Rebecca in visita al Project Walk di Orlando

Quest’anno mentre ero in vacanza con la mia famiglia ho deciso di andare a visitare il centro di riabilitazione “Project Walk” di Orlando (Florida).

1 Project Walk OrlandoVolevo vedere che tipo di riabilitazione utilizzassero per aiutare le persone a rimettersi nuovamente in piedi. Seguivo infatti da qualche tempo il Project Walk tramite le notizie che apparivano principalmente on line e su Facebook e sono sempre stata interessata a capire cosa facessero davvero.

Essendo paraplegica infatti non vedo l’ora di imparare tutto ciò che può aiutarmi a tornare di nuovo come ero. A Project Walk ho trovato un clima molto incoraggiante. Ero sbalordita guardando alcuni pazienti mentre facevano esercizi che credevo, visto il tipo di lesione, non saremmo mai stati in grado di fare di nuovo, mi è sembrato semplicemente fantastico!! Il Project Walk da alle persone con Lesione Spinale speranza di recuperare utilizzando principalmente l’elettrostimolazione esterna  per promuovere la riorganizzazione del sistema nervoso in modo da far ricordare ai nervi e ai muscoli come lavorare di nuovo.3

Gli spasmi muscolari vengono utilizzati per costruire massa muscolare in modo che giochino a favore piuttosto che contro di noi.  Inoltre utilizzano un sacco di esercizi a carico naturale o con pesi leggeri e a resistenza elastica; questo di per sé favorisce la salute delle ossa. Naturalmente non dicono alle persone che saranno in grado di saltare fuori dalla sedia e uscire fuori dalla porta, ma sostengono che nel migliore dei casi il paziente sarà in grado di recuperare delle funzioni e continuare a migliorare grazie agli esercizi che permetteranno di aiutare il corpo a ricordare come muoversi.

Nei casi peggiori il paziente lascerà il centro avendo acquisito maggiore “indipendenza” perché avrà imparato ad usare al meglio le funzioni motorie residue. I benefici per la salute che si possono ottenere sono grandi e questo è qualcosa che è davvero necessario per una persona con lesione spinale.

I risultati che dicono di aver ottenuto sono:

  • Maggiore attività del sistema nervoso centrale
  • Aumento della massa muscolare
  • Aumento della circolazione
  • Aumento della sensibilità in alcuni pazienti
  • Maggiore percezione del caldo e del freddo in alcuni pazienti
  • Maggiore controllo della vita
  • Diminuzione dell’insorgere di piaghe da decubito
  • Diminuzione dell’uso di farmaci
  • Diminuzione di problemi di salute associati ad una lesione del midollo spinale
  • Speranza

2 Project Walk OrlandoQuindi questo tipo di terapia può essere un  vantaggio di tutti noi. E’ ovvio che non è una cura per la paralisi purtroppo, ma è un ottimo modo per mantenere il nostro corpo in forma, nell’attesa che i ricercatori ci diano la notizia che aspettiamo da tempo.

Come Cure Girl credo che tutti dovremmo avere la possibilità di poter accedere a questo tipo di riabilitazione per poter capire se abbiamo ancora margini di miglioramento e mantenere il nostro corpo in forma.

Vorrei ringraziare Lisa, Amanda e Brock per avere permesso a me e alla mia famiglia di visitare Project Walk.

Ci tornerò sicuramente.

Cure Girl Rebecca

Per maggiori info: http://projectwalk.com

L’Endparalysis Foundation

endparalysis foundation

In Olanda, è stata da poco presentata l’Endparalysis Foundation, una nuova interessante fondazione creata da Corinne Jeanmaire, una donna rimasta paralizzata nel 2001 a causa di un incidente stradale e che da allora si è dedicata al sostegno della ricerca di una cura per le lesioni spinali.

L’obiettivo principale della fondazione è accelerare la translazione di terapie biologiche per le lesioni spinali croniche attraverso co-finanziamenti di promettenti progetti di ricerca.

