitrataa family about tolerance and understanding and we have already seen this
message being passed on to others in the extended Mitrataa family.
The road towards independence for Tulasha is long
and full of twists and turns. But she has started her journey and embraced it completely.
With Babita by her side, we are confident that in a few years, Tulasha will be
able to live independently with a support network around her.
Huge thanks to Ashwini, Bandana, and of course
Babita for their support and passion for Tulasha. We know that Roshani would be
smiling knowing that her memory lives on and has given Tulasha the opportunity for
a better future.