NO ONE SHOULD FACE MS ALONE!
Can you imagine waking up one day unable to do the everyday things you would usually take for granted? Like not being able to see properly (or at all), unable to get out of bed, walk to the phone to call someone – anyone – or live a life without pain?
All of a sudden, your world has changed.
Multiple sclerosis is a chronic and often debilitating disease which attacks the central nervous system (the brain, spinal cord and optic nerves). It is the most common neurological disease in young adults and often attacks people at a time in their lives when they are planning families and building a career. Three out of four people living with MS are women.
With your support, we can allow people living with multiple sclerosis access to vital support services, like MS Connect, MS Peer Support and MS Employment Support Programs. We’ll also be helping bring new treatments closer to reality, investing in repairing myelin damage to restore function that has been lost for people with progressive forms of the disease.
On behalf of over 33,300 Aussies living with multiple sclerosis – THANK YOU FOR YOUR SUPPORT!
My Updates
Together anything is possible.
Saturday 22nd Feb 𝙊𝙣𝙘𝙚 𝙖 𝙮𝙚𝙖𝙧 𝙄 𝙩𝙖𝙠𝙚 𝙥𝙖𝙧𝙩 𝙞𝙨 𝙖𝙣 𝙚𝙫𝙚𝙣𝙩 𝙩𝙝𝙖𝙩 𝙄 𝙝𝙤𝙡𝙙 𝙨𝙤 𝙘𝙡𝙤𝙨𝙚 𝙢𝙮 𝙝𝙚𝙖𝙧𝙩. 𝙏𝙝𝙞𝙨 𝙚𝙫𝙚𝙣𝙩 𝙞𝙨 𝙖𝙗𝙤𝙪𝙩 𝙖𝙘𝙠𝙣𝙤𝙬𝙡𝙚𝙙𝙜𝙞𝙣𝙜 𝙖𝙣𝙙 𝙗𝙧𝙞𝙣𝙜𝙞𝙣𝙜 𝙖𝙩𝙩𝙚𝙣𝙩𝙞𝙤𝙣 𝙩𝙤 𝙩𝙝𝙤𝙨𝙚 𝙬𝙝𝙤 𝙝𝙖𝙫𝙚 𝙨𝙤𝙢𝙚𝙩𝙝𝙞𝙣𝙜 𝙠𝙣𝙤𝙬𝙣 𝙖𝙨 𝙩𝙝𝙚 𝙞𝙣𝙫𝙞𝙨𝙞𝙗𝙡𝙚 𝙙𝙞𝙨𝙚𝙖𝙨𝙚. 𝙈𝙪𝙡𝙩𝙞𝙥𝙡𝙚 𝙎𝙘𝙡𝙚𝙧𝙤𝙨𝙞𝙨 (𝙈𝙎) 𝙞𝙨 𝙤𝙛𝙩𝙚𝙣 𝙘𝙖𝙡𝙡𝙚𝙙 𝙩𝙝𝙚 "𝙞𝙣𝙫𝙞𝙨𝙞𝙗𝙡𝙚 𝙙𝙞𝙨𝙚𝙖𝙨𝙚" 𝙗𝙚𝙘𝙖𝙪𝙨𝙚 𝙢𝙖𝙣𝙮 𝙤𝙛 𝙞𝙩𝙨 𝙨𝙮𝙢𝙥𝙩𝙤𝙢𝙨, 𝙡𝙞𝙠𝙚 𝙛𝙖𝙩𝙞𝙜𝙪𝙚, 𝙘𝙤𝙜𝙣𝙞𝙩𝙞𝙫𝙚 𝙙𝙞𝙛𝙛𝙞𝙘𝙪𝙡𝙩𝙞𝙚𝙨, 𝙥𝙖𝙞𝙣, 𝙖𝙣𝙙 𝙨𝙚𝙣𝙨𝙤𝙧𝙮 𝙞𝙨𝙨𝙪𝙚𝙨, 𝙖𝙧𝙚 𝙣𝙤𝙩 𝙧𝙚𝙖𝙙𝙞𝙡𝙮 𝙫𝙞𝙨𝙞𝙗𝙡𝙚 𝙩𝙤 𝙤𝙩𝙝𝙚𝙧𝙨, 𝙢𝙚𝙖𝙣𝙞𝙣𝙜 𝙥𝙚𝙤𝙥𝙡𝙚 𝙬𝙞𝙩𝙝 𝙈𝙎 𝙢𝙞𝙜𝙝𝙩 𝙖𝙥𝙥𝙚𝙖𝙧 𝙤𝙪𝙩𝙬𝙖𝙧𝙙𝙡𝙮 𝙝𝙚𝙖𝙡𝙩𝙝𝙮 𝙚𝙫𝙚𝙣 𝙬𝙝𝙚𝙣 𝙚𝙭𝙥𝙚𝙧𝙞𝙚𝙣𝙘𝙞𝙣𝙜 𝙨𝙞𝙜𝙣𝙞𝙛𝙞𝙘𝙖𝙣𝙩 𝙨𝙮𝙢𝙥𝙩𝙤𝙢𝙨, 𝙡𝙚𝙖𝙙𝙞𝙣𝙜 𝙩𝙤 𝙖 𝙥𝙚𝙧𝙘𝙚𝙥𝙩𝙞𝙤𝙣 𝙩𝙝𝙖𝙩 𝙩𝙝𝙚𝙮 𝙖𝙧𝙚 𝙣𝙤𝙩 𝙩𝙧𝙪𝙡𝙮 𝙨𝙞𝙘𝙠. 𝙃𝙖𝙫𝙞𝙣𝙜 𝙈𝙎 𝙞𝙨 𝙘𝙝𝙖𝙡𝙡𝙚𝙣𝙜𝙞𝙣𝙜, 𝙗𝙪𝙩 𝙢𝙮 𝙛𝙚𝙡𝙡𝙤𝙬 𝙬𝙖𝙧𝙧𝙞𝙤𝙧𝙨 𝙠𝙣𝙤𝙬 𝙩𝙝𝙖𝙩 𝙤𝙪𝙧 𝙗𝙪𝙧𝙙𝙚𝙣 𝙤𝙛𝙩𝙚𝙣 𝙗𝙧𝙞𝙣𝙜𝙨 𝙤𝙪𝙩 𝙩𝙝𝙚 𝙗𝙚𝙨𝙩 𝙞𝙣 𝙪𝙨 — 𝙘𝙤𝙪𝙧𝙖𝙜𝙚, 𝙚𝙢𝙥𝙖𝙩𝙝𝙮, 𝙖𝙣𝙙 𝙧𝙚𝙨𝙞𝙡𝙞𝙚𝙣𝙘𝙚. 𝙋𝙡𝙚𝙖𝙨𝙚 𝙨𝙝𝙖𝙧𝙚, 𝙙𝙤𝙣𝙖𝙩𝙚, 𝙟𝙤𝙞𝙣 𝙤𝙧 𝙖𝙡𝙡 3. 𝙈𝙖𝙮𝙗𝙚 𝙤𝙣𝙚 𝙙𝙖𝙮 𝙩𝙝𝙚𝙧𝙚 𝙬𝙞𝙡𝙡 𝙗𝙚 𝙖 𝙘𝙪𝙧𝙚 𝙗𝙪𝙩 𝙪𝙣𝙩𝙞𝙡 𝙩𝙝𝙚𝙣 𝙬𝙚 𝙛𝙞𝙜𝙝𝙩. 💪Share