Il 100% dei fondi raccolti dalla fondazione sarà destinato alla ricerca. La Fondazione ha una solida base scientifica grazie al sostegno di esperti come il Dr. Mark Bacon, direttore scientifico alla UK International Spinal Research Trust, il Professor Jerry Silver  della Case Western Reserve University degli Stati Uniti e il Professor Joost Verhaagen dell’ Institute for Neuroscience dei Paesi Bassi.

Entro il prossimo anno, oltre alla raccolta di fondi, la fondazione mira a coinvolgere scienziati per costruire una rete di collaborazione al fine di sviluppare una roadmap flessibile per accelerare terapie combinate.

Sostenete questa nuova grande fondazione a favore di una cura visitando il loro sito web e la loro pagina facebook

Cure girl Ruth

The Endparalysis Foundation

endparalysis foundationAn exciting new cure foundation has been launched by a paralysed woman in the Netherlands. The Endparalysis Foundation has been set up by Corinne Jeanmaire, a dedicated cure advocate who was paralysed in a car accident in 2001. The Foundation’s primary goal is to accelerate the translation of biological therapies for chronic spinal cord injury by co-financing promising research projects. 100% of all funds raised by the foundation will go directly to research. The Foundation has a very strong scientific base with experts including Dr Mark Bacon, Scientific Director at the UK’s  International Spinal Research Trust, Professor Jerry Silver from Case Western Reserve University, USA and Professor Joost Verhaagen from the Netherlands Institute for Neuroscience. As well as fundraising, within the coming year foundation also aims to engage scientists build a collaborative network in order to develop a flexible roadmap for accelerating combination therapies.

Please support this great new cure foundation by having a look at the website here and liking it on facebook here.

Cure girl Ruth

CHARITY EXTRAVAGANZA NIGHT IN AID OF SPINAL RESEARCH

EXTRAVAGANZAOn Saturday 31st May my best friend Freda and I are organising a CHARITY EXTRAVAGANZA NIGHT in aid of Spinal Research. It is being held in a cool venue called Yager Bar which is in St Pauls, Central London. The tickets are £60 each and that includes admission, glass of champagne and also appetisers along with a great line up of entertainment. We are very lucky to have the help of a fantastic PR guy called Victor Trocki who has worked promoting members of the Royal family, celebrities, wag’s etc. Victor has organised many events and we really couldn’t put this together without him and are so grateful that he is really wanting to support our cause of finding a cure for spinal cord injury. We have some great acts all of which are giving their time and support free of charge. Mozez

Mozez, ex frontman of the group Zero 7 will be performing. So excited as I’m such a big fan of his and have seen him perform live… he’s amazing.

 CARLA THOMAS

Carla Thomas will be performing and she has worked with amazing artists such as Alexander O’ Neal. A very good friend of mine Carl will be doing his drag act, very funny guy along with some dancers and glamorous girls circulating the crowd. Also we have auctions and raffles with some fabulous prizes to be won. After all of the acts and auctions you’ll be able to party the night away as we also have a couple of DJ’s lined up.

Media will also be involved so hopefully good coverage in newspapers etc too. The tickets are selling fast so purchase yours now by contacting myself or Freda 07770-418-482 or you can contact Michelle Marsh directly at Spinal Research on 01483-898-786. I would like to thank everyone who is contributing to this superb evening. Both myself and Freda are so thankful for everyone’s generosity. See you on the 31st everyone for raising as much money as we possibly can to fund a cure for paralysis. Myself and the CURE GIRLS will keep on fundraising and campaigning until we can regain our independence and also WALK ONCE MORE.

From Cure Girl Lolly x

Barbara: “I THOUGHT IT WAS JUST A TEMPORARY SITUATION”

Barbara BucciRead Cure Girl Barbara’s story on Wings for Life, Spinal Cord Research Foundation website 

AN OPPORTUNITY TO SAY WE WANT A CURE!

