"We need a representative who is passionate about change. You're that person!"
Sabrina Ferris
"I've worked closely with Cllr Francis Timmons many times, and he always comes from a strong social justice perspective. He's extremely hard working, passionate. We need strong Independent voices like Francis in our Councils and local authorities."
Senator Frances Black - Independent
"I am glad that a person of such integrity is going forward for public office."
Jim Jackman (Former President of the National Parents Council PP)
"He has inspired many people first hand and nothing ever seems to stop him promoting fairness and equality!"
Shonach Hanaphy
"It is a breath of fresh air to have a man such as yourself represent the forgotten public. With your years of first hand experiences, kindness and your courage to ask the right questions to the right people."
Margaret Kerslake
“Francis is an exemplary public representative deeply embedded in his community and wider constituency. The energy that he brings to his community and voluntary work is breath-taking and humbling.”
Senator Gerard Craughwell
“A lot of what Francis does goes unseen and unreported but not unappreciated by the countless people he has helped and represented. Everything he does is framed by his long standing commitment to equality, inclusion and social justice. He truly is a politician for the people.”
Senator Gerard Craughwell
"Think you are a great independent voice for the people in Clondalkin."
Ann Reynolds
"Francis is very proactive within our community, will always follow up on your quires and mainstains clear communications at all times"
Jakki Byrne - Cherrywood
"if you need a voice on SDCC vote for Francis Timmons #1"
Mike Lowry - Newcastle
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As Dublin West Brendan Kenna Branch Chairperson I am delighted to have played a part in this.

I welcome the news that that the HSE will reimburse Fampyra or Fampridine in cases where people with MS ‘satisfy a responder protocol’ and have been prescribed the drug by a healthcare professional. Fampyra, an oral drug used for the symptomatic treatment of walking impairment in adults with MS will be available under the HSE General Medical Services (GMS) Scheme from today, October 1st 2015.

Monday, March 09, 2015

MOTION NO. 15

MOTION: Councillor F. Timmons

For people living with Multiple Sclerosis, in regard to the medication Fampyra early in 2013, notification was given by the HSE that the drug would not be reimbursed. While this life changing Medication is fully available, any patients wishing to receive treatment will be required to either make alternative funding arrangements or to self-fund their treatment. This Council supports the introduction of availability of this Medication to all in need regardless of ability to pay, and calls on the Minister for Health, the Government and the HSE to reverse this decision.

Some good news for people living with MS – The HSE said it expects to confirm the reimbursement date soon. It pointed out that it will repay the cost of the drug where people with MS have responded positively to the drug. Since July last year, Fampyra has only been available to people with multiple sclerosis who can afford to pay for it.

My Motion for April County Council meeting ”For people living with Multiple Sclerosis, in regard to the medication Fampyra early in 2013, notification was given by the HSE that the drug would not be reimbursed. While this life changing Medication is fully available, any patients wishing to receive treatment will be required to either make alternative funding arrangements or to self-fund their treatment.  This Council supports the introduction of availability of this Medication to all in need regardless of ability to pay, and calls on the Minister for Health, the Government and the HSE to reverse this decision. ”

Cllr Francis Timmons (independent) and Chairman of the Dublin West Brendan Kenna MS Ireland branch welcomes the HSEs decision to reimburse the Fampyra drug for people with Multiple Sclerosis. Fampridine PR or Fampyra is a slow-release oral tablet developed for people with all types of MS to improve walking ability. Cllr Timmons said this medication has the potential to increase many peoples independence and increase there quality of life.

Cllr Timmons said ”The cost of this medication is to costly for many and therefore many cannot benefit from the medication. It is disgraceful People with multiple sclerosis have had to pay up to €500 a month for a drug that could help them walk, this news is very welcome.

Multiple Sclerosis is a progressive neurological condition that affects the motor, sensory and cognitive functioning of the body. It usually develops between the ages of 20 and 40 and more than twice the number of women than men are affected. Eight thousand people and their family members live with Multiple Sclerosis across Ireland. Although MS is a progressive neurological condition that can affect a person’s health, lifestyle and relationships many people with MS find ways to manage and cope with many of the affects and difficulties.

