Reviews
Would you recommend Multiple Sclerosis Association of America (MSAA)?
47 reviews
Write a review
Write a review
(August 14, 2024)
Last year, my 68-year-old partner was diagnosed with Lou Gehrig's disease also known as ALS. Speaking and swallowing were two of his challenges. His collapse was swift and catastrophic, and neither the riluzole nor the medical staff did much to aid him. He would not have survived if our primary care physician hadn't given him attentive care and attention, as the hospital center didn't provide any psychological support. His fall was abrupt and catastrophic. His hands and legs gave way to weakness in his arms. This year our family physician suggested using vinehealthcentre. com ALS/MND treatment, which my husband has been receiving for a few months now. I'm delighted to say that the treatment greatly reduced and reversed his symptoms of ALS, he no longer requires a feeding tube, sleeps soundly, works out frequently, and is now very active. In the hopes that it could be useful, I thought I would relate my husband's tale; in the end, you have to do what suits you the best.
(July 25, 2024)
Using herbal natural remedy was what got me tested negative to HSV 2 after being diagnosed for years. I have spent so much funds on medications like acyclovir (Zovirax), Famciclovir (Famvir), and Valacyclovir (Valtrex). But it was all a waste of time and my symptoms got worse. To me It is very bad what Big pharma are doing, It’s also crucial to learn as much as you can about your diagnosis. Seek options:( worldrehabilitateclinic. com ).
(March 22, 2024)
Sending you prayers, I was diagnosed with multiple sclerosis 1 month after I turned 45. My grandma is 96 and had it since she was in her 20s. I have been on Copaxone, the first year was daily and now I am on 40 mg, 3 times a week. It made a tremendous difference for me. Although the fatigue is what really gets to me. When I do too much, I do start to feel weak. My MS got significantly worse and unbearable I decided to quit my meds due to side effects. Our care provider introduced me to Ayurvedic treatment. I had a total decline of all symptoms including vision problems, numbness and others. Sometimes, i totally forget i ever had MS. Visit Natural Herbs Centre web-site naturalherbscentre. com. I am very pleased with this treatment. I eat well, sleep well and exercise regularly. God bless all MS Warriors
(November 13, 2023)
Genital herpes and PTSD have affected my life, perspective, and hobbies greatly and I have learned to make this vice into one of my greatest virtues all thanks to ‘Molemen Herbs’ on Facebook and YouTube as they directed me on how to reverse and cure my herpes diagnosis permanently with natural herbal medicines which helped me to improve my focus, changed my mindset, and also helped me provide insight into who I am, and how I grew as a person, y'all should check them out on Facebook, they are the best herbal healers to help you cure any diseases or health conditions. You can connect with ‘Molemen Herbs’ on Facebook or YouTube.
(March 17, 2023)
My husband was diagnosed of Parkinson's disease 2 years ago, when he was 49. He had a stooped posture, tremors, right arm does not move and also a pulsating feeling in his body. He was placed on Sinemet for 8 months and then Siferol was introduced and replaced the Senemet, during this time span he was also diagnosed with dementia. He started having hallucinations, lost touch with reality. Suspecting it was the medication I took him off the Sifrol (with the doctor’s knowledge) and started him on PD natural herbal formula we ordered from Health Care HERBAL CENTRE, his symptoms totally declined over a 3 weeks use of the Health Care HERBAL Parkinson's disease natural herbal formula. He is now almost 51 and doing very well, the disease is totally reversed! Visit w w w. healthcareherbalcentre .com
(April 25, 2022)
I was diagnosed in 1986, before symptoms started. I am a pianist, suddenly unable to open my hands wide enough to get 8 keys. Nobody in my family had MS, nor my grandparents. Last year a cousin younger than me had MS, she is 40. I have primary progressive MS. I do not walk for the last 18 years, I was born in 1952. I have had 6 strokes and 1 heart attack.The Rebif (beta-1a) did very little to help me. The medical team did even less. After roughly five unending years of trauma in the family my MS developed into progressive. There have been many changes in the last 3 to 4 years. Many falls, many fractured bones, and three moves all in five years. I have gone downhill. Considerably. We tried every shot available but nothing was working. There has been little if any progress in finding a reliable treatment for Multiple Sclerosis, My care provider Dr Miller introduced me to Kycuyu Health Clinic & their MS herbal treatment. The treatment is a miracle! I Adhere anyone reading this to try natu
(November 11, 2018)
My grandfather has had Ms for over 30 years so this cause is a very significant one in all of ours lives in my family.
(January 17, 2018)
I have two family members with MS and have donated to the organization before. I believe strongly in the mission of this association and want others to believe in it, too.
(November 26, 2017)
Because I want others to have as much fun as I will by going to this opportunity
(October 27, 2017)
I want draw attention to this important issue. I want to support as soon as I can. We all deserve a healthy life. I want to do something when I am healthy today.