The UK’s Stoke Mandeville Spinal Foundation (SMSF) is conducting a priority setting survey, open to individuals living with SCI and also families, carers, health and social care professionals.  This is a rare opportunity for our pro-cure voices to be heard and it’s vital that the results of this survey deliver a realistic and honest view of our desires and needs.

Surveys often ask us to prioritise our needs: “Do we want bowel and bladder? Is hand function the most important thing?” What surveys have failed to do is understand the UNDERLYING causes to all our problems: damage to the spinal cord.

 damageSo with this survey, we encourage you not to list your priorities and not to ask for a solution to symptoms but to ask a simple question:

HOW CAN WE REPAIR THE CHRONICALLY DAMAGED SPINAL CORD TO RESTORE FUNCTION?”

Care initiatives for individuals with SCI have limitations. No matter how many carers you have, how big your financial compensation package is, how light your wheelchair is, how many accessible shops and restaurants there are, how much rehabilitation is available to you, how many incontinence products available to you and how much assistive technology is available – it cannot ever compare with the gains in health, independence and wellbeing resulting from the return of function.

The repair of the chronically damaged spinal cord is the ultimate form of Quality of Life for the SCI Community!

The Cure Girls strongly urge you to take part in this survey and more importantly, ask the right question:

HOW CAN WE REPAIR THE CHRONICALLY DAMAGED SPINAL CORD TO RESTORE FUNCTION?”

 The survey is here.

Esempio

UN’OCCASIONE PER DIRE CHE VOGLIAMO UNA CURA!

La Fondazione dell’Unità Spinale di Stoke Mandeville (Regno Unito)  sta conducendo un sondaggio per definire le priorità, aperto a persone che hanno Lesioni Spinali, alle loro famiglie e agli operatori sanitari e socio assistenziali.

Questa è una rara opportunità per le nostre voci pro-cura di essere ascoltate ed è fondamentale che i risultati di questa indagine offrano una visione realistica e onesta dei nostri desideri e bisogni.

I sondaggi spesso ci chiedono di dare priorità alle nostre esigenze ad esempio:  “Vogliamo riavere l’uso dell’intestino e della vescica? La funzionalità delle mani è  la cosa più importante?”

Quello che i sondaggi non sono riusciti a fare é comprendere  la causa alla base di tutti i nostri problemi: il danno al midollo spinale!

 damage

Quindi, con questa indagine, vi consigliamo di non elencare le vostre priorità, non chiedere cioè una soluzione per i sintomi, ma porre una semplice domanda:

“COME POSSIAMO RIPARARE UNA LESIONE SPINALE CRONICA E RIPRISTINARE TUTTE LE FUNZIONI? “

Purtroppo tutte le Iniziative di assistenza per le persone con lesione spinale hanno dei limiti. Non importa quante badanti hai, quanto è grande il tuo pacchetto azionario, quanto è leggera  la tua carrozzina, che ci siano un sacco di prodotti per l’incontinenza, quanti negozi e ristoranti accessibili ci sono, quanta riabilitazione hai a disposizione, e quanta tecnologia sia disponibile;

Nulla potrà mai essere paragonato al  guadagno in salute, indipendenza e benessere derivante dal ritorno delle funzioni!!!

La riparazione delle lesioni spinali croniche è  la forma più totale di miglioramento della qualità della vita per le persone mielolese!

Le Cure Girls vi consigliano vivamente di prendere parte a questo sondaggio e, soprattutto, porre la giusta domanda :

“HOW CAN WE REPAIR THE CHRONICALLY DAMAGED SPINAL CORD TO RESTORE FUNCTION?”

Cliccate qui per accedere al sondaggio inglese  e completate come da esempio

Esempio

Cure Girls: “Actions, not just words!”

