Member Comments are provided by individuals and reflect their personal opinions only. Under NO circumstances should you act on any advice or opinion posted in this forum.  ALWAYS check with your personal physician before taking any action regarding your health! MedHelp International and our partners, sponsors and affiliates have no obligation to monitor any comments posted on this site, or the content and/or accuracy of such exchanges. MedHelp International does not endorse the views of any user.
 | 

Off Topic

by FLBrat, Sep 12, 2007 06:54AM
If anyone has information on Familial ALS, can you help my friend out on the ALS board??  Thanks
Member Comments (3)

by Celeste77, Sep 12, 2007 09:48AM
To: FLBrat
I'm so sorry to hear about your friends loved one. Unfortunetly I have lost a loved one due to this hideous disease. I posted the same info under the post "Anyone have experience with FALS?" by jcarnahan, hopefully it is the right post. If not, perhaps you can pass this on?..

The ALS Association website is a good place to start. It offers state to state ALS centers, programs etc. facts, latest news, and various support referrals.
http://www.alsa.org/faq/community.cfm?CFID=3375601&CFTOKEN=13355385
You can contact them directly:
The ALS Association, National Office
Phone: @(818) 880-9007
Fax:     @(818) 880-9006

Family Caregiver Alliance
A valuable resource for family members of ALS patients, the Family Caregiver Alliance specializes in nervous system disorders, including ALS. In addition to maintaining a network of resource centers, this organization sponsors education and training workshops, respite programs, support groups, and conferences. It also conducts consultations on the telephone and offers information and referrals.
(FCA)
http://www.caregiver.org


Caregiver/Family
The National Caregivers Association offers support and education for the 20 to 30 million people throughout the United States who provide care for a loved one. The association does not specialize in nervous system disorders, but provides caregiver support for a variety of conditions, including ALS. It recently conducted a member survey to determine the top concerns of caregivers, distributing information to members in the form of reports and through its newsletter. In addition, a peer-to-peer networking program helps families dealing with the same disease or with similar circumstances, establish contact with each other. In this way, families can share experiences and exchange valuable information.

National Family Caregivers Association (NFCA)
10400 Connecticut Avenue, Suite 500
Kensington, MD 20895-3944
Phone: @(800) 896-3650 or @301-942-6430
Fax: @301-942-2302
http://www.nfcacares.org/


The National Alliance for Caregiving is dedicated to providing support to family caregivers and the professionals who help them and to increasing public awareness of issues facing family caregivers.
http://www.caregiving.org/

by FLBrat, Sep 12, 2007 11:07AM
Thanks Celeste

by Celeste77, Sep 12, 2007 08:28PM
To: FLBrat
Your welcome..hope it helps some and I hope your doing well.
Related discussions
Post Comment
To
Comment
Post Comment
Recent Activity
JenB12 commented on Simple tool to Assess...
6 hrs ago
April2 commented on please all of cheri's...
7 hrs ago
LindaTX commented on photo
7 hrs ago
cece68 added the Food Diary
7 hrs ago
Jade59 commented on photo
7 hrs ago
LindaTX commented on photo
8 hrs ago
LindaTX commented on photo
8 hrs ago
Lechsa added the Exercise Tracker
8 hrs ago
RSS Expert Activity
EVIDENCE-BASED APPROACH TO NEUTER S...
22 hrs ago by Arnold L Goldman, D.V.M.
HOW DO/SHOULD DOCTORS THINK ABOUT T...
22 hrs ago by Arnold L Goldman, D.V.M.
Simple tool to Assess your Risk for...
Dec 14 by Lee Kirksey, MD
Community Members