Living from day-to-day with MS is a combination of many things: *Medically, it is about working with health professional to find suitable treatments and interventions that can keep you healthy. *Socially, it is about finding ways to maintain participation in society through your home life, work, leisure pursuits and community activity. *Emotionally, it is about finding ways to cope with challenges and maintain good mental health.

Cllr Timmons also welcomes decision by The Department of Health to introduce regulations that have enabled authorized, cannabis-based medical products such as Sativex to be legally prescribed by medical practitioners and used by patients. This will provide many benefits for many. Sativex has been proven to have benefits in treating spasticity in MS. People with MS should have the choice to use and benefit from this treatment to assist them manage the affects spasticity may have to their life. spasticity can include “tightness”, stiffness, or “pull” of muscles.

Cllr Timmons said ”The Dublin West Brendan Kenna MS Ireland branch is always looking for funds , we accept any donations monetary or that can be used as prizes for fundraisers. You can contact me @ 087 286 9315 or email ftimmons@cllrs.sdublincoco.ie ”

We are holding a fundraiser on 25th September @ 8pm in the Waterside pub function room cost €10- each a night of psychics and mediumship to raise funds for the branch.

My Motion for April County Council meeting ”For people living with Multiple Sclerosis, in regard to the medication Fampyra early in 2013, notification was given by the HSE that the drug would not be reimbursed. While this life changing Medication is fully available, any patients wishing to receive treatment will be required to either make alternative funding arrangements or to self-fund their treatment.  This Council supports the introduction of availability of this Medication to all in need regardless of ability to pay, and calls on the Minister for Health, the Government and the HSE to reverse this decision. ”

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Cllr Francis Timmons (independent) and Chairman of the Dublin West Brendan Kenna MS Ireland branch is calling on the HSE to reimburse the Fampyra drug for people with Multiple Sclerosis. Fampridine PR or Fampyra is a slow-release oral tablet developed for people with all types of MS to improve walking ability. Cllr Timmons said this medication has the potential to increase many peoples independence and increase there quality of life.

Cllr Timmons said ”The cost of this medication is to costly for many and therefore many cannot benefit from the medication. It is disgraceful People with multiple sclerosis have to pay up to €500 a month for a drug that could help them walk , The HSE has confirmed Fampyra is not covered under any of its community drugs schemes.”

Multiple Sclerosis is a progressive neurological condition that affects the motor, sensory and cognitive functioning of the body. It usually develops between the ages of 20 and 40 and more than twice the number of women than men are affected. Eight thousand people and their family members live with Multiple Sclerosis across Ireland. Although MS is a progressive neurological condition that can affect a person’s health, lifestyle and relationships many people with MS find ways to manage and cope with many of the affects and difficulties.

Living from day-to-day with MS is a combination of many things:
*Medically, it is about working with health professional to find suitable treatments and interventions that can keep you healthy.
*Socially, it is about finding ways to maintain participation in society through your home life, work, leisure pursuits and community activity.
*Emotionally, it is about finding ways to cope with challenges and maintain good mental health.

Cllr Timmons also welcomes decision by The Department of Health to
introduce regulations in the coming weeks which will enable authorised, cannabis-based medical products such as Sativex to be legally prescribed by medical practitioners and used by patients. This will provide many benefits for many. Sativex has been proven to have benefits in treating spasticity in MS. People with MS should have the choice to use and benefit from this treatment to assist them manage the affects spasticity may have to their life. spasticity can include “tightness”, stiffness, or “pull” of muscles.

Cllr Timmons said ”The Dublin West Brendan Kenna MS Ireland branch is always looking for funds , we accept any donations monetary or that can be used as prizes for fundraisers. You can contact me @ 087 286 9315 or email ftimmons@cllrs.sdublincoco.ie ”

World MS Day takes place on 27th May 2015 and you are welcome to join us as we mark this day and remember deceased members of the Brendan Kenna Dublin West MS Ireland Branch by releasing balloons from the Car Park in the Waterside Pub @ 8pm. Light refreshments will be served afterwards. Let us know if you can attend.