 
 
Actions, not just words
 
 
Hey Everyone,
 
lots of VERY exciting things planned for us in the next few months ahead.Cure Girl Rebecca will be competing in the last part of the Jersey marathon in October and raising all funds for Unite 2 Fight Paralysis.Italian Cure Girls will be organising Ride For Life 2013 in Italy [ Pista South Milano di Ottobiano (PV) ] .

Cure Girl Ruth has also something yet to be revealed!!!!

Cure Girl Lolly will be visiting the Miami Project later in the year to discuss CURE with the researchers and also planning a Charity Cabaret Gala in London with her dear friend Mark raising all money for Spinal Research.

We will be releasing specific dates/sponsorship details ASAP.

Keep spreading the love and sharing our Cure Girls FB Fan Page to let everyone know OUR and YOUR mission TO MAKE CHRONIC SPINAL CORD INJURY CURABLE.

Have a great day all!!!!! 

Love from the CURE GIRLS X

 

The realities of spinal cord injury are far more complex than just “not walking”.

The realities of Spinal Cord Injury are far more complex than just not walking. When someone becomes paralysed, they are unable to coordinate the complex signals needed up and down the spinal cord to undertake urination. The bladder becomes paralysed and individuals with SCI are often unable to tell when they need to urinate and almost all paralysed people are unable to go to the bathroom without the use of catheters, other pieces of equipment and extensive use of pharmaceuticals to assist with bladder spasms.

bladders/catheterisationAny form of catheterisation causes significant health problems for paralysed individuals as it enables the introduction of microscopic bacteria directly into the bladder, resulting in complex urinary tract infections (UTIs). In paralysed individuals, UTIs cause a significant increase in painful spasms and spasticity all over the body but also in the bladder itself, causing leakage of urine. UTIs are often accompanied by fever, chills and debilitating fatigue, all of which severely impact the paralysed individual’s ability to lead an independent and fulfilling life. Untreated, UTIs can lead to further medical complications, hospitalisation and even death caused by sepsis.

Paralysed people have no other available alternative methods to urinate and therefore must use catheters despite their inherent risks. The best care in the world will not prevent bacterial colonisation of the paralysed bladder; care can only mask the symptoms. To deal with the problem, we need cure.

Silver and Lee

Thankfully, those in the field of regenerative medicine are moving towards a solution. This week saw the publication of an article by Dr Jerry Silver and team in the Journal of Neuroscience entitled ‘”Nerve Regeneration Restores Supraspinal Control of Bladder Function after Complete Spinal Cord Injury”. Although still in early, animal stages this is great news for those relying on catheters.

Hope is here, and change is on the horizon!

Cure Girls

$20m Wasted on Anniversary Celebrations: Why it’s time for leadership change at the Rick Hansen Foundation

Rick Hansen - Man in Motion25 years ago, Rick Hansen completed his ‘Man in Motion’ World Tour – a trans-global wheelchair push-fest to raise money for research and those living with spinal cord injury. To celebrate this anniversary (and Rick’s continued standing as a Canadian hero), the Rick Hansen Foundation (RHF) has recently celebrated the 25th anniversary. A scathing article “Behind the Rick Hansen Foundation” in Canada’s The Star Phoenix newspaperoffers us an interesting insight into where this organisation gets its money from and how it spends it. Prepared to be shocked!

Seasoned cure campaigners, will be familiar with the Rick Hansen Foundation (RHF). In 2011/12, cure activists launched a campaign which aimed to find out what percentage of funding RHF was spending on a cure for chronic spinal cord injury (SCI). Despite hundreds of supporters’ requests for transparency through several email campaigns, RHF refused to be open about what they were spending their millions on. Talks eventually broke down and activists were dismissed with well-meaning but essentially empty rhetoric about the need for collaboration and the importance of care.

David Baines June 22nd article in The Star Phoenix supports what advocates have long suspected – there is no coherent strategy is place to ensure chronic SCI becomes curable. What’s worse is that this organisation is eating the lion’s share of funding and there is no accountability to those it purportedly serves.