(September 28, 2017)
It's a good thing to doand help people that need it looking forward to learning more about this hoping to #SD 100 class with this volunteer work so please contact me know what else I can do and how else I can help anyone that has to do with the situation thank you very much when it was to women for me
(June 7, 2017)
its an activity to have fun and raise money so im going to recommend this to all my friends to make more people come to the fundraiser
(May 3, 2017)
Completely available when needed
(January 3, 2017)
Multiple sclerosis is a deadly disease that affects the lives of many. My uncle has ALS and I wanted to help spread the word about similar diseases.
(November 22, 2016)
medical limitations/complications
(October 5, 2016)
i would refer this to a friend or a colleague because this is a great way to meet new people and also to help people
(August 30, 2016)
I want to help by donating my time in raiseing awareness for MSAA and collecting up donations.
(August 21, 2016)
It's good to help out organizations that strive for the better of the people and helping to prevent bad things from happening.
(July 31, 2016)
It was life changing for me.
(May 11, 2016)
any way to give back and help out is a positive step on path to happiness
(April 11, 2016)
Seems like a great organization
(December 15, 2015)
As a high school student at Fairfield Central High School, I want to get more involved in the community. I feel it is good to start volunteering at a young age because colleges and career opportunities will view you as a good candidate to join them. I encourage my friends to do the same.
(November 22, 2015)
The MSAA is a great place to spend time advocating for such a group that's commonly overlooked. Creating some sort of awareness itself and the question of, "What is Multiple Sclerosis?" was more than enough for me to see that the work of volunteers matter.
(July 24, 2015)
This organization is very flexible. Basically, you swim either individually or for a formed team and you swim! That's it! You swim for a goal or for fun, representing your involvement in helping the MS community. Throughout however long you want, you donate and encourage friends and family members to donate too!
(April 16, 2015)
I just have one question. By posting on social media ten times (for one hour of service credits) will I be able to write that down for an hour of service for my school even though it is virtual? Please respond as soon as possible
(March 11, 2015)
It's a wonderful cause to help others
(December 14, 2014)
The times I have been in a place with this sight was great, I only had one thing tht happened baly and htat was I was never contacted back to see if I was still here to help voluteer with the site wiht what i was asked about and that was would I help with the law office at the Court House! I wanted to vey much there are may seniors here in Great Falls that have questions and I could have helped them. Jeanne Marie Wallace
(October 16, 2014)
Everyone should want to change the world for good and this organization allows you to do so.
(October 13, 2014)
it was hard for me to find information regarding how to utilize pools that participate with this program
(August 21, 2014)
This association is amazing a finding all different ways people can volunteer, and building awareness around MS.
(August 20, 2014)
The MS Association of America has to be the most heart wrenching, personal, and incredibly inspiring volunteer organization I have ever encountered.
(August 12, 2014)
I would tell friends/family about this organization because my dad has MS and it would be great to inform the people around him more about it and it would be great to see them get involved in things that have to do more with MS
(October 3, 2013)
I never done volunteering but i believe no one should suffer or hurt when others aren't. I've been through a lot in my child hood and i believe no one else should. I think this is a great opportunity for anybody or anyone because it teaches you respect and responsibility.You life shouldn't be a suffer. If your hurt try making some else feel better about themselves because one thing might change someone else life.
(September 6, 2013)
I'm good with people and I like to help people.
(March 9, 2011)
I was diagnosed with MS about 4 years ago. I would recommend this organization to a friend or colleague.
(February 21, 2011)
I am a High School student at The G Star School of Motion Picture & Television School of the Arts and I am looking for volunteer hours for Silver Star students. I love to swim and also am good with people. I feel that your organization will be a great opportunity for me to give back to my community and to those who are in need of support.
(February 17, 2011)
My Mother died of this disease shortly after I returned home from Viet Nam in 1970.I am retired and unemployable with back issues but would like to help.
(July 5, 2010)
I myself have MS, and as such I am considered "unemployable". I was an "over-the-road" trucker until I was diagnosed with MS in 2000. After that I felt like I had some type of contagious disease. This is due mostly because people don't know or understand MS. Not all MS patients are confined to a wheel chair I feel that people need educated on MS.
(September 6, 2009)
MSAA is a terrific cause and I would recommend it to anyone looking to volunteer.
(August 27, 2009)
My best friend and my mother-in-law have this. We are also testing my husband for it. Let's fight for a cure!
(May 16, 2009)
It is personal
(March 24, 2009)
Because my Daughter and myself have MS. We need all the help with this disease as possible...
(March 17, 2009)
MSAA appreciates the interest and support of all of our volunteers - especially during March - National MS Awareness Month.
(February 22, 2009)
My daughter was diagnosed in 1994 and I have personally seen the debilitating effects of this disease. I want to help. David S. Salesville, AR
(January 30, 2009)
My older brother got this disease and passed away when it finally destroyed his heart.
(October 17, 2008)
cause i have ms and this organization helps people like me
(June 12, 2008)
I know many people who have interest as well
Previously Flagged and Approved