Please consider donating to fund crucial gene therapy research for my sweetest nephew Austin, who has a rare, fatal form of congenital (ie present at birth) muscular dystrophy (CMD). 100% of funds are going to urgently fund a research project with a major academic institution. Let’s save Austin and other children with LMNA related muscular dystrophies. We are ready to start the research as soon as we meet our goal of $2 million. It is doable with YOUR support! ❤️
L-CMD Research Foundation x 2025
Raising $ and awareness for rare disease treatments for kids impacted by terminal L-CMD, like Austin.
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Organized by L-CMD Research Foundation
Mariel Borrel
Fundraiser since Feb 2021
$3,541
41 supporters
7% of $50,000 goal
Mariel Borrel's Story
Team Leaderboard
1
Hannah + Friends
23 members
$310,101
2
BMS '01
25 members
$179,736
3
Team Mercy
2 members
$140,160
4
The LOWE Family et al
3 members
$69,305
5
4Austin
8 members
$55,511
6
CD friends
2 members
$49,750
7
Bellezzas & friends
4 members
$39,671
8
Mike Borrel et al
13 members
$33,368
9
Theta Kites + Friends
18 members
$28,441
raised of $50,000 goal
10
Friends of BMS 03
26 members
$19,440
11
Michelle + Louise
6 members
$17,748
12
Mariel’s Squad Goals
13 members
$14,279
13
Angela/Donny/NYC crew
3 members
$11,015
14
MD HFMA Friends
1 member
$8,955
15
Lauren Cox's Team
2 members
$4,570
16
Alice & friends
1 member
$4,545
17
Lynette Borrel & Crew
6 members
$3,581
18
U of MD Smith
2 members
$3,350
19
Amy & Lauren AUS
3 members
$3,100
20
Appelbaum Training Institute
1 member
$2,815
21
BMS Alumnae Board Past & Present
3 members
$2,514
22
Mighty Mindful
2 members
$1,630
23
Liz Potarazu
1 member
$1,425
24
Casual Carats
1 member
$1,015
25
Gretchen and Ryan
1 member
$600
26
Nithin Nallapati + Friends
1 member
$285
27
Alli Carlock & Friends
1 member
$250
28
Curate Capital
1 member
$0
29
Grace D
1 member
$0