The table below summarises the total cost of the anniversary expenditure, estimated to be in the region of $17m – $19m (Canadian dollars). Some could argue that to make money you have to spend money, but as we shall see later, expenditure for the celebrations far out-weighed any revenues generated by the anniversary celebrations.

Activity  Cost
Cross-Canada Relay $10.94m
Homecoming Gala $1.95m
International Conference $1.44
“International Outreach” Programme £1.27m
“Planat” – online accessibilities rating tool $1.1m
Total Anniversary Expenditure $17m -$19m

Let’s look specifically at what the money for the celebrations was spent on. The largest expenditure, costing nearly $11m was the cross-Canada relay which retraced Hansen’s original route. No expense was spared for this and instead of using a torch, participants received specially made ‘Rick Hansen Medals’. The celebrity-studded ‘Homecoming Gala’ weighed in $1.95m and generated only $274,572, resulting in a net loss of $1.67m. RHF staged an international conference in Vancouver as part of these anniversary celebrations, the aim of which was to share ‘best practices for spinal cord research and care’. Costing $1.44m and generating only $200,600 it resulted in another net loss of $1.24m.

Other anniversary celebrations included an “International Outreach Programme” which saw Hansen and his team go on a global tour, the aim of which was to further collaboration on spinal cord research and care. The cost for this came in a $1.27m and as there were no measurable outcomes it’s difficult to evaluate if this programme was value for money.

The anniversary celebrations also saw the launch of “Planat” – an online ratings tool that enables users to rate the accessibility of buildings and public spaces. It’s apparently being well received but software specialists have queried the cost; a hefty $1.11m.

RHF has failed to recoup any of its anniversary expenditure through revenues as the Foundation made a large miscalculation regarding how much they thought the celebrations would generate. The goal was to raise $250m in donations and future commitments but as the table below shows only $84m has been secured, a majority of which is tax-payer money.

Source  Amount
Government grants, corporate contributions & sponsorships that were received and spent during the anniversary campaign $23.3m
Provincial Gov’t funding for the BC Neuro-trauma Fund (Not new funding, to be spread over 5 years) $10m
Provincial Gov’t funding for Rick Hansen Institute (Not new funding, to be spread over 7 years) $11
Federal Ministry of Western Economic Diversification (WED) (last tranche of a $13.5m, three-year funding agreement) $4.5
Federal Ministry Western Economic Diversification (WED) (to be spread over five years) $35m
 “Alberta government repurposing” $500,000
Total revenue generated during anniversary celebrations $83.3m

So, were the celebrations worth it? It would appear that a majority of the generated income would have been donated regardless of the anniversary celebrations, rendering anniversary expenditure increasingly difficult to justify. RHF has countered this argument by suggesting that one of the primary goals of the anniversary celebrations was to ‘raise awareness’. Again, with no measurable targets or outcomes, it’s anyone’s guess if this goal has been met.

RHF expected revenues to be greatly boosted by the anniversary celebrations but, as the table below shows, there were no significant increases in total revenue.

Year Ending Total Revenues
31st March 2010 (the year prior to the tour launch) $24.9m
31st March 2011 (during tour) $22.4m
31st March 2012 (during tour) $27.2m

And it’s not just the anniversary celebrations that are raising questions about financial leadership at RHF. The article raises questions about a lack of commitment to financial transparency, unethical financial practices regarding taxes and unjustified and secretive compensation packages.CANADIAN PUBLIC RELATIONS SOCIETY - The Canadian Public Relation

The Foundation argues that the investment of $17m – $19m in the anniversary celebrations was calculated, insisting that it was a strategic investment to capitalise on a one-time opportunity. However, the figures speak for themselves; it was a gamble to invest so much in the anniversary celebrations and it clearly hasn’t paid off. The anniversary celebrations can only be seen for what they really are: a huge waste of desperately needed funds.

Stay tuned to Cure Girls, StemCells&AtomBombs and CareCure to find out how you can help address the mismanagement of desperately needed funding.

Cure Girl Ruth