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We need committee members please contact me if you are interested.

The Brendan Kenna West Dublin MS Ireland Branch Annual General Meeting takes place on:

Date: Wednesday 29th April 2015 
Time: 8pm
Venue: Waterside Pub, Clondalkin

1236563_10151694238509150_1392527407_n

Cllr Francis Timmons (independent) and Chairman of the Dublin West Brendan Kenna MS Ireland branch is calling on the HSE to reimburse the Fampyra drug for people with Multiple Sclerosis. Fampridine PR or Fampyra is a slow-release oral tablet developed for people with all types of MS to improve walking ability. Cllr Timmons said this medication has the potential to increase many peoples independence and increase there quality of life.

Cllr Timmons said ”The cost of this medication is to costly for many and therefore many cannot benefit from the medication. It is disgraceful People with multiple sclerosis have to pay up to €500 a month for a drug that could help them walk , The HSE has confirmed Fampyra is not covered under any of its community drugs schemes.”

Multiple Sclerosis is a progressive neurological condition that affects the motor, sensory and cognitive functioning of the body. It usually develops between the ages of 20 and 40 and more than twice the number of women than men are affected. Eight thousand people and their family members live with Multiple Sclerosis across Ireland. Although MS is a progressive neurological condition that can affect a person’s health, lifestyle and relationships many people with MS find ways to manage and cope with many of the affects and difficulties.

Living from day-to-day with MS is a combination of many things:
*Medically, it is about working with health professional to find suitable treatments and interventions that can keep you healthy.
*Socially, it is about finding ways to maintain participation in society through your home life, work, leisure pursuits and community activity.
*Emotionally, it is about finding ways to cope with challenges and maintain good mental health.

Cllr Timmons also welcomes decision by The Department of Health to
introduce regulations in the coming weeks which will enable authorised, cannabis-based medical products such as Sativex to be legally prescribed by medical practitioners and used by patients. This will provide many benefits for many. Sativex has been proven to have benefits in treating spasticity in MS. People with MS should have the choice to use and benefit from this treatment to assist them manage the affects spasticity may have to their life. spasticity can include “tightness”, stiffness, or “pull” of muscles.

Cllr Timmons said ”The Dublin West Brendan Kenna MS Ireland branch is always looking for funds , we accept any donations monetary or that can be used as prizes for fundraisers. You can contact me @ 087 286 9315 or email ftimmons@cllrs.sdublincoco.ie ”

Today i think of all people living with Multiple Sclerosis. Today is World MS day. The Dublin West ‘Brendan Kenna’ Branch is holding a Balloon Launch @ 8pm at the Waterside tonight to mark World MS Day.

The Dublin West Brendan Kenna MS Ireland Branch was delighted with the turnout and support for the Branch on Saturday 24th. The Branch along with Bawnogue youth and community centre and Action Community Enterprise centre had a fun filled day that managed to raise much needed awareness of MS.

Press Release:
The Dublin West MS Ireland ‘’Brendan Kenna’’ Branch will hold a Family day with the Bawnogue youth and Community centre on the 24th August from 1-5. The Family day will also aim to raise funds for the local branch and raise the profile of MS in the Dublin West area.

Eight thousand people and their family members live with Multiple Sclerosis across Ireland.  Although MS is a progressive neurological condition that can affect a person’s health, lifestyle and relationships many people with MS find ways to manage and cope with many of the affects and difficulties. The Branch support people with MS in the Dublin West area.

We are grateful for the help of K & G Fun Fair , All Dublin Bouncing castles , Partyworld , Professor Sneedypoppers , Gerard Kinsella DJ , Dublin Fire Brigade , Eddie Kinsella Photographer etc also we wish to thank our sponsors Coca Cola , Robert Roberts , Dunes Stores , Top Flight and all other donators.

We will also have Mickey and Minnie mouse attending.

Please contact Francis Timmons Branch Chairman – 087 286 9315 or email info@francistimmons.com if you can help in any way or require any further information.

 

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