Hi I'm wondering is there anyone out there that could help me with my research. I have ms I'm 25 year old male. They are unsure as to which particular type I have they said PPMS first now they think it's RRMS. I was on copaxone for a short few months as I was not benefiting from it. I have been on LDN since 9 weeks after I was diagnosed. I'm still working full time I do the gym very regularly and I feel good except for the twitching the tightness in my knees and calves and ankles.
I have been doing so much research on MS and I have taken control of my body and I feel I'm extremely in touch with differences that occur in my body. I came across the HSCT treatment and I'm extremely interested I have read all the blogs and articles and journals however if I could chat with some one perhaps in Ireland that May have had it done that would be fantastic. I have fought very hard to get where I am in life and by hell or by crook il not let MS get in the way of my plans. I think there is no point moaning about my symptoms so I just get on with it. But if this treatment could work it would eradicate all my problems in terms of stopping the progression. I am aware that the treatment cannot be done in Ireland and I am in the process of sending my I for to Germany to let the prof check it out. I did find gerogegoss website absolutely excellent and informative. If anyone could give me a little info on anyone from Ireland treated with this therapy I would greatly appreciate it. Thanks.
Hsct patients in Ireland
Discuss stem cells, adult and embryonic, and their therapeutic potential for MS here.
Jump to
- Multiple Sclerosis
- ↳ General Discussion
- ↳ Introductions
- ↳ Drug Pipeline
- ↳ Regimens
- ↳ Undiagnosed
- ↳ MS Etiology and Pathogenesis
- Treatments
- ↳ Chronic Cerebrospinal Venous Insufficiency (CCSVI)
- ↳ Low Dose Naltrexone
- ↳ Tysabri (Antegren, Natalizumab)
- ↳ Copaxone
- ↳ Glatopa
- ↳ Avonex
- ↳ Rebif
- ↳ Betaseron
- ↳ Plegridy
- ↳ Novantrone
- ↳ Aimspro
- ↳ Diet
- ↳ Stem Cells
- ↳ Antibiotics
- ↳ Campath (Lemtrada, Alemtuzumab)
- ↳ Gene Therapy
- ↳ Natural Approach
- ↳ Biotin (Qizenday, Cerenday, MD1003)
- ↳ Coimbra High-Dose Vitamin D Protocol
- ↳ Statins
- ↳ Tcelna (Tovaxin)
- ↳ Revimmune (Cyclophosphamide, Cytoxan)
- ↳ Medical Devices
- ↳ Rituxan (Rituximab)
- ↳ Ocrevus (Ocrelizumab)
- ↳ Kesimpta (Ofatumumab)
- ↳ Briumvi (Ublituximab-xiiy)
- ↳ General Medications
- ↳ Tecfidera (BG-12, Dimethyl fumarate)
- ↳ Vumerity (Diroximel fumarate)
- ↳ Bafiertam (Monomethyl fumarate)
- ↳ Gilenya
- ↳ Aubagio (Teriflunomide)
- ↳ Mayzent (Siponimod)
- ↳ Zeposia (Ozanimod)
- ↳ Ponvory (Ponesimod)
- ↳ Mavenclad (Cladribine)
- ↳ Ampyra (Dalfampridine)
- ↳ Medical Marijuana
- ↳ Sativex
- ↳ Chiropractic Treatment
- Life
- ↳ Daily Life
- ↳ Veterans and MS
- ↳ Trigeminal Neuralgia in MS
- ↳ Reading Nook
- ↳ Humor
- ↳ Shopping
- ↳ Friends and Family
- ↳ Mental & Spiritual Health
- ↳ Exercise and Physical Therapy
- ↳ Under 25 with MS
- ↳ MS in the Golden Years
- ↳ Parenting Kids With MS
- ↳ Parents with MS
- ThisIsMS.com
- ↳ Site Support
- ↳ Suggestions